TY  - JOUR
AU  - Stefanović, Ivan
AU  - Džunuzović, Jasna
AU  - Džunuzović, Enis
AU  - Dapčević, Aleksandra
AU  - Šešlija, Sanja
AU  - Balanč, Bojana
AU  - Dobrzyńska-Mizera, Monika
PY  - 2021
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4
AB  - This work was focused on the synthesis of polyurethane networks (PUNs) based on polycaprolactone (PCL) as soft segment (SS) and Boltorn (R) aliphatic hyperbranched polyester of the second pseudo generation and 4,4 '-diphenylmethane diisocyanate (MDI) as the parts of the hard segments (HS), by a two-step solution polymerization. In order to find the best ratio between HS and SS to achieve good thermal and mechanical properties, suitable hydrophobicity and morphology of the PUNs, various experimental analyses were conducted. The obtained results revealed that features of the PUNs highly depend on the PCL content. The increase in the PCL content leads to the increase in thermal stability, hydrophobicity and appearance of the microphase separation, but on the other side, it also leads to the decrease in storage modulus in the rubbery plateau, crosslinking density and glass transition temperatures of PUNs. This work shows that features of PUNs can be easily adjusted for a specific application by careful selection of the SS and HS ratio.
PB  - Springer, New York
T2  - Polymer Bulletin
T1  - Composition-property relationship of polyurethane networks based on polycaprolactone diol
EP  - 7128
SP  - 7103
VL  - 78
DO  - 10.1007/s00289-020-03473-0
ER  - 

@article{
author = "Stefanović, Ivan and Džunuzović, Jasna and Džunuzović, Enis and Dapčević, Aleksandra and Šešlija, Sanja and Balanč, Bojana and Dobrzyńska-Mizera, Monika",
year = "2021",
abstract = "This work was focused on the synthesis of polyurethane networks (PUNs) based on polycaprolactone (PCL) as soft segment (SS) and Boltorn (R) aliphatic hyperbranched polyester of the second pseudo generation and 4,4 '-diphenylmethane diisocyanate (MDI) as the parts of the hard segments (HS), by a two-step solution polymerization. In order to find the best ratio between HS and SS to achieve good thermal and mechanical properties, suitable hydrophobicity and morphology of the PUNs, various experimental analyses were conducted. The obtained results revealed that features of the PUNs highly depend on the PCL content. The increase in the PCL content leads to the increase in thermal stability, hydrophobicity and appearance of the microphase separation, but on the other side, it also leads to the decrease in storage modulus in the rubbery plateau, crosslinking density and glass transition temperatures of PUNs. This work shows that features of PUNs can be easily adjusted for a specific application by careful selection of the SS and HS ratio.",
publisher = "Springer, New York",
journal = "Polymer Bulletin",
title = "Composition-property relationship of polyurethane networks based on polycaprolactone diol",
pages = "7128-7103",
volume = "78",
doi = "10.1007/s00289-020-03473-0"
}

Stefanović, I., Džunuzović, J., Džunuzović, E., Dapčević, A., Šešlija, S., Balanč, B.,& Dobrzyńska-Mizera, M.. (2021). Composition-property relationship of polyurethane networks based on polycaprolactone diol. in Polymer Bulletin
Springer, New York., 78, 7103-7128.
https://doi.org/10.1007/s00289-020-03473-0

Stefanović I, Džunuzović J, Džunuzović E, Dapčević A, Šešlija S, Balanč B, Dobrzyńska-Mizera M. Composition-property relationship of polyurethane networks based on polycaprolactone diol. in Polymer Bulletin. 2021;78:7103-7128.
doi:10.1007/s00289-020-03473-0 .

Stefanović, Ivan, Džunuzović, Jasna, Džunuzović, Enis, Dapčević, Aleksandra, Šešlija, Sanja, Balanč, Bojana, Dobrzyńska-Mizera, Monika, "Composition-property relationship of polyurethane networks based on polycaprolactone diol" in Polymer Bulletin, 78 (2021):7103-7128,
https://doi.org/10.1007/s00289-020-03473-0 . .

TY  - JOUR
AU  - Lazić, Anita M.
AU  - Radovanović, Lidija D.
AU  - Božić, Bojan Đ.
AU  - Božić Nedeljković, Biljana Đ.
AU  - Vitnik, Vesna D.
AU  - Vitnik, Željko J.
AU  - Rogan, Jelena R.
AU  - Valentić, Nataša V.
AU  - Ušćumlić, Gordana S.
AU  - Trišović, Nemanja P.
PY  - 2019
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4324
AB  - Two series of cycloalkanespiro-5-hydantoins, namely cyclo-hexanespiro-5-hydantoins and cycloheptanespiro-5-hydantoins with a 4-substituted benzyl or a 2-(4-substituted phenyl)-2-oxoethyl group at N3 position, were synthesized and their effects on proliferation of human colon (HCT-116), leukemia (K562) and breast (MDA-MB-231) cancer cell lines were tested. For comparison, we also described the 5,5-diphenylhydantoin analogues. The structural features of the investigated compounds were characterized by elemental analysis, FT-IR, UV-Vis, H-1 and C-13 NMR spectroscopy and X-ray crystallography. Regarding their structure-activity relationships, it was shown that the substitution on the benzyl moiety with the methoxy, chloro or bromo group potentiated the antiproliferative activity relative to the parent compounds, while an increase in the size of the cycloalkyl group resulted mostly in a decrease of the antiproliferative activity. The single crystal X-ray analysis revealed the existence of dimers and chains formed by the N-H center dot center dot center dot center dot O hydrogen bonds. The analysis of the molecular descriptors of Lipinski demonstrated that all investigated compounds obeyed the rule of five. To further understand their geometry and electronic structure, OFT calculations with B3LYP method using 6-311++G(d,p) basic set were performed. In this context, the UV-Vis spectra of the investigated compounds were analyzed in detail, whereby the predicted absorption spectra from DFT calculation matched the experimentally obtained ones, with a good correlation. The interesting physico-chemical and pharmacologically relevant properties of the investigated compounds warrant their further investigation.
PB  - Elsevier Science Bv, Amsterdam
T2  - Journal of Molecular Structure
T1  - Synthesis, structural characterization, DFT calculations and antiproliferative evaluation of novel spirohydantoin derivatives containing a substituted benzyl moiety
EP  - 62
SP  - 48
VL  - 1180
DO  - 10.1016/j.molstruc.2018.11.071
ER  - 

@article{
author = "Lazić, Anita M. and Radovanović, Lidija D. and Božić, Bojan Đ. and Božić Nedeljković, Biljana Đ. and Vitnik, Vesna D. and Vitnik, Željko J. and Rogan, Jelena R. and Valentić, Nataša V. and Ušćumlić, Gordana S. and Trišović, Nemanja P.",
year = "2019",
abstract = "Two series of cycloalkanespiro-5-hydantoins, namely cyclo-hexanespiro-5-hydantoins and cycloheptanespiro-5-hydantoins with a 4-substituted benzyl or a 2-(4-substituted phenyl)-2-oxoethyl group at N3 position, were synthesized and their effects on proliferation of human colon (HCT-116), leukemia (K562) and breast (MDA-MB-231) cancer cell lines were tested. For comparison, we also described the 5,5-diphenylhydantoin analogues. The structural features of the investigated compounds were characterized by elemental analysis, FT-IR, UV-Vis, H-1 and C-13 NMR spectroscopy and X-ray crystallography. Regarding their structure-activity relationships, it was shown that the substitution on the benzyl moiety with the methoxy, chloro or bromo group potentiated the antiproliferative activity relative to the parent compounds, while an increase in the size of the cycloalkyl group resulted mostly in a decrease of the antiproliferative activity. The single crystal X-ray analysis revealed the existence of dimers and chains formed by the N-H center dot center dot center dot center dot O hydrogen bonds. The analysis of the molecular descriptors of Lipinski demonstrated that all investigated compounds obeyed the rule of five. To further understand their geometry and electronic structure, OFT calculations with B3LYP method using 6-311++G(d,p) basic set were performed. In this context, the UV-Vis spectra of the investigated compounds were analyzed in detail, whereby the predicted absorption spectra from DFT calculation matched the experimentally obtained ones, with a good correlation. The interesting physico-chemical and pharmacologically relevant properties of the investigated compounds warrant their further investigation.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Journal of Molecular Structure",
title = "Synthesis, structural characterization, DFT calculations and antiproliferative evaluation of novel spirohydantoin derivatives containing a substituted benzyl moiety",
pages = "62-48",
volume = "1180",
doi = "10.1016/j.molstruc.2018.11.071"
}

Lazić, A. M., Radovanović, L. D., Božić, B. Đ., Božić Nedeljković, B. Đ., Vitnik, V. D., Vitnik, Ž. J., Rogan, J. R., Valentić, N. V., Ušćumlić, G. S.,& Trišović, N. P.. (2019). Synthesis, structural characterization, DFT calculations and antiproliferative evaluation of novel spirohydantoin derivatives containing a substituted benzyl moiety. in Journal of Molecular Structure
Elsevier Science Bv, Amsterdam., 1180, 48-62.
https://doi.org/10.1016/j.molstruc.2018.11.071

Lazić AM, Radovanović LD, Božić BĐ, Božić Nedeljković BĐ, Vitnik VD, Vitnik ŽJ, Rogan JR, Valentić NV, Ušćumlić GS, Trišović NP. Synthesis, structural characterization, DFT calculations and antiproliferative evaluation of novel spirohydantoin derivatives containing a substituted benzyl moiety. in Journal of Molecular Structure. 2019;1180:48-62.
doi:10.1016/j.molstruc.2018.11.071 .

Lazić, Anita M., Radovanović, Lidija D., Božić, Bojan Đ., Božić Nedeljković, Biljana Đ., Vitnik, Vesna D., Vitnik, Željko J., Rogan, Jelena R., Valentić, Nataša V., Ušćumlić, Gordana S., Trišović, Nemanja P., "Synthesis, structural characterization, DFT calculations and antiproliferative evaluation of novel spirohydantoin derivatives containing a substituted benzyl moiety" in Journal of Molecular Structure, 1180 (2019):48-62,
https://doi.org/10.1016/j.molstruc.2018.11.071 . .

TY  - CONF
AU  - Radovanović, Lidija
AU  - Dapčević, Aleksandra
AU  - Rogan, Jelena
PY  - 2019
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6703
AB  - Reakcijom izmene liganada različitim metodama sinteze dobijeno je 22 ternarna
kompleksa elemenata d-bloka [Mn(II), Co(II), Ni(II), Cu(II) i Zn(II)] sa anjonima
aromatičnih polikarboksilnih kiselina (ftalne, izoftalne, tereftalne i piromelitne) kao
O,O-donorskim ligandima i aromatičnim N,N-donorskim ligandima kao što su
2,2'-dipiridilamin i 2,2'-bipirimidin [1–5]. Trinaest kompleksa sintetisano je u
monokristalnom obliku, dok su ostala jedinjenja mikrokristalna. Prema vrsti centralnog
atoma, u obliku monokristala dobijeno je pet Mn(II)-, dva Co(II)-, jedan Ni(II)-, dva
Cu(II)-, dva Zn(II)-kompleksa, kao i bimetalni Mn(II)–Cu(II)-kompleks. Kristalne
strukture ovih jedinjenja određene su rendgenskom strukturnom analizom. Strukturne
karakteristike kompleksa detaljno su opisane i međusobno su upoređene. Sintetisani
kompleksi ispitani su infracrvenom spektroskopijom (IC), a neki su dodatno podvrgnuti
kvantno-hemijskim proračunima, simultanoj termogravimetrijskoj, diferencijalnoj
termijskoj i diferencijalnoj skenirajućoj kalorimetrijskoj analizi (TG/DTA/DSC),
elementarnoj analizi, magnetnim merenjima na sobnoj i niskim temperaturama,
energetskoj disperzivnoj i atomskoj apsorpcionoj spektroskopiji (EDS i AAS) i merenju
fotoluminescencije. Za pojedine komplekse ispitana je i antimikrobna aktivnost. Na
osnovu rezultata IC-, ED- i AA-spektroskopije, elementarne i TG/DSC-analize,
magnetnih merenja i boje određene su formule mikrokristalnih kompleksa i
pretpostavljena je njihova struktura.
Kod kompleksa dobijenih u obliku monokristala razmatrani su parametri koji dovode
do strukturnih različitosti, kao što su dužine veza i uglovi, koordinacioni broj jona metala,
način koordinacije O,O- i N,N-donorskih liganada i uticaj nekovalentnih interakcija na
geometriju i pakovanje molekula [1–5]. Koordinacioni brojevi d-elemenata su različiti i
nalaze se u opsegu od 5 do 7. Kod većine kompleksa O,O-donorski ligandi imaju
mostovnu ulogu sa različitim načinima koordinacije COO–
-grupa, u rasponu od bis-
-monodentatnog do heksadentatnog vezivanja. Kod tri jedinjenja ovi ligandi nisu
koordinirani za jone metala, već učestvuju u građenju vodoničnih veza. Dobijeni
kompleksi su mononuklearni, binuklearni i polimerni, a supramolekulsko 3D
umrežavanje postiže se vodoničnim vezama i slabijim nekovalentnim interakcijama
(C–Hꞏꞏꞏπ, π-π, C–HꞏꞏꞏN i C–HꞏꞏꞏO) između 1D lanaca ili 2D slojeva.
Pretragom Kembričke kristalografske baze podataka utvrđene su orijentacije
COO–
-grupa kod benzen-dikarboksilat kompleksa [1]. Energije tri poziciona izomera
benzen-dikarboksilat-jona izračunate su pomoću Møller-Plesset perturbacione teorije drugog reda i tri hibridne HF/DFT metode sa 6-311G** baznim setom. Rezultati analiza
dekompozicije lokalnih molekulskih orbitala i prirodnih vezujućih orbitala pokazali su
odlično slaganje eksperimentalne i izračunate geometrije, čime je dokazano da je
planarna konformacija energetski najpovoljnija kod anjona tereftalne i izoftalne kiseline,
dok su kod anjona ftalne kiseline COO–
-grupe zarotirane i formiraju komplementarne
uglove u odnosu na benzenski prsten u najstabilnijoj konformaciji.
Termička stabilnost, magnetna, fotoluminescentna svojstva i antimikrobna aktivnost
pojedinih kompleksa detaljno su analizirani i povezani sa njihovim strukturnim
karakteristikama. Merenja magnetne susceptibilnosti pokazala su da većina ispitanih
kompleksa ima paramagnetna svojstva, sa izuzetkom jednog Co(II)-kompleksa kod kojeg
su nađene feromagnetne interakcije, što je dovedeno u vezu sa formiranjem lanaca
između molekula u kristalnom pakovanju. Ispitivanja fotoluminescencije
Zn(II)-kompleksa pokazala su da su ovi kompleksi optički aktivni, s tim da je najjači
intenzitet fotoluminescencije utvrđen za kompleks kod kojeg postoji veći broj
nekovalentnih interakcija u strukturi. Antimikrobna svojstva Zn(II)-kompleksa ispitana
su in vitro na Gram-pozitivne bakterije (Bacilus subtilis, Enterococcus faecalis, Listeria
monocytogenes i Staphylococcus aureus), Gram-negativne bakterije (Esherichia coli,
Pseudomonas aeruginosa i Salmonella enteritidis) i gljivicu Candida albicans i pokazano
je da Zn(II)-kompleks sa izoftalat-jonom ima najbolju aktivnost na bakterije Listeria
monocytogenes i Esherichia coli [2]. Diskutovana je veza između antimikrobne
aktivnosti kompleksa i njihovih kristalnih struktura.
AB  - A series of 22 d-block element complexes [Mn(II), Co(II), Ni(II), Cu(II) and Zn(II)]
containing anions of aromatic polycarboxylate acids (phthalic, isophthalic, terephthalic
and pyromellic) as O,O-donor ligands and aromatic N,N-donor ligands such as
2,2'-dipyridylamine and 2,2'-bipyrimidine, has been obtained by ligand exchange reaction
using different synthetic methods [1–5]. Thirteen complexes were obtained as single
crystals, while the others were microcrystalline. According to the type of central atom,
five Mn(II), two Co(II), one Ni(II), two Cu(II), two Zn(II) complexes, and bimetallic
Mn(II)–Cu(II) complex were synthesized in form of single crystals. The structures of
these compounds were determined by single-crystal X-ray analysis. Structural properties
of complexes were discussed in detail and compared. All complexes were characterized
by infrared (IR) spectroscopy, while some of them were also subjected to the quantumchemical calculations, simultaneous thermogravimetry, differential thermal analysis and
differential scanning calorimetry (TG/DTA/DSC analysis), elemental analysis, magnetic
measurements at room and low temperatures, energy-dispersive X-ray spectroscopy
(EDS), atomic absorption spectroscopy (AAS) and photoluminescence measurements.
Antimicrobial activity was also investigated for some complexes. Based on the results of
IR, EDS and AAS spectroscopy, elemental and TG/DSC analyses, magnetic
measurements and color, the formulae of microcrystalline complexes were determined
and the structures were assumed.
The parameters that affect structural diversities, such as bond lengths and angles, the
coordination number of metal ions, the coordination mode of O,O- and
N,N-donor ligands and the influence of non-covalent interactions on geometry and crystal
packing were considered for the complexes in form of single crystals [1–5]. The
coordination numbers of d-elements are different and range from 5 to 7. In most of
compounds, O,O-donor ligands have the bridging role with different coordination modes
of COO–
 groups, i.e. from bis monodentate to hexadentate. These ligands are counter ions
only in three compounds and are involved in the hydrogen bonds. The complexes are
mononuclear, binuclear and polymeric, and supramolecular 3D networking is achieved
by hydrogen bonds and weak non-covalent interactions (C–Hꞏꞏꞏπ, π-π, C–HꞏꞏꞏN and
C–HꞏꞏꞏO) between 1D chains or 2D layers.
Based on search of the Cambridge Structural Database, the orientations of COO–
groups in benzenedicarboxylate complexes were determined [1]. The energies of three
positional isomers of benzenedicarboxylate ions were calculated using the second-order Møller-Plesset perturbation theory and three hybrid HF/DFT methods with 6-311G**
basis set. Results of Localized Molecular Orbital Energy Decomposition and Natural
Bond Orbital analyses have shown that experimental and calculated geometries are in
agreement, indicating that the terephthalate and isophthalate anions prefer the planar
conformation, while COO–
 groups are inclined and make complementary angles relative
to the aromatic rings in the phthalate anions.
Thermal stability, magnetic, photoluminescent and antimicrobial properties of some
complexes have been analyzed in detail and correlated with their structural features.
Magnetic susceptibility measurements have shown that the most of complexes exhibit
paramagnetic behavior, with the exception of one ferromagnetic Co(II) complex, which is
related to the formation of chains between molecules in the crystal packing. The
photoluminescence investigation has shown the optical activity of Zn(II) complexes with
the strongest intensity of photoluminescence for the complex with the increased number
of noncovalent interactions in structure. The antimicrobial behaviour of Zn(II) complexes
were tested in vitro against Gram-positive bacteria (Bacilus subtilis, Enterococcus
faecalis, Listeria monocytogenes and Staphylococcus aureus), Gram-negative bacteria
(Esherichia coli, Pseudomonas aeruginosa and Salmonella enteritidis) and yiest Candida
albicans and it has been shown that Zn(II) complex with isophthalate ion exhibited the
best activity against Listeria monocytogenes and Esherichia coli [2]. The relationship
between the antimicrobial behavior of complexes and their crystal structures is discussed.
PB  - Beograd : Srpsko kristalografsko društvo
C3  - Izvodi radova / XXVI konferencija Srpskog kristalografskog društva, Srebrno jezero, 27–28. jun 2019
T1  - KOMPLEKSI ELEMENATA d-BLOKA SA AROMATIČNIM O,O- I N,N-DONORSKIM LIGANDIMA: SINTEZA, STRUKTURA, SVOJSTVA I PRIMENA
T1  - COMPLEXES OF d-BLOCK ELEMENTS WITH AROMATIC O,O- AND N,N-DONOR LIGANDS: SYNTHESIS, STRUCTURE, PROPERTIES AND APPLICATIONS
EP  - 14
SP  - 11
UR  - https://hdl.handle.net/21.15107/rcub_technorep_6703
ER  - 

@conference{
author = "Radovanović, Lidija and Dapčević, Aleksandra and Rogan, Jelena",
year = "2019",
abstract = "Reakcijom izmene liganada različitim metodama sinteze dobijeno je 22 ternarna
kompleksa elemenata d-bloka [Mn(II), Co(II), Ni(II), Cu(II) i Zn(II)] sa anjonima
aromatičnih polikarboksilnih kiselina (ftalne, izoftalne, tereftalne i piromelitne) kao
O,O-donorskim ligandima i aromatičnim N,N-donorskim ligandima kao što su
2,2'-dipiridilamin i 2,2'-bipirimidin [1–5]. Trinaest kompleksa sintetisano je u
monokristalnom obliku, dok su ostala jedinjenja mikrokristalna. Prema vrsti centralnog
atoma, u obliku monokristala dobijeno je pet Mn(II)-, dva Co(II)-, jedan Ni(II)-, dva
Cu(II)-, dva Zn(II)-kompleksa, kao i bimetalni Mn(II)–Cu(II)-kompleks. Kristalne
strukture ovih jedinjenja određene su rendgenskom strukturnom analizom. Strukturne
karakteristike kompleksa detaljno su opisane i međusobno su upoređene. Sintetisani
kompleksi ispitani su infracrvenom spektroskopijom (IC), a neki su dodatno podvrgnuti
kvantno-hemijskim proračunima, simultanoj termogravimetrijskoj, diferencijalnoj
termijskoj i diferencijalnoj skenirajućoj kalorimetrijskoj analizi (TG/DTA/DSC),
elementarnoj analizi, magnetnim merenjima na sobnoj i niskim temperaturama,
energetskoj disperzivnoj i atomskoj apsorpcionoj spektroskopiji (EDS i AAS) i merenju
fotoluminescencije. Za pojedine komplekse ispitana je i antimikrobna aktivnost. Na
osnovu rezultata IC-, ED- i AA-spektroskopije, elementarne i TG/DSC-analize,
magnetnih merenja i boje određene su formule mikrokristalnih kompleksa i
pretpostavljena je njihova struktura.
Kod kompleksa dobijenih u obliku monokristala razmatrani su parametri koji dovode
do strukturnih različitosti, kao što su dužine veza i uglovi, koordinacioni broj jona metala,
način koordinacije O,O- i N,N-donorskih liganada i uticaj nekovalentnih interakcija na
geometriju i pakovanje molekula [1–5]. Koordinacioni brojevi d-elemenata su različiti i
nalaze se u opsegu od 5 do 7. Kod većine kompleksa O,O-donorski ligandi imaju
mostovnu ulogu sa različitim načinima koordinacije COO–
-grupa, u rasponu od bis-
-monodentatnog do heksadentatnog vezivanja. Kod tri jedinjenja ovi ligandi nisu
koordinirani za jone metala, već učestvuju u građenju vodoničnih veza. Dobijeni
kompleksi su mononuklearni, binuklearni i polimerni, a supramolekulsko 3D
umrežavanje postiže se vodoničnim vezama i slabijim nekovalentnim interakcijama
(C–Hꞏꞏꞏπ, π-π, C–HꞏꞏꞏN i C–HꞏꞏꞏO) između 1D lanaca ili 2D slojeva.
Pretragom Kembričke kristalografske baze podataka utvrđene su orijentacije
COO–
-grupa kod benzen-dikarboksilat kompleksa [1]. Energije tri poziciona izomera
benzen-dikarboksilat-jona izračunate su pomoću Møller-Plesset perturbacione teorije drugog reda i tri hibridne HF/DFT metode sa 6-311G** baznim setom. Rezultati analiza
dekompozicije lokalnih molekulskih orbitala i prirodnih vezujućih orbitala pokazali su
odlično slaganje eksperimentalne i izračunate geometrije, čime je dokazano da je
planarna konformacija energetski najpovoljnija kod anjona tereftalne i izoftalne kiseline,
dok su kod anjona ftalne kiseline COO–
-grupe zarotirane i formiraju komplementarne
uglove u odnosu na benzenski prsten u najstabilnijoj konformaciji.
Termička stabilnost, magnetna, fotoluminescentna svojstva i antimikrobna aktivnost
pojedinih kompleksa detaljno su analizirani i povezani sa njihovim strukturnim
karakteristikama. Merenja magnetne susceptibilnosti pokazala su da većina ispitanih
kompleksa ima paramagnetna svojstva, sa izuzetkom jednog Co(II)-kompleksa kod kojeg
su nađene feromagnetne interakcije, što je dovedeno u vezu sa formiranjem lanaca
između molekula u kristalnom pakovanju. Ispitivanja fotoluminescencije
Zn(II)-kompleksa pokazala su da su ovi kompleksi optički aktivni, s tim da je najjači
intenzitet fotoluminescencije utvrđen za kompleks kod kojeg postoji veći broj
nekovalentnih interakcija u strukturi. Antimikrobna svojstva Zn(II)-kompleksa ispitana
su in vitro na Gram-pozitivne bakterije (Bacilus subtilis, Enterococcus faecalis, Listeria
monocytogenes i Staphylococcus aureus), Gram-negativne bakterije (Esherichia coli,
Pseudomonas aeruginosa i Salmonella enteritidis) i gljivicu Candida albicans i pokazano
je da Zn(II)-kompleks sa izoftalat-jonom ima najbolju aktivnost na bakterije Listeria
monocytogenes i Esherichia coli [2]. Diskutovana je veza između antimikrobne
aktivnosti kompleksa i njihovih kristalnih struktura., A series of 22 d-block element complexes [Mn(II), Co(II), Ni(II), Cu(II) and Zn(II)]
containing anions of aromatic polycarboxylate acids (phthalic, isophthalic, terephthalic
and pyromellic) as O,O-donor ligands and aromatic N,N-donor ligands such as
2,2'-dipyridylamine and 2,2'-bipyrimidine, has been obtained by ligand exchange reaction
using different synthetic methods [1–5]. Thirteen complexes were obtained as single
crystals, while the others were microcrystalline. According to the type of central atom,
five Mn(II), two Co(II), one Ni(II), two Cu(II), two Zn(II) complexes, and bimetallic
Mn(II)–Cu(II) complex were synthesized in form of single crystals. The structures of
these compounds were determined by single-crystal X-ray analysis. Structural properties
of complexes were discussed in detail and compared. All complexes were characterized
by infrared (IR) spectroscopy, while some of them were also subjected to the quantumchemical calculations, simultaneous thermogravimetry, differential thermal analysis and
differential scanning calorimetry (TG/DTA/DSC analysis), elemental analysis, magnetic
measurements at room and low temperatures, energy-dispersive X-ray spectroscopy
(EDS), atomic absorption spectroscopy (AAS) and photoluminescence measurements.
Antimicrobial activity was also investigated for some complexes. Based on the results of
IR, EDS and AAS spectroscopy, elemental and TG/DSC analyses, magnetic
measurements and color, the formulae of microcrystalline complexes were determined
and the structures were assumed.
The parameters that affect structural diversities, such as bond lengths and angles, the
coordination number of metal ions, the coordination mode of O,O- and
N,N-donor ligands and the influence of non-covalent interactions on geometry and crystal
packing were considered for the complexes in form of single crystals [1–5]. The
coordination numbers of d-elements are different and range from 5 to 7. In most of
compounds, O,O-donor ligands have the bridging role with different coordination modes
of COO–
 groups, i.e. from bis monodentate to hexadentate. These ligands are counter ions
only in three compounds and are involved in the hydrogen bonds. The complexes are
mononuclear, binuclear and polymeric, and supramolecular 3D networking is achieved
by hydrogen bonds and weak non-covalent interactions (C–Hꞏꞏꞏπ, π-π, C–HꞏꞏꞏN and
C–HꞏꞏꞏO) between 1D chains or 2D layers.
Based on search of the Cambridge Structural Database, the orientations of COO–
groups in benzenedicarboxylate complexes were determined [1]. The energies of three
positional isomers of benzenedicarboxylate ions were calculated using the second-order Møller-Plesset perturbation theory and three hybrid HF/DFT methods with 6-311G**
basis set. Results of Localized Molecular Orbital Energy Decomposition and Natural
Bond Orbital analyses have shown that experimental and calculated geometries are in
agreement, indicating that the terephthalate and isophthalate anions prefer the planar
conformation, while COO–
 groups are inclined and make complementary angles relative
to the aromatic rings in the phthalate anions.
Thermal stability, magnetic, photoluminescent and antimicrobial properties of some
complexes have been analyzed in detail and correlated with their structural features.
Magnetic susceptibility measurements have shown that the most of complexes exhibit
paramagnetic behavior, with the exception of one ferromagnetic Co(II) complex, which is
related to the formation of chains between molecules in the crystal packing. The
photoluminescence investigation has shown the optical activity of Zn(II) complexes with
the strongest intensity of photoluminescence for the complex with the increased number
of noncovalent interactions in structure. The antimicrobial behaviour of Zn(II) complexes
were tested in vitro against Gram-positive bacteria (Bacilus subtilis, Enterococcus
faecalis, Listeria monocytogenes and Staphylococcus aureus), Gram-negative bacteria
(Esherichia coli, Pseudomonas aeruginosa and Salmonella enteritidis) and yiest Candida
albicans and it has been shown that Zn(II) complex with isophthalate ion exhibited the
best activity against Listeria monocytogenes and Esherichia coli [2]. The relationship
between the antimicrobial behavior of complexes and their crystal structures is discussed.",
publisher = "Beograd : Srpsko kristalografsko društvo",
journal = "Izvodi radova / XXVI konferencija Srpskog kristalografskog društva, Srebrno jezero, 27–28. jun 2019",
title = "KOMPLEKSI ELEMENATA d-BLOKA SA AROMATIČNIM O,O- I N,N-DONORSKIM LIGANDIMA: SINTEZA, STRUKTURA, SVOJSTVA I PRIMENA, COMPLEXES OF d-BLOCK ELEMENTS WITH AROMATIC O,O- AND N,N-DONOR LIGANDS: SYNTHESIS, STRUCTURE, PROPERTIES AND APPLICATIONS",
pages = "14-11",
url = "https://hdl.handle.net/21.15107/rcub_technorep_6703"
}

Radovanović, L., Dapčević, A.,& Rogan, J.. (2019). KOMPLEKSI ELEMENATA d-BLOKA SA AROMATIČNIM O,O- I N,N-DONORSKIM LIGANDIMA: SINTEZA, STRUKTURA, SVOJSTVA I PRIMENA. in Izvodi radova / XXVI konferencija Srpskog kristalografskog društva, Srebrno jezero, 27–28. jun 2019
Beograd : Srpsko kristalografsko društvo., 11-14.
https://hdl.handle.net/21.15107/rcub_technorep_6703

Radovanović L, Dapčević A, Rogan J. KOMPLEKSI ELEMENATA d-BLOKA SA AROMATIČNIM O,O- I N,N-DONORSKIM LIGANDIMA: SINTEZA, STRUKTURA, SVOJSTVA I PRIMENA. in Izvodi radova / XXVI konferencija Srpskog kristalografskog društva, Srebrno jezero, 27–28. jun 2019. 2019;:11-14.
https://hdl.handle.net/21.15107/rcub_technorep_6703 .

Radovanović, Lidija, Dapčević, Aleksandra, Rogan, Jelena, "KOMPLEKSI ELEMENATA d-BLOKA SA AROMATIČNIM O,O- I N,N-DONORSKIM LIGANDIMA: SINTEZA, STRUKTURA, SVOJSTVA I PRIMENA" in Izvodi radova / XXVI konferencija Srpskog kristalografskog društva, Srebrno jezero, 27–28. jun 2019 (2019):11-14,
https://hdl.handle.net/21.15107/rcub_technorep_6703 .

TY  - CONF
AU  - Radovanović, Lidija
AU  - Vulić, Predrag
AU  - Radovanović, Željko
AU  - Rogan, Jelena
PY  - 2019
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6721
AB  - Development of nanomaterials such as transition metal oxides with spinel
structure has been intensively examined because of their applications in catalysis,
energy storage, magnetic data storage and sensors [1]. Synthesis of these materials
has been realized by various approaches, such as hydrothermal synthesis, solid state
reactions and microwave synthesis [1]. In previous years, thermolysis of transition
metal complexes as precursors provides a new technique in preparing useful
nanomaterials due to the possibility to control their particle size and morphology [2].
The nano- and microparticles of Co3O4 have been prepared by direct calcination
of ternary Co(II) complex, [Co3(bipym)3(H3mell)2]·18H2O, where bipym is
2,2’-bipyrimidine and H3mell3–
is anion of 1,2,3,4,5,6-benzenehexacarboxylic
(mellitic) acid at 450 and 1000 °C in air atmosphere. The powder X-ray diffraction
(XRDP) and scanning electron microscopy (SEM) were used to investigate structure
and morphology of the obtained materials. The results indicated the formation of
pure Co3O4 phase, whose particles size depends on the calcination temperature.
PB  - Belgrade : Institute for Multidisciplinary Research, University
C3  - Programme and the Book of Abstracts / 5th Conference of The Serbian Society for Ceramic Materials, 5CSCS-2019, June 11-13, 2019, Belgrade, Serbia
T1  - Preparation Co3O4 nano- and microparticles by solid state thermolysis of cobalt(II) complex
SP  - 92
UR  - https://hdl.handle.net/21.15107/rcub_technorep_6721
ER  - 

@conference{
author = "Radovanović, Lidija and Vulić, Predrag and Radovanović, Željko and Rogan, Jelena",
year = "2019",
abstract = "Development of nanomaterials such as transition metal oxides with spinel
structure has been intensively examined because of their applications in catalysis,
energy storage, magnetic data storage and sensors [1]. Synthesis of these materials
has been realized by various approaches, such as hydrothermal synthesis, solid state
reactions and microwave synthesis [1]. In previous years, thermolysis of transition
metal complexes as precursors provides a new technique in preparing useful
nanomaterials due to the possibility to control their particle size and morphology [2].
The nano- and microparticles of Co3O4 have been prepared by direct calcination
of ternary Co(II) complex, [Co3(bipym)3(H3mell)2]·18H2O, where bipym is
2,2’-bipyrimidine and H3mell3–
is anion of 1,2,3,4,5,6-benzenehexacarboxylic
(mellitic) acid at 450 and 1000 °C in air atmosphere. The powder X-ray diffraction
(XRDP) and scanning electron microscopy (SEM) were used to investigate structure
and morphology of the obtained materials. The results indicated the formation of
pure Co3O4 phase, whose particles size depends on the calcination temperature.",
publisher = "Belgrade : Institute for Multidisciplinary Research, University",
journal = "Programme and the Book of Abstracts / 5th Conference of The Serbian Society for Ceramic Materials, 5CSCS-2019, June 11-13, 2019, Belgrade, Serbia",
title = "Preparation Co3O4 nano- and microparticles by solid state thermolysis of cobalt(II) complex",
pages = "92",
url = "https://hdl.handle.net/21.15107/rcub_technorep_6721"
}

Radovanović, L., Vulić, P., Radovanović, Ž.,& Rogan, J.. (2019). Preparation Co3O4 nano- and microparticles by solid state thermolysis of cobalt(II) complex. in Programme and the Book of Abstracts / 5th Conference of The Serbian Society for Ceramic Materials, 5CSCS-2019, June 11-13, 2019, Belgrade, Serbia
Belgrade : Institute for Multidisciplinary Research, University., 92.
https://hdl.handle.net/21.15107/rcub_technorep_6721

Radovanović L, Vulić P, Radovanović Ž, Rogan J. Preparation Co3O4 nano- and microparticles by solid state thermolysis of cobalt(II) complex. in Programme and the Book of Abstracts / 5th Conference of The Serbian Society for Ceramic Materials, 5CSCS-2019, June 11-13, 2019, Belgrade, Serbia. 2019;:92.
https://hdl.handle.net/21.15107/rcub_technorep_6721 .

Radovanović, Lidija, Vulić, Predrag, Radovanović, Željko, Rogan, Jelena, "Preparation Co3O4 nano- and microparticles by solid state thermolysis of cobalt(II) complex" in Programme and the Book of Abstracts / 5th Conference of The Serbian Society for Ceramic Materials, 5CSCS-2019, June 11-13, 2019, Belgrade, Serbia (2019):92,
https://hdl.handle.net/21.15107/rcub_technorep_6721 .

TY  - JOUR
AU  - Milovanović, Stoja
AU  - Đuriš, Jelena
AU  - Dapčević, Aleksandra
AU  - Medarević, Đorđe
AU  - Ibrić, Svetlana
AU  - Žižović, Irena
PY  - 2019
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4074
AB  - The present work is aimed towards designing advanced materials by means of sustainable processes. In that sense, the utilization of supercritical CO2 (scCO(2)) for processing of pharmaceutical polymers (Soluplus (R), Eudragit (R), and hydroxypropyl methylcellulose acetate succinate), alone and with an addition of cardiovascular drug Carvedilol, was explored. Employed single-step static scCO(2) process (pressure of 30 MPa and temperature of 100 degrees C for 2 h) enabled fabrication of solvent-free polymeric foams and Carvedilol solid dispersions with controlled microstructure and average pore diameter of 101-257 pm suitable for application in the pharmaceutical industry. ScCO2 did not remain in the foams after processing or affected the polymer composition, while Carvedilol formed hydrogen bonds with the polymers. Carvedilol was molecularly dispersed in the fabricated solid dispersions and its transition from the crystalline to amorphous form was complete. Korsmeyer-Peppas model was successfully used for the mathematical description of Carvedilol dissolution from solid dispersions. The dissolution rate of Carvedilol in acidic medium was significantly enhanced by its dispersion in tested polymers using the proposed high-pressure method.
PB  - Elsevier Sci Ltd, Oxford
T2  - Polymer Testing
T1  - Soluplus (R), Eudragit (R), HPMC-AS foams and solid dispersions for enhancement of Carvedilol dissolution rate prepared by a supercritical CO2 process
EP  - 64
SP  - 54
VL  - 76
DO  - 10.1016/j.polymertesting.2019.03.001
ER  - 

@article{
author = "Milovanović, Stoja and Đuriš, Jelena and Dapčević, Aleksandra and Medarević, Đorđe and Ibrić, Svetlana and Žižović, Irena",
year = "2019",
abstract = "The present work is aimed towards designing advanced materials by means of sustainable processes. In that sense, the utilization of supercritical CO2 (scCO(2)) for processing of pharmaceutical polymers (Soluplus (R), Eudragit (R), and hydroxypropyl methylcellulose acetate succinate), alone and with an addition of cardiovascular drug Carvedilol, was explored. Employed single-step static scCO(2) process (pressure of 30 MPa and temperature of 100 degrees C for 2 h) enabled fabrication of solvent-free polymeric foams and Carvedilol solid dispersions with controlled microstructure and average pore diameter of 101-257 pm suitable for application in the pharmaceutical industry. ScCO2 did not remain in the foams after processing or affected the polymer composition, while Carvedilol formed hydrogen bonds with the polymers. Carvedilol was molecularly dispersed in the fabricated solid dispersions and its transition from the crystalline to amorphous form was complete. Korsmeyer-Peppas model was successfully used for the mathematical description of Carvedilol dissolution from solid dispersions. The dissolution rate of Carvedilol in acidic medium was significantly enhanced by its dispersion in tested polymers using the proposed high-pressure method.",
publisher = "Elsevier Sci Ltd, Oxford",
journal = "Polymer Testing",
title = "Soluplus (R), Eudragit (R), HPMC-AS foams and solid dispersions for enhancement of Carvedilol dissolution rate prepared by a supercritical CO2 process",
pages = "64-54",
volume = "76",
doi = "10.1016/j.polymertesting.2019.03.001"
}

Milovanović, S., Đuriš, J., Dapčević, A., Medarević, Đ., Ibrić, S.,& Žižović, I.. (2019). Soluplus (R), Eudragit (R), HPMC-AS foams and solid dispersions for enhancement of Carvedilol dissolution rate prepared by a supercritical CO2 process. in Polymer Testing
Elsevier Sci Ltd, Oxford., 76, 54-64.
https://doi.org/10.1016/j.polymertesting.2019.03.001

Milovanović S, Đuriš J, Dapčević A, Medarević Đ, Ibrić S, Žižović I. Soluplus (R), Eudragit (R), HPMC-AS foams and solid dispersions for enhancement of Carvedilol dissolution rate prepared by a supercritical CO2 process. in Polymer Testing. 2019;76:54-64.
doi:10.1016/j.polymertesting.2019.03.001 .

Milovanović, Stoja, Đuriš, Jelena, Dapčević, Aleksandra, Medarević, Đorđe, Ibrić, Svetlana, Žižović, Irena, "Soluplus (R), Eudragit (R), HPMC-AS foams and solid dispersions for enhancement of Carvedilol dissolution rate prepared by a supercritical CO2 process" in Polymer Testing, 76 (2019):54-64,
https://doi.org/10.1016/j.polymertesting.2019.03.001 . .

TY  - JOUR
AU  - Luković-Golić, Danijela
AU  - Radojković, Aleksandar
AU  - Dapčević, Aleksandra
AU  - Pajić, Damir
AU  - Dragović, Jure
AU  - Torić, Filip
AU  - Ćirković, Jovana
AU  - Branković, Goran
AU  - Branković, Zorica
PY  - 2019
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4079
AB  - Bismuth ferrite, BiFeO3, was doped with a wide range of concentrations (0-30%) of Gd in order to investigate structural, ferroelectric, and magnetic properties and their correlation. Powder samples of Bi1-xGdxFeO3 (x = 0.00-0.30) were prepared using the hydro-evaporation synthesis method. Sintering process at 870 degrees C for 6 h of as-prepared, Gd doped BiFeO3 powders resulted in ceramic samples with relative densities in the range of (74-86) %. XRD analysis revealed that Bi1-xGdxFeO3 samples (x = 0.00-0.09) crystallized in rhombohedral phase; Bi1-xGdxFeO3 samples (x = 0.10-0.20) contained both rhombohedral and orthorhombic phases, while Bi1-xGdxFeO3 (x = 0.30) sample contained only the orthorhombic phase. The structural parameters obtained after Rietveld refinement for single-phase Bi1-xGdxFeO3 ceramic samples and microstructure image analysis were correlated with the results of ferroelectric and magnetic measurements. Bi1-xGdxFeO3 (x = 0.0625, 0.075, 0.09) samples showed improved ferroelectric properties and reduced leakage current density in comparison with undoped BiFeO3. Gradual increase in Gd content in BiFeO3 led to enhanced magnetic responses and weak ferromagnetic behavior.
PB  - Elsevier Sci Ltd, Oxford
T2  - Ceramics International
T1  - Change in structural, ferroelectric, and magnetic properties of bismuth ferrite induced by doping with gadolinium
EP  - 19165
IS  - 15
SP  - 19158
VL  - 45
DO  - 10.1016/j.ceramint.2019.06.162
ER  - 

@article{
author = "Luković-Golić, Danijela and Radojković, Aleksandar and Dapčević, Aleksandra and Pajić, Damir and Dragović, Jure and Torić, Filip and Ćirković, Jovana and Branković, Goran and Branković, Zorica",
year = "2019",
abstract = "Bismuth ferrite, BiFeO3, was doped with a wide range of concentrations (0-30%) of Gd in order to investigate structural, ferroelectric, and magnetic properties and their correlation. Powder samples of Bi1-xGdxFeO3 (x = 0.00-0.30) were prepared using the hydro-evaporation synthesis method. Sintering process at 870 degrees C for 6 h of as-prepared, Gd doped BiFeO3 powders resulted in ceramic samples with relative densities in the range of (74-86) %. XRD analysis revealed that Bi1-xGdxFeO3 samples (x = 0.00-0.09) crystallized in rhombohedral phase; Bi1-xGdxFeO3 samples (x = 0.10-0.20) contained both rhombohedral and orthorhombic phases, while Bi1-xGdxFeO3 (x = 0.30) sample contained only the orthorhombic phase. The structural parameters obtained after Rietveld refinement for single-phase Bi1-xGdxFeO3 ceramic samples and microstructure image analysis were correlated with the results of ferroelectric and magnetic measurements. Bi1-xGdxFeO3 (x = 0.0625, 0.075, 0.09) samples showed improved ferroelectric properties and reduced leakage current density in comparison with undoped BiFeO3. Gradual increase in Gd content in BiFeO3 led to enhanced magnetic responses and weak ferromagnetic behavior.",
publisher = "Elsevier Sci Ltd, Oxford",
journal = "Ceramics International",
title = "Change in structural, ferroelectric, and magnetic properties of bismuth ferrite induced by doping with gadolinium",
pages = "19165-19158",
number = "15",
volume = "45",
doi = "10.1016/j.ceramint.2019.06.162"
}

Luković-Golić, D., Radojković, A., Dapčević, A., Pajić, D., Dragović, J., Torić, F., Ćirković, J., Branković, G.,& Branković, Z.. (2019). Change in structural, ferroelectric, and magnetic properties of bismuth ferrite induced by doping with gadolinium. in Ceramics International
Elsevier Sci Ltd, Oxford., 45(15), 19158-19165.
https://doi.org/10.1016/j.ceramint.2019.06.162

Luković-Golić D, Radojković A, Dapčević A, Pajić D, Dragović J, Torić F, Ćirković J, Branković G, Branković Z. Change in structural, ferroelectric, and magnetic properties of bismuth ferrite induced by doping with gadolinium. in Ceramics International. 2019;45(15):19158-19165.
doi:10.1016/j.ceramint.2019.06.162 .

Luković-Golić, Danijela, Radojković, Aleksandar, Dapčević, Aleksandra, Pajić, Damir, Dragović, Jure, Torić, Filip, Ćirković, Jovana, Branković, Goran, Branković, Zorica, "Change in structural, ferroelectric, and magnetic properties of bismuth ferrite induced by doping with gadolinium" in Ceramics International, 45, no. 15 (2019):19158-19165,
https://doi.org/10.1016/j.ceramint.2019.06.162 . .

TY  - JOUR
AU  - Džunuzović, Jasna
AU  - Stefanović, Ivan
AU  - Džunuzović, Enis
AU  - Dapčević, Aleksandra
AU  - Šešlija, Sanja
AU  - Balanč, Bojana
AU  - Lamae, Giuseppe C.
PY  - 2019
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4118
AB  - A series of environmentally friendly polyurethane (PU) networks based on polycaprolactone as soft segment (SS) and Boltorn (R) aliphatic hyperbranched polyester of the second pseudo generation as crosslinking agent was prepared by a two-step polymerization in solution. The chemical structure of the PU networks was analyzed by Fourier transform infrared spectroscopy, while XRD analysis revealed that these samples are amorphous. Swelling measurements, water absorption study, dynamic mechanical analysis, differential scanning calorimetry, thermogravimetric analysis, mechanical tests and scanning electron microscope revealed that, swelling behavior, hydrophobicity, thermal and mechanical features and morphology of PU networks show clear dependence on polycaprolactone content. The increase of the SS content induced appearance of the microphase separated morphology, increase of thermal stability, elongation at break, hydrophobicity and swelling ability in tetrahydrofuran and toluene, but at the same time it is responsible for the decrease of crosslinking density, glass transition temperatures, rigidity, tensile strength and Young's modulus of PU networks. Scanning electron microscope images of the fracture surfaces of PU networks show that their surface is rough, irregular, with flake-like structure, where size of flakes increases with increasing SS content. These results indicate that by choosing adequate SS content, PU coatings with diverse features based on polycaprolactone and Boltorn (R) aliphatic hyperbranched polyester can be designed for appropriate and desired application.
PB  - Elsevier Science Sa, Lausanne
T2  - Progress in Organic Coatings
T1  - Polyurethane networks based on polycaprolactone and hyperbranched polyester: Structural, thermal and mechanical investigation
VL  - 137
DO  - 10.1016/j.porgcoat.2019.105305
ER  - 

@article{
author = "Džunuzović, Jasna and Stefanović, Ivan and Džunuzović, Enis and Dapčević, Aleksandra and Šešlija, Sanja and Balanč, Bojana and Lamae, Giuseppe C.",
year = "2019",
abstract = "A series of environmentally friendly polyurethane (PU) networks based on polycaprolactone as soft segment (SS) and Boltorn (R) aliphatic hyperbranched polyester of the second pseudo generation as crosslinking agent was prepared by a two-step polymerization in solution. The chemical structure of the PU networks was analyzed by Fourier transform infrared spectroscopy, while XRD analysis revealed that these samples are amorphous. Swelling measurements, water absorption study, dynamic mechanical analysis, differential scanning calorimetry, thermogravimetric analysis, mechanical tests and scanning electron microscope revealed that, swelling behavior, hydrophobicity, thermal and mechanical features and morphology of PU networks show clear dependence on polycaprolactone content. The increase of the SS content induced appearance of the microphase separated morphology, increase of thermal stability, elongation at break, hydrophobicity and swelling ability in tetrahydrofuran and toluene, but at the same time it is responsible for the decrease of crosslinking density, glass transition temperatures, rigidity, tensile strength and Young's modulus of PU networks. Scanning electron microscope images of the fracture surfaces of PU networks show that their surface is rough, irregular, with flake-like structure, where size of flakes increases with increasing SS content. These results indicate that by choosing adequate SS content, PU coatings with diverse features based on polycaprolactone and Boltorn (R) aliphatic hyperbranched polyester can be designed for appropriate and desired application.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Progress in Organic Coatings",
title = "Polyurethane networks based on polycaprolactone and hyperbranched polyester: Structural, thermal and mechanical investigation",
volume = "137",
doi = "10.1016/j.porgcoat.2019.105305"
}

Džunuzović, J., Stefanović, I., Džunuzović, E., Dapčević, A., Šešlija, S., Balanč, B.,& Lamae, G. C.. (2019). Polyurethane networks based on polycaprolactone and hyperbranched polyester: Structural, thermal and mechanical investigation. in Progress in Organic Coatings
Elsevier Science Sa, Lausanne., 137.
https://doi.org/10.1016/j.porgcoat.2019.105305

Džunuzović J, Stefanović I, Džunuzović E, Dapčević A, Šešlija S, Balanč B, Lamae GC. Polyurethane networks based on polycaprolactone and hyperbranched polyester: Structural, thermal and mechanical investigation. in Progress in Organic Coatings. 2019;137.
doi:10.1016/j.porgcoat.2019.105305 .

Džunuzović, Jasna, Stefanović, Ivan, Džunuzović, Enis, Dapčević, Aleksandra, Šešlija, Sanja, Balanč, Bojana, Lamae, Giuseppe C., "Polyurethane networks based on polycaprolactone and hyperbranched polyester: Structural, thermal and mechanical investigation" in Progress in Organic Coatings, 137 (2019),
https://doi.org/10.1016/j.porgcoat.2019.105305 . .

TY  - JOUR
AU  - Pocuca-Nesić, Milica
AU  - Marinković-Stanojević, Zorica
AU  - Cotić-Smole, Patricia
AU  - Dapčević, Aleksandra
AU  - Tasić, Nikola
AU  - Branković, Goran
AU  - Branković, Zorica
PY  - 2019
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4138
AB  - Yttrium manganite (YMnO3) is widely investigated multiferroic material with potential use in many technological applications. In this paper, we report on the preparation and characterization of multiferroic hexagonal YMnO3 ceramics obtained by chemical synthesis route. Precursor powders were prepared by the polymerizable complex method from citrate precursors. After calcination at 900 degrees C the powders contained mixture of Y-Mn-O phases which were further sintered at different temperatures. XRD analysis revealed that sintering at 1400 degrees C resulted in the formation of pure hexagonal YMnO3. Density of the obtained ceramics was 96 %TD. The ceramic samples proved to have multiferroic properties - they are antiferromagnetic below 42 K with linear dependence of magnetization as a function of applied magnetic field. The ferroelectric measurements performed at room temperature showed remanent polarization of 0.21 mu C/cm(2) and the coercive field of 6.0 kV/cm for the YMnO3 sample sintered at 1400 degrees C. The magnetization curves measured at 2 and 5 K for the powder samples calcined at 900 degrees C and ceramic samples sintered at 1300 degrees C exhibited a hysteresis loop due to a small concentration of Mn3O4 in the samples.
PB  - Univerzitet u Novom Sadu - Tehnološki fakultet, Novi Sad
T2  - Processing and Application of Ceramics
T1  - Processing and properties of pure antiferromagnetic h-YMnO3
EP  - 434
IS  - 4
SP  - 427
VL  - 13
DO  - 10.2298/PAC1904427P
ER  - 

@article{
author = "Pocuca-Nesić, Milica and Marinković-Stanojević, Zorica and Cotić-Smole, Patricia and Dapčević, Aleksandra and Tasić, Nikola and Branković, Goran and Branković, Zorica",
year = "2019",
abstract = "Yttrium manganite (YMnO3) is widely investigated multiferroic material with potential use in many technological applications. In this paper, we report on the preparation and characterization of multiferroic hexagonal YMnO3 ceramics obtained by chemical synthesis route. Precursor powders were prepared by the polymerizable complex method from citrate precursors. After calcination at 900 degrees C the powders contained mixture of Y-Mn-O phases which were further sintered at different temperatures. XRD analysis revealed that sintering at 1400 degrees C resulted in the formation of pure hexagonal YMnO3. Density of the obtained ceramics was 96 %TD. The ceramic samples proved to have multiferroic properties - they are antiferromagnetic below 42 K with linear dependence of magnetization as a function of applied magnetic field. The ferroelectric measurements performed at room temperature showed remanent polarization of 0.21 mu C/cm(2) and the coercive field of 6.0 kV/cm for the YMnO3 sample sintered at 1400 degrees C. The magnetization curves measured at 2 and 5 K for the powder samples calcined at 900 degrees C and ceramic samples sintered at 1300 degrees C exhibited a hysteresis loop due to a small concentration of Mn3O4 in the samples.",
publisher = "Univerzitet u Novom Sadu - Tehnološki fakultet, Novi Sad",
journal = "Processing and Application of Ceramics",
title = "Processing and properties of pure antiferromagnetic h-YMnO3",
pages = "434-427",
number = "4",
volume = "13",
doi = "10.2298/PAC1904427P"
}

Pocuca-Nesić, M., Marinković-Stanojević, Z., Cotić-Smole, P., Dapčević, A., Tasić, N., Branković, G.,& Branković, Z.. (2019). Processing and properties of pure antiferromagnetic h-YMnO3. in Processing and Application of Ceramics
Univerzitet u Novom Sadu - Tehnološki fakultet, Novi Sad., 13(4), 427-434.
https://doi.org/10.2298/PAC1904427P

Pocuca-Nesić M, Marinković-Stanojević Z, Cotić-Smole P, Dapčević A, Tasić N, Branković G, Branković Z. Processing and properties of pure antiferromagnetic h-YMnO3. in Processing and Application of Ceramics. 2019;13(4):427-434.
doi:10.2298/PAC1904427P .

Pocuca-Nesić, Milica, Marinković-Stanojević, Zorica, Cotić-Smole, Patricia, Dapčević, Aleksandra, Tasić, Nikola, Branković, Goran, Branković, Zorica, "Processing and properties of pure antiferromagnetic h-YMnO3" in Processing and Application of Ceramics, 13, no. 4 (2019):427-434,
https://doi.org/10.2298/PAC1904427P . .

TY  - JOUR
AU  - Marković, Bojana M.
AU  - Spasojević, Vojislav
AU  - Dapčević, Aleksandra
AU  - Vuković, Zorica M.
AU  - Pavlović, Vladimir B.
AU  - Ranđelović, Danijela
AU  - Nastasović, Aleksandra
PY  - 2019
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4179
AB  - Magnetic and non-magnetic macroporous crosslinked copolymers of glycidyl methacrylate and trimethylolpropane trimethacrylate were prepared by suspension copolymerization and functionalized with diethylenetriamine. The samples were characterized by mercury porosimetry, scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDS), Fourier transform infrared spectroscopy analysis (FTIR-ATR), thermogravimetric analysis (TGA), X-ray diffractometry (XRD), atomic force microscopy (AFM), transmission electron microscopy (TEM) and SQUID magnetometry. The FTIR-ATR analysis of synthesized magnetic nanocomposites confirmed the presence of magnetite and successful aminofunctionalization. Non-functionalized and amino-functionalized nanocomposites exhibited superparamagnetic behavior at 300 K, with a saturation magnetization of 5.0 emu/g and 2.9 emu/g, respectively. TEM analysis of the magnetic nanocomposite has shown that magnetic nanoparticles were homogeneously dispersed in the polymer matrix. It was demonstrated that incorporation of magnetic nanoparticles enhanced the thermal stability of the magnetic nanocomposite in comparison to the initial non-magnetic macroporous copolymer.
PB  - Savez hemijskih inženjera, Beograd
T2  - Hemijska industrija
T1  - Characterization of glycidyl methacrylate based magnetic nanocomposites
EP  - 35
IS  - 1
SP  - 25
VL  - 73
DO  - 10.2298/HEMIND181113006M
ER  - 

@article{
author = "Marković, Bojana M. and Spasojević, Vojislav and Dapčević, Aleksandra and Vuković, Zorica M. and Pavlović, Vladimir B. and Ranđelović, Danijela and Nastasović, Aleksandra",
year = "2019",
abstract = "Magnetic and non-magnetic macroporous crosslinked copolymers of glycidyl methacrylate and trimethylolpropane trimethacrylate were prepared by suspension copolymerization and functionalized with diethylenetriamine. The samples were characterized by mercury porosimetry, scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDS), Fourier transform infrared spectroscopy analysis (FTIR-ATR), thermogravimetric analysis (TGA), X-ray diffractometry (XRD), atomic force microscopy (AFM), transmission electron microscopy (TEM) and SQUID magnetometry. The FTIR-ATR analysis of synthesized magnetic nanocomposites confirmed the presence of magnetite and successful aminofunctionalization. Non-functionalized and amino-functionalized nanocomposites exhibited superparamagnetic behavior at 300 K, with a saturation magnetization of 5.0 emu/g and 2.9 emu/g, respectively. TEM analysis of the magnetic nanocomposite has shown that magnetic nanoparticles were homogeneously dispersed in the polymer matrix. It was demonstrated that incorporation of magnetic nanoparticles enhanced the thermal stability of the magnetic nanocomposite in comparison to the initial non-magnetic macroporous copolymer.",
publisher = "Savez hemijskih inženjera, Beograd",
journal = "Hemijska industrija",
title = "Characterization of glycidyl methacrylate based magnetic nanocomposites",
pages = "35-25",
number = "1",
volume = "73",
doi = "10.2298/HEMIND181113006M"
}

Marković, B. M., Spasojević, V., Dapčević, A., Vuković, Z. M., Pavlović, V. B., Ranđelović, D.,& Nastasović, A.. (2019). Characterization of glycidyl methacrylate based magnetic nanocomposites. in Hemijska industrija
Savez hemijskih inženjera, Beograd., 73(1), 25-35.
https://doi.org/10.2298/HEMIND181113006M

Marković BM, Spasojević V, Dapčević A, Vuković ZM, Pavlović VB, Ranđelović D, Nastasović A. Characterization of glycidyl methacrylate based magnetic nanocomposites. in Hemijska industrija. 2019;73(1):25-35.
doi:10.2298/HEMIND181113006M .

Marković, Bojana M., Spasojević, Vojislav, Dapčević, Aleksandra, Vuković, Zorica M., Pavlović, Vladimir B., Ranđelović, Danijela, Nastasović, Aleksandra, "Characterization of glycidyl methacrylate based magnetic nanocomposites" in Hemijska industrija, 73, no. 1 (2019):25-35,
https://doi.org/10.2298/HEMIND181113006M . .

TY  - JOUR
AU  - Obradović, Nina
AU  - Fahrenholtz, William G.
AU  - Filipović, Suzana
AU  - Kosanović, Darko
AU  - Dapčević, Aleksandra
AU  - Đorđević, Antonije
AU  - Balać, Igor
AU  - Pavlović, Vladimir B.
PY  - 2019
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4264
AB  - Magnesium aluminate, MgAl2O4 and other alumina-based spinels are ceramics with high hardness, high melting point and mechanical strenght. Spinels can also be used as dielectrics in microwave applications. The goal of this study was to examine the effects of mechanical activation and sintering temperatures on physico-chemical properties of spinel. MgAl2O4 was produced by solid state reaction between MgO and alpha-Al2O3. The starting powders were mixed by ball milling to homogenize without significant particle size reduction. Mechanical activation of mixed powders was performed in a high-energy planetary ball mill in air for 1 h. Powders were compacted at 300 MPa. Heat treatments were performed in air, at temperatures ranging from 1200 to 1600 degrees C with 2 h dwell time, to determine the amount of spinel formation as a function of temperature. Phase composition and microstructure of initial powders and heated samples were determined by means of X-ray diffraction, particle size analysis, and scanning electron microscopy. The influences of milling and consolidation parameters were studied by electrical measurements and mechanical characterization. The main conclusion of this study was that mechanical activation for 60 min initiated a mechano-chemical reaction, resulted in spinel formation at much lower temperatures than within non-activated powders, and indicated that final sintering stage started at much lower temperatures for activated powders. Changes in microstructure parameters, as a consequence of mechanical treatment and subsequent heating of investigated powder mixtures, strongly affect electrical and mechanical properties of the final ceramics.
PB  - Elsevier Sci Ltd, Oxford
T2  - Ceramics International
T1  - The effect of mechanical activation on synthesis and properties of MgAl2O4 ceramics
EP  - 12021
IS  - 9
SP  - 12015
VL  - 45
DO  - 10.1016/j.ceramint.2019.03.095
ER  - 

@article{
author = "Obradović, Nina and Fahrenholtz, William G. and Filipović, Suzana and Kosanović, Darko and Dapčević, Aleksandra and Đorđević, Antonije and Balać, Igor and Pavlović, Vladimir B.",
year = "2019",
abstract = "Magnesium aluminate, MgAl2O4 and other alumina-based spinels are ceramics with high hardness, high melting point and mechanical strenght. Spinels can also be used as dielectrics in microwave applications. The goal of this study was to examine the effects of mechanical activation and sintering temperatures on physico-chemical properties of spinel. MgAl2O4 was produced by solid state reaction between MgO and alpha-Al2O3. The starting powders were mixed by ball milling to homogenize without significant particle size reduction. Mechanical activation of mixed powders was performed in a high-energy planetary ball mill in air for 1 h. Powders were compacted at 300 MPa. Heat treatments were performed in air, at temperatures ranging from 1200 to 1600 degrees C with 2 h dwell time, to determine the amount of spinel formation as a function of temperature. Phase composition and microstructure of initial powders and heated samples were determined by means of X-ray diffraction, particle size analysis, and scanning electron microscopy. The influences of milling and consolidation parameters were studied by electrical measurements and mechanical characterization. The main conclusion of this study was that mechanical activation for 60 min initiated a mechano-chemical reaction, resulted in spinel formation at much lower temperatures than within non-activated powders, and indicated that final sintering stage started at much lower temperatures for activated powders. Changes in microstructure parameters, as a consequence of mechanical treatment and subsequent heating of investigated powder mixtures, strongly affect electrical and mechanical properties of the final ceramics.",
publisher = "Elsevier Sci Ltd, Oxford",
journal = "Ceramics International",
title = "The effect of mechanical activation on synthesis and properties of MgAl2O4 ceramics",
pages = "12021-12015",
number = "9",
volume = "45",
doi = "10.1016/j.ceramint.2019.03.095"
}

Obradović, N., Fahrenholtz, W. G., Filipović, S., Kosanović, D., Dapčević, A., Đorđević, A., Balać, I.,& Pavlović, V. B.. (2019). The effect of mechanical activation on synthesis and properties of MgAl2O4 ceramics. in Ceramics International
Elsevier Sci Ltd, Oxford., 45(9), 12015-12021.
https://doi.org/10.1016/j.ceramint.2019.03.095

Obradović N, Fahrenholtz WG, Filipović S, Kosanović D, Dapčević A, Đorđević A, Balać I, Pavlović VB. The effect of mechanical activation on synthesis and properties of MgAl2O4 ceramics. in Ceramics International. 2019;45(9):12015-12021.
doi:10.1016/j.ceramint.2019.03.095 .

Obradović, Nina, Fahrenholtz, William G., Filipović, Suzana, Kosanović, Darko, Dapčević, Aleksandra, Đorđević, Antonije, Balać, Igor, Pavlović, Vladimir B., "The effect of mechanical activation on synthesis and properties of MgAl2O4 ceramics" in Ceramics International, 45, no. 9 (2019):12015-12021,
https://doi.org/10.1016/j.ceramint.2019.03.095 . .

TY  - JOUR
AU  - Simović, Bojana
AU  - Dapčević, Aleksandra
AU  - Zdravković, J.
AU  - Tasić, Nikola
AU  - Kovač, S.
AU  - Krstić, Jugoslav
AU  - Branković, Goran
PY  - 2019
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4321
AB  - In this work, nine products were prepared by modifying the experimental conditions (6, 12 and 18 hat 110, 135 and 160 degrees C) of hydrothermal treatment of starting nanoanatase in significantly less concentrated alkaline medium than usual in order to obtain a pure titanate phase. The nanocrystalline samples were characterized by XRPD, FESEM, HRTEM/SAED, EDS, TG, FT-IR, UV-Vis and BET analyses. The results revealed that the structure, texture, morphology and band gap energy of samples strongly depend on conditions of hydrothermal treatment. The intensification of hydrothermal treatment significantly increases the solubility of TiO2 promoting the changes in morphology from nearly spherical titania nanoparticles to elongated titanate nanosheets. The single titanate phase was obtained after energetically the most intensive treatment, i.e. 18 hat 160 degrees C. The step-by-step optimization was thus necessary to finally distinguish the titanates from titania in terms of structural and spectral properties and to finally allow the clarification of long-standing confusion between titania and titanates. The obtained single titanate phase was furtherly used to fabricate a humidity sensor, which showed remarkably rapid response and quick recovery time.
PB  - Elsevier Science Sa, Lausanne
T2  - Journal of Alloys and Compounds
T1  - From titania to titanates: Phase and morphological transition in less alkaline medium under mild conditions
EP  - 819
SP  - 810
VL  - 781
DO  - 10.1016/j.jallcom.2018.12.039
ER  - 

@article{
author = "Simović, Bojana and Dapčević, Aleksandra and Zdravković, J. and Tasić, Nikola and Kovač, S. and Krstić, Jugoslav and Branković, Goran",
year = "2019",
abstract = "In this work, nine products were prepared by modifying the experimental conditions (6, 12 and 18 hat 110, 135 and 160 degrees C) of hydrothermal treatment of starting nanoanatase in significantly less concentrated alkaline medium than usual in order to obtain a pure titanate phase. The nanocrystalline samples were characterized by XRPD, FESEM, HRTEM/SAED, EDS, TG, FT-IR, UV-Vis and BET analyses. The results revealed that the structure, texture, morphology and band gap energy of samples strongly depend on conditions of hydrothermal treatment. The intensification of hydrothermal treatment significantly increases the solubility of TiO2 promoting the changes in morphology from nearly spherical titania nanoparticles to elongated titanate nanosheets. The single titanate phase was obtained after energetically the most intensive treatment, i.e. 18 hat 160 degrees C. The step-by-step optimization was thus necessary to finally distinguish the titanates from titania in terms of structural and spectral properties and to finally allow the clarification of long-standing confusion between titania and titanates. The obtained single titanate phase was furtherly used to fabricate a humidity sensor, which showed remarkably rapid response and quick recovery time.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Journal of Alloys and Compounds",
title = "From titania to titanates: Phase and morphological transition in less alkaline medium under mild conditions",
pages = "819-810",
volume = "781",
doi = "10.1016/j.jallcom.2018.12.039"
}

Simović, B., Dapčević, A., Zdravković, J., Tasić, N., Kovač, S., Krstić, J.,& Branković, G.. (2019). From titania to titanates: Phase and morphological transition in less alkaline medium under mild conditions. in Journal of Alloys and Compounds
Elsevier Science Sa, Lausanne., 781, 810-819.
https://doi.org/10.1016/j.jallcom.2018.12.039

Simović B, Dapčević A, Zdravković J, Tasić N, Kovač S, Krstić J, Branković G. From titania to titanates: Phase and morphological transition in less alkaline medium under mild conditions. in Journal of Alloys and Compounds. 2019;781:810-819.
doi:10.1016/j.jallcom.2018.12.039 .

Simović, Bojana, Dapčević, Aleksandra, Zdravković, J., Tasić, Nikola, Kovač, S., Krstić, Jugoslav, Branković, Goran, "From titania to titanates: Phase and morphological transition in less alkaline medium under mild conditions" in Journal of Alloys and Compounds, 781 (2019):810-819,
https://doi.org/10.1016/j.jallcom.2018.12.039 . .

TY  - JOUR
AU  - Đuriš, Jelena
AU  - Milovanović, Stoja
AU  - Medarević, Đorđe
AU  - Dobričić, Vladimir
AU  - Dapčević, Aleksandra
AU  - Ibrić, Svetlana
PY  - 2019
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4335
AB  - Solid dispersions production is one of the substantial approaches for improvement of poor drug solubility. Additionally, supercritical fluid assisted method for preparation of solid dispersions can offer many advantages in comparison to the conventional melting or solvent-evaporation methods. Miscibility analysis provides valuable guidance for selection of the most appropriate polymeric carrier for dispersion of the drug of interest. In addition to the increased drug release rate, solid dispersions should have proper mechanical attributes in order to be successfully formulated in the final solid dosage form such as tablet. Therefore, several pharmaceutical grade polymers have been selected for development of BCS Class II drug carvedilol (CARV) solid dispersions. They were compared based on behavior in supercritical CO2 and affinity towards CARV calculated from the miscibility analysis. By utilization of the supercritical CO2 assisted method, solid dispersions of CARV with the selected (co) polymers (polyvinylpyrrolidone (PVP), hydroxypropyl methylcellulose (HPMC), Soluplus (R) and Eudragit (R)) were obtained. Properties of the prepared CARV-polymer dispersions were observed by the polarizing and scanning electron microscopy and analyzed by differential scanning calorimetry and Fourier transform infrared spectroscopy. CARV was additionally characterized by X-ray powder diffraction. Furthermore, in vitro dissolution studies and dynamic compaction analysis were performed on the selected samples of solid dispersions. Among the studied polymers, PVP and HPMC have been identified as polymers with the highest affinity towards CARV, based on the calculated delta(p) values. This has been also confirmed with the highest dissolution efficiency of CARV-PVP and CARV-HPMC solid dispersions. Solid state characterization indicated that CARV was dispersed either molecularly, or in the amorphous form, depending on interactions with each polymer. Determination of CARV-PVP and CARV-HPMC mechanical properties revealed that CARV-PVP solid dispersion has superior compactibility and tabletability. Therefore, CARV-PVP solid dispersion has been highlighted as the most appropriate for the further development of tablets as the final dosage form. Presented study provides an example for efficient approach for development of poorly soluble drug solid dispersion with satisfactory tableting properties.
PB  - Elsevier Science Bv, Amsterdam
T2  - International Journal of Pharmaceutics
T1  - Selection of the suitable polymer for supercritical fluid assisted preparation of carvedilol solid dispersions
EP  - 200
SP  - 190
VL  - 554
DO  - 10.1016/j.ijpharm.2018.11.015
ER  - 

@article{
author = "Đuriš, Jelena and Milovanović, Stoja and Medarević, Đorđe and Dobričić, Vladimir and Dapčević, Aleksandra and Ibrić, Svetlana",
year = "2019",
abstract = "Solid dispersions production is one of the substantial approaches for improvement of poor drug solubility. Additionally, supercritical fluid assisted method for preparation of solid dispersions can offer many advantages in comparison to the conventional melting or solvent-evaporation methods. Miscibility analysis provides valuable guidance for selection of the most appropriate polymeric carrier for dispersion of the drug of interest. In addition to the increased drug release rate, solid dispersions should have proper mechanical attributes in order to be successfully formulated in the final solid dosage form such as tablet. Therefore, several pharmaceutical grade polymers have been selected for development of BCS Class II drug carvedilol (CARV) solid dispersions. They were compared based on behavior in supercritical CO2 and affinity towards CARV calculated from the miscibility analysis. By utilization of the supercritical CO2 assisted method, solid dispersions of CARV with the selected (co) polymers (polyvinylpyrrolidone (PVP), hydroxypropyl methylcellulose (HPMC), Soluplus (R) and Eudragit (R)) were obtained. Properties of the prepared CARV-polymer dispersions were observed by the polarizing and scanning electron microscopy and analyzed by differential scanning calorimetry and Fourier transform infrared spectroscopy. CARV was additionally characterized by X-ray powder diffraction. Furthermore, in vitro dissolution studies and dynamic compaction analysis were performed on the selected samples of solid dispersions. Among the studied polymers, PVP and HPMC have been identified as polymers with the highest affinity towards CARV, based on the calculated delta(p) values. This has been also confirmed with the highest dissolution efficiency of CARV-PVP and CARV-HPMC solid dispersions. Solid state characterization indicated that CARV was dispersed either molecularly, or in the amorphous form, depending on interactions with each polymer. Determination of CARV-PVP and CARV-HPMC mechanical properties revealed that CARV-PVP solid dispersion has superior compactibility and tabletability. Therefore, CARV-PVP solid dispersion has been highlighted as the most appropriate for the further development of tablets as the final dosage form. Presented study provides an example for efficient approach for development of poorly soluble drug solid dispersion with satisfactory tableting properties.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "International Journal of Pharmaceutics",
title = "Selection of the suitable polymer for supercritical fluid assisted preparation of carvedilol solid dispersions",
pages = "200-190",
volume = "554",
doi = "10.1016/j.ijpharm.2018.11.015"
}

Đuriš, J., Milovanović, S., Medarević, Đ., Dobričić, V., Dapčević, A.,& Ibrić, S.. (2019). Selection of the suitable polymer for supercritical fluid assisted preparation of carvedilol solid dispersions. in International Journal of Pharmaceutics
Elsevier Science Bv, Amsterdam., 554, 190-200.
https://doi.org/10.1016/j.ijpharm.2018.11.015

Đuriš J, Milovanović S, Medarević Đ, Dobričić V, Dapčević A, Ibrić S. Selection of the suitable polymer for supercritical fluid assisted preparation of carvedilol solid dispersions. in International Journal of Pharmaceutics. 2019;554:190-200.
doi:10.1016/j.ijpharm.2018.11.015 .

Đuriš, Jelena, Milovanović, Stoja, Medarević, Đorđe, Dobričić, Vladimir, Dapčević, Aleksandra, Ibrić, Svetlana, "Selection of the suitable polymer for supercritical fluid assisted preparation of carvedilol solid dispersions" in International Journal of Pharmaceutics, 554 (2019):190-200,
https://doi.org/10.1016/j.ijpharm.2018.11.015 . .

TY  - JOUR
AU  - Djuris, Jelena
AU  - Milovanovic, Stoja
AU  - Medarevic, Djordje
AU  - Dobricic, Vladimir
AU  - Dapčević, Aleksandra
AU  - Ibric, Svetlana
PY  - 2019
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5030
AB  - Solid dispersions production is one of the substantial approaches for improvement of poor drug solubility. Additionally, supercritical fluid assisted method for preparation of solid dispersions can offer many advantages in comparison to the conventional melting or solvent-evaporation methods. Miscibility analysis provides valuable guidance for selection of the most appropriate polymeric carrier for dispersion of the drug of interest. In addition to the increased drug release rate, solid dispersions should have proper mechanical attributes in order to be successfully formulated in the final solid dosage form such as tablet. Therefore, several pharmaceutical grade polymers have been selected for development of BCS Class II drug carvedilol (CARV) solid dispersions. They were compared based on behavior in supercritical CO 2 and affinity towards CARV calculated from the miscibility analysis. By utilization of the supercritical CO 2 assisted method, solid dispersions of CARV with the selected (co)polymers (polyvinylpyrrolidone (PVP), hydroxypropyl methylcellulose (HPMC), Soluplus® and Eudragit®) were obtained. Properties of the prepared CARV-polymer dispersions were observed by the polarizing and scanning electron microscopy and analyzed by differential scanning calorimetry and Fourier transform infrared spectroscopy. CARV was additionally characterized by X-ray powder diffraction. Furthermore, in vitro dissolution studies and dynamic compaction analysis were performed on the selected samples of solid dispersions. Among the studied polymers, PVP and HPMC have been identified as polymers with the highest affinity towards CARV, based on the calculated δ p values. This has been also confirmed with the highest dissolution efficiency of CARV-PVP and CARV-HPMC solid dispersions. Solid state characterization indicated that CARV was dispersed either molecularly, or in the amorphous form, depending on interactions with each polymer. Determination of CARV-PVP and CARV-HPMC mechanical properties revealed that CARV-PVP solid dispersion has superior compactibility and tabletability. Therefore, CARV-PVP solid dispersion has been highlighted as the most appropriate for the further development of tablets as the final dosage form. Presented study provides an example for efficient approach for development of poorly soluble drug solid dispersion with satisfactory tableting properties.
PB  - Elsevier B.V.
T2  - International Journal of Pharmaceutics
T1  - Selection of the suitable polymer for supercritical fluid assisted preparation of carvedilol  solid dispersions
EP  - 200
SP  - 190
VL  - 554
DO  - 10.1016/j.ijpharm.2018.11.015
ER  - 

@article{
author = "Djuris, Jelena and Milovanovic, Stoja and Medarevic, Djordje and Dobricic, Vladimir and Dapčević, Aleksandra and Ibric, Svetlana",
year = "2019",
abstract = "Solid dispersions production is one of the substantial approaches for improvement of poor drug solubility. Additionally, supercritical fluid assisted method for preparation of solid dispersions can offer many advantages in comparison to the conventional melting or solvent-evaporation methods. Miscibility analysis provides valuable guidance for selection of the most appropriate polymeric carrier for dispersion of the drug of interest. In addition to the increased drug release rate, solid dispersions should have proper mechanical attributes in order to be successfully formulated in the final solid dosage form such as tablet. Therefore, several pharmaceutical grade polymers have been selected for development of BCS Class II drug carvedilol (CARV) solid dispersions. They were compared based on behavior in supercritical CO 2 and affinity towards CARV calculated from the miscibility analysis. By utilization of the supercritical CO 2 assisted method, solid dispersions of CARV with the selected (co)polymers (polyvinylpyrrolidone (PVP), hydroxypropyl methylcellulose (HPMC), Soluplus® and Eudragit®) were obtained. Properties of the prepared CARV-polymer dispersions were observed by the polarizing and scanning electron microscopy and analyzed by differential scanning calorimetry and Fourier transform infrared spectroscopy. CARV was additionally characterized by X-ray powder diffraction. Furthermore, in vitro dissolution studies and dynamic compaction analysis were performed on the selected samples of solid dispersions. Among the studied polymers, PVP and HPMC have been identified as polymers with the highest affinity towards CARV, based on the calculated δ p values. This has been also confirmed with the highest dissolution efficiency of CARV-PVP and CARV-HPMC solid dispersions. Solid state characterization indicated that CARV was dispersed either molecularly, or in the amorphous form, depending on interactions with each polymer. Determination of CARV-PVP and CARV-HPMC mechanical properties revealed that CARV-PVP solid dispersion has superior compactibility and tabletability. Therefore, CARV-PVP solid dispersion has been highlighted as the most appropriate for the further development of tablets as the final dosage form. Presented study provides an example for efficient approach for development of poorly soluble drug solid dispersion with satisfactory tableting properties.",
publisher = "Elsevier B.V.",
journal = "International Journal of Pharmaceutics",
title = "Selection of the suitable polymer for supercritical fluid assisted preparation of carvedilol  solid dispersions",
pages = "200-190",
volume = "554",
doi = "10.1016/j.ijpharm.2018.11.015"
}

Djuris, J., Milovanovic, S., Medarevic, D., Dobricic, V., Dapčević, A.,& Ibric, S.. (2019). Selection of the suitable polymer for supercritical fluid assisted preparation of carvedilol  solid dispersions. in International Journal of Pharmaceutics
Elsevier B.V.., 554, 190-200.
https://doi.org/10.1016/j.ijpharm.2018.11.015

Djuris J, Milovanovic S, Medarevic D, Dobricic V, Dapčević A, Ibric S. Selection of the suitable polymer for supercritical fluid assisted preparation of carvedilol  solid dispersions. in International Journal of Pharmaceutics. 2019;554:190-200.
doi:10.1016/j.ijpharm.2018.11.015 .

Djuris, Jelena, Milovanovic, Stoja, Medarevic, Djordje, Dobricic, Vladimir, Dapčević, Aleksandra, Ibric, Svetlana, "Selection of the suitable polymer for supercritical fluid assisted preparation of carvedilol  solid dispersions" in International Journal of Pharmaceutics, 554 (2019):190-200,
https://doi.org/10.1016/j.ijpharm.2018.11.015 . .

TY  - JOUR
AU  - Matović, Luka
AU  - Tasić, Nikola
AU  - Trišović, Nemanja
AU  - Lađarević, Jelena
AU  - Vitnik, Vesna
AU  - Vitnik, Željko
AU  - Grgur, Branimir
AU  - Mijin, Dušan
PY  - 2019
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4073
AB  - In order to get a better insight into the relationship between molecular structure and photovoltaic performance, six monoazo dye molecules containing benzoic and cinnamic acid moieties were synthesized and their photovoltaic properties were studied. Three of them have not been previously used in solar cells. Spectroscopic measurements of the investigated compounds coupled with theoretical calculations were performed. Short-circuit current density, open-circuit voltage, and fill-factor were determined. It was found that a larger amount of short-circuit current density will be generated if the HOMO-LUMO energy gap is lower, determined by the stability of the molecule and the electronic effect of the donor moiety. Among both series of synthesized dye molecules, the highest obtained values of short-circuit current density were achieved with (2-hydroxynaphthalene-1-ylazo)benzoic acid and (2-hydroxynaphthalene-1-ylazo)cinnamic acid, and thus they were regarded as promising candidates for application in dye-sensitized solar cells.
PB  - Scientific Technical Research Council Turkey-Tubitak, Ankara
T2  - Turkish Journal of Chemistry
T1  - On the azo dyes derived from benzoic and cinnamic acids used as photosensitizers in dye-sensitized solar cells
EP  - 1203
IS  - 4
SP  - 1183
VL  - 43
DO  - 10.3906/kim-1903-76
ER  - 

@article{
author = "Matović, Luka and Tasić, Nikola and Trišović, Nemanja and Lađarević, Jelena and Vitnik, Vesna and Vitnik, Željko and Grgur, Branimir and Mijin, Dušan",
year = "2019",
abstract = "In order to get a better insight into the relationship between molecular structure and photovoltaic performance, six monoazo dye molecules containing benzoic and cinnamic acid moieties were synthesized and their photovoltaic properties were studied. Three of them have not been previously used in solar cells. Spectroscopic measurements of the investigated compounds coupled with theoretical calculations were performed. Short-circuit current density, open-circuit voltage, and fill-factor were determined. It was found that a larger amount of short-circuit current density will be generated if the HOMO-LUMO energy gap is lower, determined by the stability of the molecule and the electronic effect of the donor moiety. Among both series of synthesized dye molecules, the highest obtained values of short-circuit current density were achieved with (2-hydroxynaphthalene-1-ylazo)benzoic acid and (2-hydroxynaphthalene-1-ylazo)cinnamic acid, and thus they were regarded as promising candidates for application in dye-sensitized solar cells.",
publisher = "Scientific Technical Research Council Turkey-Tubitak, Ankara",
journal = "Turkish Journal of Chemistry",
title = "On the azo dyes derived from benzoic and cinnamic acids used as photosensitizers in dye-sensitized solar cells",
pages = "1203-1183",
number = "4",
volume = "43",
doi = "10.3906/kim-1903-76"
}

Matović, L., Tasić, N., Trišović, N., Lađarević, J., Vitnik, V., Vitnik, Ž., Grgur, B.,& Mijin, D.. (2019). On the azo dyes derived from benzoic and cinnamic acids used as photosensitizers in dye-sensitized solar cells. in Turkish Journal of Chemistry
Scientific Technical Research Council Turkey-Tubitak, Ankara., 43(4), 1183-1203.
https://doi.org/10.3906/kim-1903-76

Matović L, Tasić N, Trišović N, Lađarević J, Vitnik V, Vitnik Ž, Grgur B, Mijin D. On the azo dyes derived from benzoic and cinnamic acids used as photosensitizers in dye-sensitized solar cells. in Turkish Journal of Chemistry. 2019;43(4):1183-1203.
doi:10.3906/kim-1903-76 .

Matović, Luka, Tasić, Nikola, Trišović, Nemanja, Lađarević, Jelena, Vitnik, Vesna, Vitnik, Željko, Grgur, Branimir, Mijin, Dušan, "On the azo dyes derived from benzoic and cinnamic acids used as photosensitizers in dye-sensitized solar cells" in Turkish Journal of Chemistry, 43, no. 4 (2019):1183-1203,
https://doi.org/10.3906/kim-1903-76 . .

TY  - JOUR
AU  - Radović, Marko N.
AU  - Adamović, Tijana
AU  - Pavlović, Jelena
AU  - Rusmirović, Jelena
AU  - Tadić, Vanja
AU  - Branković, Zorica
AU  - Ivanović, Jasna
PY  - 2019
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4232
AB  - Supercritical CO2 impregnation process was used for the first time to fabricate biodegradable gelatin-chitosan (G/Ch) films containing dove oil (CO) for potential use in active food packaging. All the impregnations were carried out at moderately low temperature (40 degrees C). Aiming to maximize CO loading in the films with acceptable morphological, structural and thermal properties, CO2 pressure, impregnation time and G:Ch mass ratio were varied. Gelatin fraction in the films of 25-50 wt. %, scCO(2) pressures of 10-20 MPa and impregnation time of 2-6 h impregnation favoured the CO loading. Processing of the film with equal gelatin to chitosan mass ratio (G/Ch(50:50)) at 10 MPa for 2 h yielded sufficiently high loading (56 mg CO/g(film)) without an adverse effect on morphological properties. The G/Ch(50:50) film was therefore chosen for structural and thermal analyses. ATR-FTIR analysis confirmed successful CO incorporation into the G/Ch(50:50) and its interaction with the film. Plasticizing effect of scCO(2) and CO on the film was evidenced by DSC. Incorporation of 56 mg CO/g(film) into the G/Ch(50:50) didn't affect thermal stability of the film. Beside environmental benefits, supercritical impregnation process enables fast fabrication of G/Ch bio-composite films containing CO, thermally stable to 110 degrees C, which is suitable for most of food packaging applications.
PB  - Savez hemijskih inženjera, Beograd
T2  - Chemical Industry & Chemical Engineering Quarterly
T1  - Supercritical co2 impregnation of gelatin-chitosan films with clove essential oil and characterization thereof
EP  - 130
IS  - 2
SP  - 119
VL  - 25
DO  - 10.2298/CICEQ180323025R
ER  - 

@article{
author = "Radović, Marko N. and Adamović, Tijana and Pavlović, Jelena and Rusmirović, Jelena and Tadić, Vanja and Branković, Zorica and Ivanović, Jasna",
year = "2019",
abstract = "Supercritical CO2 impregnation process was used for the first time to fabricate biodegradable gelatin-chitosan (G/Ch) films containing dove oil (CO) for potential use in active food packaging. All the impregnations were carried out at moderately low temperature (40 degrees C). Aiming to maximize CO loading in the films with acceptable morphological, structural and thermal properties, CO2 pressure, impregnation time and G:Ch mass ratio were varied. Gelatin fraction in the films of 25-50 wt. %, scCO(2) pressures of 10-20 MPa and impregnation time of 2-6 h impregnation favoured the CO loading. Processing of the film with equal gelatin to chitosan mass ratio (G/Ch(50:50)) at 10 MPa for 2 h yielded sufficiently high loading (56 mg CO/g(film)) without an adverse effect on morphological properties. The G/Ch(50:50) film was therefore chosen for structural and thermal analyses. ATR-FTIR analysis confirmed successful CO incorporation into the G/Ch(50:50) and its interaction with the film. Plasticizing effect of scCO(2) and CO on the film was evidenced by DSC. Incorporation of 56 mg CO/g(film) into the G/Ch(50:50) didn't affect thermal stability of the film. Beside environmental benefits, supercritical impregnation process enables fast fabrication of G/Ch bio-composite films containing CO, thermally stable to 110 degrees C, which is suitable for most of food packaging applications.",
publisher = "Savez hemijskih inženjera, Beograd",
journal = "Chemical Industry & Chemical Engineering Quarterly",
title = "Supercritical co2 impregnation of gelatin-chitosan films with clove essential oil and characterization thereof",
pages = "130-119",
number = "2",
volume = "25",
doi = "10.2298/CICEQ180323025R"
}

Radović, M. N., Adamović, T., Pavlović, J., Rusmirović, J., Tadić, V., Branković, Z.,& Ivanović, J.. (2019). Supercritical co2 impregnation of gelatin-chitosan films with clove essential oil and characterization thereof. in Chemical Industry & Chemical Engineering Quarterly
Savez hemijskih inženjera, Beograd., 25(2), 119-130.
https://doi.org/10.2298/CICEQ180323025R

Radović MN, Adamović T, Pavlović J, Rusmirović J, Tadić V, Branković Z, Ivanović J. Supercritical co2 impregnation of gelatin-chitosan films with clove essential oil and characterization thereof. in Chemical Industry & Chemical Engineering Quarterly. 2019;25(2):119-130.
doi:10.2298/CICEQ180323025R .

Radović, Marko N., Adamović, Tijana, Pavlović, Jelena, Rusmirović, Jelena, Tadić, Vanja, Branković, Zorica, Ivanović, Jasna, "Supercritical co2 impregnation of gelatin-chitosan films with clove essential oil and characterization thereof" in Chemical Industry & Chemical Engineering Quarterly, 25, no. 2 (2019):119-130,
https://doi.org/10.2298/CICEQ180323025R . .

TY  - JOUR
AU  - Trišović, Nemanja
AU  - Radovanović, Lidija
AU  - Janjić, Goran V.
AU  - Jelić, Stefan T.
AU  - Rogan, Jelena
PY  - 2019
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4244
AB  - A series of five derivatives of the anticonvulsant drug phenytoin was synthesized, and their crystal structures were determined. The relationship between the molecular and crystal structure of the investigated compounds was rationalized in the context of contribution of intermolecular interactions and supramolecular structural motifs. The conformational preferences were analyzed by comparing the rotational freedom of the phenyl groups in the investigated compounds with 5,5-diphenylhydantoins from the Cambridge Structural Database. With the exception of compound 3 bearing the cyclopropyl group, the crystal packing of the investigated compounds contains centrosymmetric dimers linked by paired N-H center dot center dot center dot O hydrogen bonds, which further self-organize through pairs of C-H center dot center dot center dot O interactions and a parallel interaction of two phenyl rings at a large offset into chains running along the c-axis. The principal feature of the crystal structure of compound 3 is formation of the chains by N-H center dot center dot center dot O hydrogen bonds and C-H center dot center dot center dot O and C-H center dot center dot center dot pi interactions. The coordination of phenytoin enables more rotational freedom for the phenyl groups. An emphasis was placed on docking of the investigated compounds into the voltage-gated ion channel in the open and closed state. The obtained results indicate that hydrogen bonding and hydrophobic interactions are dominant in stabilizing energetically favored orientations of the investigated compounds bound to the protein.
PB  - American Chemical Society (ACS)
T2  - Crystal Growth & Design
T1  - Substituent Effects on the Patterns of Intermolecular Interactions of 3-Alkyl and 3-Cycloalkyl Derivatives of Phenytoin: A Crystallographic and Quantum-Chemical Study
EP  - 2174
IS  - 4
SP  - 2163
VL  - 19
DO  - 10.1021/acs.cgd.8b01776
ER  - 

@article{
author = "Trišović, Nemanja and Radovanović, Lidija and Janjić, Goran V. and Jelić, Stefan T. and Rogan, Jelena",
year = "2019",
abstract = "A series of five derivatives of the anticonvulsant drug phenytoin was synthesized, and their crystal structures were determined. The relationship between the molecular and crystal structure of the investigated compounds was rationalized in the context of contribution of intermolecular interactions and supramolecular structural motifs. The conformational preferences were analyzed by comparing the rotational freedom of the phenyl groups in the investigated compounds with 5,5-diphenylhydantoins from the Cambridge Structural Database. With the exception of compound 3 bearing the cyclopropyl group, the crystal packing of the investigated compounds contains centrosymmetric dimers linked by paired N-H center dot center dot center dot O hydrogen bonds, which further self-organize through pairs of C-H center dot center dot center dot O interactions and a parallel interaction of two phenyl rings at a large offset into chains running along the c-axis. The principal feature of the crystal structure of compound 3 is formation of the chains by N-H center dot center dot center dot O hydrogen bonds and C-H center dot center dot center dot O and C-H center dot center dot center dot pi interactions. The coordination of phenytoin enables more rotational freedom for the phenyl groups. An emphasis was placed on docking of the investigated compounds into the voltage-gated ion channel in the open and closed state. The obtained results indicate that hydrogen bonding and hydrophobic interactions are dominant in stabilizing energetically favored orientations of the investigated compounds bound to the protein.",
publisher = "American Chemical Society (ACS)",
journal = "Crystal Growth & Design",
title = "Substituent Effects on the Patterns of Intermolecular Interactions of 3-Alkyl and 3-Cycloalkyl Derivatives of Phenytoin: A Crystallographic and Quantum-Chemical Study",
pages = "2174-2163",
number = "4",
volume = "19",
doi = "10.1021/acs.cgd.8b01776"
}

Trišović, N., Radovanović, L., Janjić, G. V., Jelić, S. T.,& Rogan, J.. (2019). Substituent Effects on the Patterns of Intermolecular Interactions of 3-Alkyl and 3-Cycloalkyl Derivatives of Phenytoin: A Crystallographic and Quantum-Chemical Study. in Crystal Growth & Design
American Chemical Society (ACS)., 19(4), 2163-2174.
https://doi.org/10.1021/acs.cgd.8b01776

Trišović N, Radovanović L, Janjić GV, Jelić ST, Rogan J. Substituent Effects on the Patterns of Intermolecular Interactions of 3-Alkyl and 3-Cycloalkyl Derivatives of Phenytoin: A Crystallographic and Quantum-Chemical Study. in Crystal Growth & Design. 2019;19(4):2163-2174.
doi:10.1021/acs.cgd.8b01776 .

Trišović, Nemanja, Radovanović, Lidija, Janjić, Goran V., Jelić, Stefan T., Rogan, Jelena, "Substituent Effects on the Patterns of Intermolecular Interactions of 3-Alkyl and 3-Cycloalkyl Derivatives of Phenytoin: A Crystallographic and Quantum-Chemical Study" in Crystal Growth & Design, 19, no. 4 (2019):2163-2174,
https://doi.org/10.1021/acs.cgd.8b01776 . .

TY  - JOUR
AU  - Obradović, Nina
AU  - Fahrenholtz, William G.
AU  - Filipović, Suzana
AU  - Corlett, Cole
AU  - Đorđević, Pavle
AU  - Rogan, Jelena
AU  - Vulić, Predrag
AU  - Buljak, Vladimir
AU  - Pavlović, Vladimir B.
PY  - 2019
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4136
AB  - Single phase MgAl2O4 was made from a one-to-one molar ratio of MgO and Al2O3 powders mixed using ball-milling. Mixtures of MgO and Al2O3 were subsequently treated in planetary ball mill for 30, 60, 90 and 120 minutes in air. The aim of this study was to examine phase composition, microstructure, and densification behavior of sintered specimens. After sintering in dilatometer at 1500 degrees C, the powder was converted to single phase MgAl2O4. The results show that mechanical activation improved the densification behavior of MgAl2O4 sintered specimens, and it reduced the onset temperature for sintering by approx. 100 degrees C. Based on dilatometer data, powders were subsequently densified at 1450 degrees C by hot pressing. Almost all specimens exhibited full density, while sample activated for 30 minutes showed the fastest densification rate.
PB  - Međunarodni Institut za nauku o sinterovanju, Beograd
T2  - Science of Sintering
T1  - Characterization of MgAl2O4 Sintered Ceramics
EP  - 376
IS  - 4
SP  - 363
VL  - 51
DO  - 10.2298/SOS1904363O
ER  - 

@article{
author = "Obradović, Nina and Fahrenholtz, William G. and Filipović, Suzana and Corlett, Cole and Đorđević, Pavle and Rogan, Jelena and Vulić, Predrag and Buljak, Vladimir and Pavlović, Vladimir B.",
year = "2019",
abstract = "Single phase MgAl2O4 was made from a one-to-one molar ratio of MgO and Al2O3 powders mixed using ball-milling. Mixtures of MgO and Al2O3 were subsequently treated in planetary ball mill for 30, 60, 90 and 120 minutes in air. The aim of this study was to examine phase composition, microstructure, and densification behavior of sintered specimens. After sintering in dilatometer at 1500 degrees C, the powder was converted to single phase MgAl2O4. The results show that mechanical activation improved the densification behavior of MgAl2O4 sintered specimens, and it reduced the onset temperature for sintering by approx. 100 degrees C. Based on dilatometer data, powders were subsequently densified at 1450 degrees C by hot pressing. Almost all specimens exhibited full density, while sample activated for 30 minutes showed the fastest densification rate.",
publisher = "Međunarodni Institut za nauku o sinterovanju, Beograd",
journal = "Science of Sintering",
title = "Characterization of MgAl2O4 Sintered Ceramics",
pages = "376-363",
number = "4",
volume = "51",
doi = "10.2298/SOS1904363O"
}

Obradović, N., Fahrenholtz, W. G., Filipović, S., Corlett, C., Đorđević, P., Rogan, J., Vulić, P., Buljak, V.,& Pavlović, V. B.. (2019). Characterization of MgAl2O4 Sintered Ceramics. in Science of Sintering
Međunarodni Institut za nauku o sinterovanju, Beograd., 51(4), 363-376.
https://doi.org/10.2298/SOS1904363O

Obradović N, Fahrenholtz WG, Filipović S, Corlett C, Đorđević P, Rogan J, Vulić P, Buljak V, Pavlović VB. Characterization of MgAl2O4 Sintered Ceramics. in Science of Sintering. 2019;51(4):363-376.
doi:10.2298/SOS1904363O .

Obradović, Nina, Fahrenholtz, William G., Filipović, Suzana, Corlett, Cole, Đorđević, Pavle, Rogan, Jelena, Vulić, Predrag, Buljak, Vladimir, Pavlović, Vladimir B., "Characterization of MgAl2O4 Sintered Ceramics" in Science of Sintering, 51, no. 4 (2019):363-376,
https://doi.org/10.2298/SOS1904363O . .

TY  - JOUR
AU  - Mićović, Dragana
AU  - Pagnacco, Maja C.
AU  - Banković, Predrag
AU  - Maletaškić, Jelena
AU  - Matović, Branko
AU  - Đokić, Veljko
AU  - Stojmenović, Marija
PY  - 2019
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4060
AB  - Potential non-toxic pink and red ceramic pigments based on CeO2 were successfully synthesized by self-propagating room temperature method and thermally treated at 600, 900 and 1200 degrees C for 15 min. The structure, morphology and optical properties, as well as thermal stability of Ce1-xErxO2-delta and Ce1-xPrxO2-delta (x = 0.05) were examined. Single-phase composition of all obtained CeO2 pigments was confirmed using XRPD method and Raman spectroscopy and it was not dependent on temperature. The mechanism of structural behaviour was thoroughly examined using Raman and FTIR spectroscopy. Nanometric dimensions of the crystallites of all pigments were confirmed using XRPD, TEM and FE-SEM analysis. Colour properties were dependent on the temperature treatment, and their position in the chromaticity diagram was studied using UV/VIS spectrophotometry. Colour efficiency measurements were supplemented by colorimetric analysis. It is proved that all samples are thermally stable in the investigated temperature range (up to 1200 degrees C), and their potential application as environmentally friendly pigments of desired colour is confirmed.
PB  - Univerzitet u Novom Sadu - Tehnološki fakultet, Novi Sad
T2  - Processing and Application of Ceramics
T1  - The influence of short thermal treatment on structure, morphology and optical properties of Er and Pr doped ceria pigments: Comparative study
EP  - 321
IS  - 3
SP  - 310
VL  - 13
DO  - 10.2298/PAC1903310M
ER  - 

@article{
author = "Mićović, Dragana and Pagnacco, Maja C. and Banković, Predrag and Maletaškić, Jelena and Matović, Branko and Đokić, Veljko and Stojmenović, Marija",
year = "2019",
abstract = "Potential non-toxic pink and red ceramic pigments based on CeO2 were successfully synthesized by self-propagating room temperature method and thermally treated at 600, 900 and 1200 degrees C for 15 min. The structure, morphology and optical properties, as well as thermal stability of Ce1-xErxO2-delta and Ce1-xPrxO2-delta (x = 0.05) were examined. Single-phase composition of all obtained CeO2 pigments was confirmed using XRPD method and Raman spectroscopy and it was not dependent on temperature. The mechanism of structural behaviour was thoroughly examined using Raman and FTIR spectroscopy. Nanometric dimensions of the crystallites of all pigments were confirmed using XRPD, TEM and FE-SEM analysis. Colour properties were dependent on the temperature treatment, and their position in the chromaticity diagram was studied using UV/VIS spectrophotometry. Colour efficiency measurements were supplemented by colorimetric analysis. It is proved that all samples are thermally stable in the investigated temperature range (up to 1200 degrees C), and their potential application as environmentally friendly pigments of desired colour is confirmed.",
publisher = "Univerzitet u Novom Sadu - Tehnološki fakultet, Novi Sad",
journal = "Processing and Application of Ceramics",
title = "The influence of short thermal treatment on structure, morphology and optical properties of Er and Pr doped ceria pigments: Comparative study",
pages = "321-310",
number = "3",
volume = "13",
doi = "10.2298/PAC1903310M"
}

Mićović, D., Pagnacco, M. C., Banković, P., Maletaškić, J., Matović, B., Đokić, V.,& Stojmenović, M.. (2019). The influence of short thermal treatment on structure, morphology and optical properties of Er and Pr doped ceria pigments: Comparative study. in Processing and Application of Ceramics
Univerzitet u Novom Sadu - Tehnološki fakultet, Novi Sad., 13(3), 310-321.
https://doi.org/10.2298/PAC1903310M

Mićović D, Pagnacco MC, Banković P, Maletaškić J, Matović B, Đokić V, Stojmenović M. The influence of short thermal treatment on structure, morphology and optical properties of Er and Pr doped ceria pigments: Comparative study. in Processing and Application of Ceramics. 2019;13(3):310-321.
doi:10.2298/PAC1903310M .

Mićović, Dragana, Pagnacco, Maja C., Banković, Predrag, Maletaškić, Jelena, Matović, Branko, Đokić, Veljko, Stojmenović, Marija, "The influence of short thermal treatment on structure, morphology and optical properties of Er and Pr doped ceria pigments: Comparative study" in Processing and Application of Ceramics, 13, no. 3 (2019):310-321,
https://doi.org/10.2298/PAC1903310M . .

TY  - JOUR
AU  - Mirković, Jelena
AU  - Božić, Bojan
AU  - Vitnik, Vesna
AU  - Vitnik, Željko
AU  - Rogan, Jelena
AU  - Poleti, Dejan
AU  - Ušćumlić, Gordana
AU  - Mijin, Dušan
PY  - 2018
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3972
AB  - Ten 5-(substituted phenylazo)-3-cyano-1-ethyl-6-hydroxy-4-methyl-2-pyridones were studied (five new compounds) to provide insight into the electronic effects of diverse substituents located at different positions in their phenyl moieties. The structural features of these dyes were examined by combining experimental and theoretical approaches. The crystal structures of two derivatives were revealed by X-ray crystallography and diverse packing modes owing to different intermolecular interactions (- stacking and lone pair- interactions, as well as hydrogen bonds) were found. A study on lattice energy and energy related to the molecular pairs obtained from their crystal packing was performed. The tautomerism and ionisation of the dyes in ethanol or N,N -dimethylformamide solution were rationalised in terms of diazo component substitution pattern.
PB  - Wiley, Hoboken
T2  - Coloration Technology
T1  - Structural, spectroscopic and computational study of 5-(substituted phenylazo)-3-cyano-1-ethyl-6-hydroxy-4-methyl-2-pyridones
EP  - 43
IS  - 1
SP  - 33
VL  - 134
DO  - 10.1111/cote.12321
ER  - 

@article{
author = "Mirković, Jelena and Božić, Bojan and Vitnik, Vesna and Vitnik, Željko and Rogan, Jelena and Poleti, Dejan and Ušćumlić, Gordana and Mijin, Dušan",
year = "2018",
abstract = "Ten 5-(substituted phenylazo)-3-cyano-1-ethyl-6-hydroxy-4-methyl-2-pyridones were studied (five new compounds) to provide insight into the electronic effects of diverse substituents located at different positions in their phenyl moieties. The structural features of these dyes were examined by combining experimental and theoretical approaches. The crystal structures of two derivatives were revealed by X-ray crystallography and diverse packing modes owing to different intermolecular interactions (- stacking and lone pair- interactions, as well as hydrogen bonds) were found. A study on lattice energy and energy related to the molecular pairs obtained from their crystal packing was performed. The tautomerism and ionisation of the dyes in ethanol or N,N -dimethylformamide solution were rationalised in terms of diazo component substitution pattern.",
publisher = "Wiley, Hoboken",
journal = "Coloration Technology",
title = "Structural, spectroscopic and computational study of 5-(substituted phenylazo)-3-cyano-1-ethyl-6-hydroxy-4-methyl-2-pyridones",
pages = "43-33",
number = "1",
volume = "134",
doi = "10.1111/cote.12321"
}

Mirković, J., Božić, B., Vitnik, V., Vitnik, Ž., Rogan, J., Poleti, D., Ušćumlić, G.,& Mijin, D.. (2018). Structural, spectroscopic and computational study of 5-(substituted phenylazo)-3-cyano-1-ethyl-6-hydroxy-4-methyl-2-pyridones. in Coloration Technology
Wiley, Hoboken., 134(1), 33-43.
https://doi.org/10.1111/cote.12321

Mirković J, Božić B, Vitnik V, Vitnik Ž, Rogan J, Poleti D, Ušćumlić G, Mijin D. Structural, spectroscopic and computational study of 5-(substituted phenylazo)-3-cyano-1-ethyl-6-hydroxy-4-methyl-2-pyridones. in Coloration Technology. 2018;134(1):33-43.
doi:10.1111/cote.12321 .

Mirković, Jelena, Božić, Bojan, Vitnik, Vesna, Vitnik, Željko, Rogan, Jelena, Poleti, Dejan, Ušćumlić, Gordana, Mijin, Dušan, "Structural, spectroscopic and computational study of 5-(substituted phenylazo)-3-cyano-1-ethyl-6-hydroxy-4-methyl-2-pyridones" in Coloration Technology, 134, no. 1 (2018):33-43,
https://doi.org/10.1111/cote.12321 . .

TY  - CONF
AU  - Radovanović, Lidija
AU  - Vulić, Predrag
AU  - Jagličić, Zvonko
AU  - Radovanović, Željko
AU  - Zeković, Ivana
AU  - Rogan, Jelena
PY  - 2018
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6699
AB  - Reakcijom izmene liganada sintetisan je dvofazni materijal I izgrađen od kompleksa
[Mn(dipya)(H2O)4](tpht) i {[Zn(dipya)(tpht)]·H2O}n(tpht = anjon tereftalne kiseline,
dipya = 2,2’-dipiridilamin) i okarakterisan je rendgenskom difrakcijom praha (XRPD),
elementarnom analizom i IC-spektroskopijom. Ritveldovom metodom utvrđena je
struktura obe faze na osnovu poznatih kristalnih struktura kompleksa
[Mn(dipya)(H2O)4](tpht) (monokliničan sistem, prostorna grupa P21/c, a = 7,62769(7),
b = 23,8578(2), c = 11,09364(20) Å, β = 102,2997(10) °) i {[Zn(dipya)(tpht)]·H2O}n
(monokliničan sistem, prostorna grupa P21/n, a = 9,83498(12), b = 14,40421(15),
c = 12,27228(16) Å, β = 95,7954(9) °), koje su određene rendgenskom strukturnom
analizom [1, 2]. Odnos faza [Mn(dipya)(H2O)4](tpht) i {[Zn(dipya)(tpht)]·H2O}n u I
iznosio je 31:69 mas. %. Rezultati utačnjavanja Ritveldovom metodom u dobroj su
saglasnosti, sa neznatnim odstupanjem od strukturnih parametara originalnih struktura:
Rp: 4,28, Rwp: 5,60, Rexp: 4,42, χ
2
: 1,60, RB: 2,39, Rf: 1,99 za Mn(II)-fazu i RB: 3,15,
Rf: 3,13 za Zn(II)-fazu. Mn(II)-fazu obrazuju diskretne kompleksne jedinke
[Mn(dipya)(H2O)4](tpht) u kojima tpht ima ulogu jona suprotnog naelektrisanja sa
deformisano-oktaedarskom geometrijom Mn(II)-jona. Zn(II)-faza izgrađena je od cikcak lanaca {[Zn(dipya)(tpht)]·H2O}n, sa dva kristalografski različita mostovna tphtliganda: bis-helatnim i bis-monodentatnim. Zn(II)-jon se nalazi u deformisanom
kvadratno-piramidalnom okruženju. Termičko ponašanje I ispitano je simultanom
TG/DSC-analizom u atmosferi vazduha i azota. XRPD identifikacija čvrstog ostatka
nakon analize u atmosferi vazduha pokazala je prisustvo dve faze: ZnO (ICDD PDF 36-
1451) i ZnMn2O4 (ICDD PDF 24-1123), čija je morfologija ispitana skenirajućom
elektronskom mikroskopijom (SEM). Merenjem magnetne susceptibilnosti na niskim
temperaturama utvrđene su magnetne interakcije u I i analizirana su fotoluminescentna
svojstva na sobnoj temperaturi.
AB  - A biphasic material I that is composed of complexes [Mn(dipya)(H2O)4](tpht) and
{[Zn(dipya)(tpht)]·H2O}n(tpht = anion of terephthalic acid, dipya = 2,2’-dipyridylamine)
has been synthesized by the ligand exchange reaction and characterized by X-ray powder
diffraction (XRPD), elemental analysis and IR spectroscopy. The structural
characterization of each phase was performed by Rietveld method according to the
known crystal structures of [Mn(dipya)(H2O)4](tpht) (monoclinic, space group P21/c,
a = 7,62769(7), b = 23,8578(2), c = 11,09364(20) Å, β = 102,2997(10) °) and
{[Zn(dipya)(tpht)]·H2O}n (monoclinic, space group P21/n, a = 9,83498(12),
b = 14,40421(15), c = 12,27228(16) Å, β = 95,7954(9) °) determined from single crystal
data [1, 2]. [Mn(dipya)(H2O)4](tpht) to {[Zn(dipya)(tpht)]·H2O}n phase-ratio in I was
31:69 wt. %. The Rietveld refinement results were in a good agreement with a minor
deviation of the final structural parameters from the original structures: Rp: 4.28,
Rwp: 5.60, Rexp: 4.42, χ
2
: 1.60, RB: 2.39, Rf: 1.99 for the Mn(II)-phase, and RB: 3.15,
Rf: 3.13 for the Zn(II)-phase. The Mn(II)-phase consists of discrete complex units
[Mn(dipya)(H2O)4](tpht) in which the tpht is counter anion and with distorted octahedral
geometry of Mn(II) ion. The Zn(II)-phase is comprised of zigzag chains of
{[Zn(dipya)(tpht)]·H2O}n, with two crystallographically different tpht bridges: bischelate and bis-monodentate and Zn(II) ion in a distorted square pyramidal environment.
The thermal behavior of I was studied by simultaneous TG/DSC analysis in both air and
N2 atmospheres. XRPD identification of the solid residue after analysis in air atmosphere
confirmed the presence of two phases: ZnO (ICDD PDF 36-1451) and ZnMn2O4
(ICDD PDF 24-1123), whose morphologies were analyzed using scanning electron
microscopy (SEM). The magnetic susceptibility measurements at low temperatures of I
were performed in order to examine the magnetic interactions and photoluminescence
properties at room temperature have been investigated.
PB  - Beograd : Srpsko kristalografsko društvo = Serbian Crystallographic Society
C3  - Izvodi radova / XXV konferencija Srpskog kristalografskog društva = Abstracts / 25th Conference of the Serbian Crystallographic Society, Bajina Bašta, 21-23. jun 2018
T1  - SINTEZA, STRUKTURA I SVOJSTVA DVOFAZNOG Mn(II)/Zn(II) MATERIJALA
T1  - SYNTHESIS, STRUCTURE AND PROPERTIES OF Mn(II)/Zn(II) BIPHASIC MATERIAL
EP  - 87
SP  - 86
UR  - https://hdl.handle.net/21.15107/rcub_technorep_6699
ER  - 

@conference{
author = "Radovanović, Lidija and Vulić, Predrag and Jagličić, Zvonko and Radovanović, Željko and Zeković, Ivana and Rogan, Jelena",
year = "2018",
abstract = "Reakcijom izmene liganada sintetisan je dvofazni materijal I izgrađen od kompleksa
[Mn(dipya)(H2O)4](tpht) i {[Zn(dipya)(tpht)]·H2O}n(tpht = anjon tereftalne kiseline,
dipya = 2,2’-dipiridilamin) i okarakterisan je rendgenskom difrakcijom praha (XRPD),
elementarnom analizom i IC-spektroskopijom. Ritveldovom metodom utvrđena je
struktura obe faze na osnovu poznatih kristalnih struktura kompleksa
[Mn(dipya)(H2O)4](tpht) (monokliničan sistem, prostorna grupa P21/c, a = 7,62769(7),
b = 23,8578(2), c = 11,09364(20) Å, β = 102,2997(10) °) i {[Zn(dipya)(tpht)]·H2O}n
(monokliničan sistem, prostorna grupa P21/n, a = 9,83498(12), b = 14,40421(15),
c = 12,27228(16) Å, β = 95,7954(9) °), koje su određene rendgenskom strukturnom
analizom [1, 2]. Odnos faza [Mn(dipya)(H2O)4](tpht) i {[Zn(dipya)(tpht)]·H2O}n u I
iznosio je 31:69 mas. %. Rezultati utačnjavanja Ritveldovom metodom u dobroj su
saglasnosti, sa neznatnim odstupanjem od strukturnih parametara originalnih struktura:
Rp: 4,28, Rwp: 5,60, Rexp: 4,42, χ
2
: 1,60, RB: 2,39, Rf: 1,99 za Mn(II)-fazu i RB: 3,15,
Rf: 3,13 za Zn(II)-fazu. Mn(II)-fazu obrazuju diskretne kompleksne jedinke
[Mn(dipya)(H2O)4](tpht) u kojima tpht ima ulogu jona suprotnog naelektrisanja sa
deformisano-oktaedarskom geometrijom Mn(II)-jona. Zn(II)-faza izgrađena je od cikcak lanaca {[Zn(dipya)(tpht)]·H2O}n, sa dva kristalografski različita mostovna tphtliganda: bis-helatnim i bis-monodentatnim. Zn(II)-jon se nalazi u deformisanom
kvadratno-piramidalnom okruženju. Termičko ponašanje I ispitano je simultanom
TG/DSC-analizom u atmosferi vazduha i azota. XRPD identifikacija čvrstog ostatka
nakon analize u atmosferi vazduha pokazala je prisustvo dve faze: ZnO (ICDD PDF 36-
1451) i ZnMn2O4 (ICDD PDF 24-1123), čija je morfologija ispitana skenirajućom
elektronskom mikroskopijom (SEM). Merenjem magnetne susceptibilnosti na niskim
temperaturama utvrđene su magnetne interakcije u I i analizirana su fotoluminescentna
svojstva na sobnoj temperaturi., A biphasic material I that is composed of complexes [Mn(dipya)(H2O)4](tpht) and
{[Zn(dipya)(tpht)]·H2O}n(tpht = anion of terephthalic acid, dipya = 2,2’-dipyridylamine)
has been synthesized by the ligand exchange reaction and characterized by X-ray powder
diffraction (XRPD), elemental analysis and IR spectroscopy. The structural
characterization of each phase was performed by Rietveld method according to the
known crystal structures of [Mn(dipya)(H2O)4](tpht) (monoclinic, space group P21/c,
a = 7,62769(7), b = 23,8578(2), c = 11,09364(20) Å, β = 102,2997(10) °) and
{[Zn(dipya)(tpht)]·H2O}n (monoclinic, space group P21/n, a = 9,83498(12),
b = 14,40421(15), c = 12,27228(16) Å, β = 95,7954(9) °) determined from single crystal
data [1, 2]. [Mn(dipya)(H2O)4](tpht) to {[Zn(dipya)(tpht)]·H2O}n phase-ratio in I was
31:69 wt. %. The Rietveld refinement results were in a good agreement with a minor
deviation of the final structural parameters from the original structures: Rp: 4.28,
Rwp: 5.60, Rexp: 4.42, χ
2
: 1.60, RB: 2.39, Rf: 1.99 for the Mn(II)-phase, and RB: 3.15,
Rf: 3.13 for the Zn(II)-phase. The Mn(II)-phase consists of discrete complex units
[Mn(dipya)(H2O)4](tpht) in which the tpht is counter anion and with distorted octahedral
geometry of Mn(II) ion. The Zn(II)-phase is comprised of zigzag chains of
{[Zn(dipya)(tpht)]·H2O}n, with two crystallographically different tpht bridges: bischelate and bis-monodentate and Zn(II) ion in a distorted square pyramidal environment.
The thermal behavior of I was studied by simultaneous TG/DSC analysis in both air and
N2 atmospheres. XRPD identification of the solid residue after analysis in air atmosphere
confirmed the presence of two phases: ZnO (ICDD PDF 36-1451) and ZnMn2O4
(ICDD PDF 24-1123), whose morphologies were analyzed using scanning electron
microscopy (SEM). The magnetic susceptibility measurements at low temperatures of I
were performed in order to examine the magnetic interactions and photoluminescence
properties at room temperature have been investigated.",
publisher = "Beograd : Srpsko kristalografsko društvo = Serbian Crystallographic Society",
journal = "Izvodi radova / XXV konferencija Srpskog kristalografskog društva = Abstracts / 25th Conference of the Serbian Crystallographic Society, Bajina Bašta, 21-23. jun 2018",
title = "SINTEZA, STRUKTURA I SVOJSTVA DVOFAZNOG Mn(II)/Zn(II) MATERIJALA, SYNTHESIS, STRUCTURE AND PROPERTIES OF Mn(II)/Zn(II) BIPHASIC MATERIAL",
pages = "87-86",
url = "https://hdl.handle.net/21.15107/rcub_technorep_6699"
}

Radovanović, L., Vulić, P., Jagličić, Z., Radovanović, Ž., Zeković, I.,& Rogan, J.. (2018). SINTEZA, STRUKTURA I SVOJSTVA DVOFAZNOG Mn(II)/Zn(II) MATERIJALA. in Izvodi radova / XXV konferencija Srpskog kristalografskog društva = Abstracts / 25th Conference of the Serbian Crystallographic Society, Bajina Bašta, 21-23. jun 2018
Beograd : Srpsko kristalografsko društvo = Serbian Crystallographic Society., 86-87.
https://hdl.handle.net/21.15107/rcub_technorep_6699

Radovanović L, Vulić P, Jagličić Z, Radovanović Ž, Zeković I, Rogan J. SINTEZA, STRUKTURA I SVOJSTVA DVOFAZNOG Mn(II)/Zn(II) MATERIJALA. in Izvodi radova / XXV konferencija Srpskog kristalografskog društva = Abstracts / 25th Conference of the Serbian Crystallographic Society, Bajina Bašta, 21-23. jun 2018. 2018;:86-87.
https://hdl.handle.net/21.15107/rcub_technorep_6699 .

Radovanović, Lidija, Vulić, Predrag, Jagličić, Zvonko, Radovanović, Željko, Zeković, Ivana, Rogan, Jelena, "SINTEZA, STRUKTURA I SVOJSTVA DVOFAZNOG Mn(II)/Zn(II) MATERIJALA" in Izvodi radova / XXV konferencija Srpskog kristalografskog društva = Abstracts / 25th Conference of the Serbian Crystallographic Society, Bajina Bašta, 21-23. jun 2018 (2018):86-87,
https://hdl.handle.net/21.15107/rcub_technorep_6699 .

TY  - JOUR
AU  - Radojković, Aleksandar
AU  - Luković-Golić, Danijela
AU  - Ćirković, Jovana
AU  - Marinković-Stanojević, Zorica
AU  - Pajić, Damir
AU  - Torić, Filip
AU  - Dapčević, Aleksandra
AU  - Vulić, Predrag
AU  - Branković, Zorica
AU  - Branković, Goran
PY  - 2018
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3856
AB  - Bulk ceramic samples of BiFeO3 were light doped (up to 1%) with Nb5+ in the place of Fe3+ (B-site doping) and their multiferroic properties were investigated using XRD, SEM, polarization (PMTS) and magnetization (SQUID) techniques. It is shown that even the small percentages of doping can notably change electric and magnetic behavior. Electric conductivity differs by two orders of magnitude between samples doped with 0.2% and 1% Nb. The ferroelectric behavior strongly depended on conduction mechanism, and transition from space-charge-limited current (SCLC) conduction to trap-filled limited (TFL) conduction regime reflected on a change in hysteresis patterns, particularly for the samples with 0.2% and 0.5% Nb. Separation of ZFC-FC magnetization curves occurred for all Nb concentrations and increased with Nb doping. Weak ferromagnetic behavior and the increase of remnant magnetization with Nb concentration was observed from the hysteresis measurements. Coercive field changed drastically compared to the pure BiFeO3, namely, the sample with 1% Nb exhibited very high coercive magnetic field of 10 kOe.
PB  - Elsevier Sci Ltd, Oxford
T2  - Ceramics International
T1  - Tuning of BiFeO3 multiferroic properties by light doping with Nb
EP  - 16744
IS  - 14
SP  - 16739
VL  - 44
DO  - 10.1016/j.ceramint.2018.06.103
ER  - 

@article{
author = "Radojković, Aleksandar and Luković-Golić, Danijela and Ćirković, Jovana and Marinković-Stanojević, Zorica and Pajić, Damir and Torić, Filip and Dapčević, Aleksandra and Vulić, Predrag and Branković, Zorica and Branković, Goran",
year = "2018",
abstract = "Bulk ceramic samples of BiFeO3 were light doped (up to 1%) with Nb5+ in the place of Fe3+ (B-site doping) and their multiferroic properties were investigated using XRD, SEM, polarization (PMTS) and magnetization (SQUID) techniques. It is shown that even the small percentages of doping can notably change electric and magnetic behavior. Electric conductivity differs by two orders of magnitude between samples doped with 0.2% and 1% Nb. The ferroelectric behavior strongly depended on conduction mechanism, and transition from space-charge-limited current (SCLC) conduction to trap-filled limited (TFL) conduction regime reflected on a change in hysteresis patterns, particularly for the samples with 0.2% and 0.5% Nb. Separation of ZFC-FC magnetization curves occurred for all Nb concentrations and increased with Nb doping. Weak ferromagnetic behavior and the increase of remnant magnetization with Nb concentration was observed from the hysteresis measurements. Coercive field changed drastically compared to the pure BiFeO3, namely, the sample with 1% Nb exhibited very high coercive magnetic field of 10 kOe.",
publisher = "Elsevier Sci Ltd, Oxford",
journal = "Ceramics International",
title = "Tuning of BiFeO3 multiferroic properties by light doping with Nb",
pages = "16744-16739",
number = "14",
volume = "44",
doi = "10.1016/j.ceramint.2018.06.103"
}

Radojković, A., Luković-Golić, D., Ćirković, J., Marinković-Stanojević, Z., Pajić, D., Torić, F., Dapčević, A., Vulić, P., Branković, Z.,& Branković, G.. (2018). Tuning of BiFeO3 multiferroic properties by light doping with Nb. in Ceramics International
Elsevier Sci Ltd, Oxford., 44(14), 16739-16744.
https://doi.org/10.1016/j.ceramint.2018.06.103

Radojković A, Luković-Golić D, Ćirković J, Marinković-Stanojević Z, Pajić D, Torić F, Dapčević A, Vulić P, Branković Z, Branković G. Tuning of BiFeO3 multiferroic properties by light doping with Nb. in Ceramics International. 2018;44(14):16739-16744.
doi:10.1016/j.ceramint.2018.06.103 .

Radojković, Aleksandar, Luković-Golić, Danijela, Ćirković, Jovana, Marinković-Stanojević, Zorica, Pajić, Damir, Torić, Filip, Dapčević, Aleksandra, Vulić, Predrag, Branković, Zorica, Branković, Goran, "Tuning of BiFeO3 multiferroic properties by light doping with Nb" in Ceramics International, 44, no. 14 (2018):16739-16744,
https://doi.org/10.1016/j.ceramint.2018.06.103 . .

TY  - JOUR
AU  - Filipović, Suzana
AU  - Obradović, Nina
AU  - Marković, Smilja
AU  - Đorđević, Antonije
AU  - Balać, Igor
AU  - Dapčević, Aleksandra
AU  - Rogan, Jelena
AU  - Pavlović, Vladimir B.
PY  - 2018
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3909
AB  - Corundum (alpha-alumina) is a suiTab. material for usage in various industry fields owing to its chemical stability, electrical and mechanical features. It is known that properties of ceramics could be modified by addition of different oxides, as well as by changing the consolidation parameters. In this respect, alumina was doped with 1 wt.% of Cr2O3, Mn2O3 and NiO, followed by 1 hour of mechanical activation in a high-energy planetary ball mill. A sensitive dilatometer was used for sintering of powder mixtures up to 1400 degrees C and recording the obtained dilatation. The final density varied between cca. 1.9 and 3.3 g/cm(3). Microstructural changes were detected by SEM measurements. Changes in electrical permittivity and loss tangent were associated with the preparation conditions (types of additives, duration of mechanical activation). For a given mixture, the sintering increases the relative permittivity and decreases losses, exhibiting the optimal values of 8.32 and 0.027, respectively, for the sample activated 60 minutes and sintered, with the addition of MnO2. Mechanical measurements indicate significant differences in strength with the addition of different transition metal oxides. Samples with Mn and Ni, activated and sintered, with strength of 121 and 86 MPa, respectively, have a significantly higher tensile strength than the other tested samples, due to their more compact microstructures.
PB  - Međunarodni Institut za nauku o sinterovanju, Beograd
T2  - Science of Sintering
T1  - Physical Properties of Sintered Alumina Doped with Different Oxides
EP  - 419
IS  - 4
SP  - 409
VL  - 50
DO  - 10.2298/SOS1804409F
ER  - 

@article{
author = "Filipović, Suzana and Obradović, Nina and Marković, Smilja and Đorđević, Antonije and Balać, Igor and Dapčević, Aleksandra and Rogan, Jelena and Pavlović, Vladimir B.",
year = "2018",
abstract = "Corundum (alpha-alumina) is a suiTab. material for usage in various industry fields owing to its chemical stability, electrical and mechanical features. It is known that properties of ceramics could be modified by addition of different oxides, as well as by changing the consolidation parameters. In this respect, alumina was doped with 1 wt.% of Cr2O3, Mn2O3 and NiO, followed by 1 hour of mechanical activation in a high-energy planetary ball mill. A sensitive dilatometer was used for sintering of powder mixtures up to 1400 degrees C and recording the obtained dilatation. The final density varied between cca. 1.9 and 3.3 g/cm(3). Microstructural changes were detected by SEM measurements. Changes in electrical permittivity and loss tangent were associated with the preparation conditions (types of additives, duration of mechanical activation). For a given mixture, the sintering increases the relative permittivity and decreases losses, exhibiting the optimal values of 8.32 and 0.027, respectively, for the sample activated 60 minutes and sintered, with the addition of MnO2. Mechanical measurements indicate significant differences in strength with the addition of different transition metal oxides. Samples with Mn and Ni, activated and sintered, with strength of 121 and 86 MPa, respectively, have a significantly higher tensile strength than the other tested samples, due to their more compact microstructures.",
publisher = "Međunarodni Institut za nauku o sinterovanju, Beograd",
journal = "Science of Sintering",
title = "Physical Properties of Sintered Alumina Doped with Different Oxides",
pages = "419-409",
number = "4",
volume = "50",
doi = "10.2298/SOS1804409F"
}

Filipović, S., Obradović, N., Marković, S., Đorđević, A., Balać, I., Dapčević, A., Rogan, J.,& Pavlović, V. B.. (2018). Physical Properties of Sintered Alumina Doped with Different Oxides. in Science of Sintering
Međunarodni Institut za nauku o sinterovanju, Beograd., 50(4), 409-419.
https://doi.org/10.2298/SOS1804409F

Filipović S, Obradović N, Marković S, Đorđević A, Balać I, Dapčević A, Rogan J, Pavlović VB. Physical Properties of Sintered Alumina Doped with Different Oxides. in Science of Sintering. 2018;50(4):409-419.
doi:10.2298/SOS1804409F .

Filipović, Suzana, Obradović, Nina, Marković, Smilja, Đorđević, Antonije, Balać, Igor, Dapčević, Aleksandra, Rogan, Jelena, Pavlović, Vladimir B., "Physical Properties of Sintered Alumina Doped with Different Oxides" in Science of Sintering, 50, no. 4 (2018):409-419,
https://doi.org/10.2298/SOS1804409F . .

TY  - THES
AU  - Radovanović, Lidija D.
PY  - 2018
UR  - http://eteze.bg.ac.rs/application/showtheses?thesesId=6246
UR  - https://fedorabg.bg.ac.rs/fedora/get/o:18860/bdef:Content/download
UR  - http://vbs.rs/scripts/cobiss?command=DISPLAY&base=70036&RID=50655759
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4674
AB  - Reakcijom izmene liganada različitim metodama sinteze dobijeno je 22 ternarna kompleksa elemenata d-bloka [Mn(II), Co(II), Ni(II), Cu(II) i Zn(II)] sa anjonima aromatičnih polikarboksilnih kiselina (ftalne, izoftalne, tereftalne i piromelitne) kao O,O-donorskim ligandima i aromatičnim N,N-donorskim ligandima kao što su 2,2'-dipiridilamin i 2,2'-bipirimidin. Trinaest kompleksa sintetisano je u monokristalnom obliku, dok su ostala jedinjenja mikrokristalna. Prema vrsti centralnog atoma, u obliku monokristala dobijeno je pet Mn(II)-, dva Co(II)-, jedan Ni(II)-, dva Cu(II)-, dva Zn(II)-kompleksa, kao i bimetalni Mn(II)–Cu(II)-kompleks...
AB  - A series of 22 d-block element complexes [Mn(II), Co(II), Ni(II), Cu(II) and Zn(II)] containing anions of aromatic polycarboxylate acids (phthalic, isophthalic, terephthalic and pyromellic) as O,O-donor ligands and aromatic N,N-donor ligands such as 2,2'-dipyridylamine and 2,2'-bipyrimidine, has been obtained by ligand exchange reaction using different synthetic methods. Thirteen complexes were obtained as single crystals, while the others were microcrystalline powders. According to the type of central atom, five Mn(II), two Co(II), one Ni(II), two Cu(II), two Zn(II) complexes, and bimetallic Mn(II)–Cu(II) complex were synthesized in form of single crystals. The structures of these compounds were determined by single-crystal X-ray analysis. Structural properties of complexes were discussed in detail and compared...
PB  - Univerzitet u Beogradu, Tehnološko-metalurški fakultet
T1  - Kompleksi elemenata d-bloka sa aromatičnim O,O- I N, N-donorskim ligandima: sinteza, struktura, svojstva i primena
T1  - Complexes of d-block elements with aromatic o,o- and n,n-donor ligands: synthesis, structure, properties and applications
UR  - https://hdl.handle.net/21.15107/rcub_technorep_4674
ER  - 

@phdthesis{
author = "Radovanović, Lidija D.",
year = "2018",
abstract = "Reakcijom izmene liganada različitim metodama sinteze dobijeno je 22 ternarna kompleksa elemenata d-bloka [Mn(II), Co(II), Ni(II), Cu(II) i Zn(II)] sa anjonima aromatičnih polikarboksilnih kiselina (ftalne, izoftalne, tereftalne i piromelitne) kao O,O-donorskim ligandima i aromatičnim N,N-donorskim ligandima kao što su 2,2'-dipiridilamin i 2,2'-bipirimidin. Trinaest kompleksa sintetisano je u monokristalnom obliku, dok su ostala jedinjenja mikrokristalna. Prema vrsti centralnog atoma, u obliku monokristala dobijeno je pet Mn(II)-, dva Co(II)-, jedan Ni(II)-, dva Cu(II)-, dva Zn(II)-kompleksa, kao i bimetalni Mn(II)–Cu(II)-kompleks..., A series of 22 d-block element complexes [Mn(II), Co(II), Ni(II), Cu(II) and Zn(II)] containing anions of aromatic polycarboxylate acids (phthalic, isophthalic, terephthalic and pyromellic) as O,O-donor ligands and aromatic N,N-donor ligands such as 2,2'-dipyridylamine and 2,2'-bipyrimidine, has been obtained by ligand exchange reaction using different synthetic methods. Thirteen complexes were obtained as single crystals, while the others were microcrystalline powders. According to the type of central atom, five Mn(II), two Co(II), one Ni(II), two Cu(II), two Zn(II) complexes, and bimetallic Mn(II)–Cu(II) complex were synthesized in form of single crystals. The structures of these compounds were determined by single-crystal X-ray analysis. Structural properties of complexes were discussed in detail and compared...",
publisher = "Univerzitet u Beogradu, Tehnološko-metalurški fakultet",
title = "Kompleksi elemenata d-bloka sa aromatičnim O,O- I N, N-donorskim ligandima: sinteza, struktura, svojstva i primena, Complexes of d-block elements with aromatic o,o- and n,n-donor ligands: synthesis, structure, properties and applications",
url = "https://hdl.handle.net/21.15107/rcub_technorep_4674"
}

Radovanović, L. D.. (2018). Kompleksi elemenata d-bloka sa aromatičnim O,O- I N, N-donorskim ligandima: sinteza, struktura, svojstva i primena. 
Univerzitet u Beogradu, Tehnološko-metalurški fakultet..
https://hdl.handle.net/21.15107/rcub_technorep_4674

Radovanović LD. Kompleksi elemenata d-bloka sa aromatičnim O,O- I N, N-donorskim ligandima: sinteza, struktura, svojstva i primena. 2018;.
https://hdl.handle.net/21.15107/rcub_technorep_4674 .

Radovanović, Lidija D., "Kompleksi elemenata d-bloka sa aromatičnim O,O- I N, N-donorskim ligandima: sinteza, struktura, svojstva i primena" (2018),
https://hdl.handle.net/21.15107/rcub_technorep_4674 .

TY  - CONF
AU  - Radovanović, Lidija
AU  - Vulić, Predrag
AU  - Radovanović, Željko
AU  - Balanč, Bojana
AU  - Simović, Bojana
AU  - Zeković, Ivana
AU  - Dramićanin, Miroslav
AU  - Rogan, Jelena
PY  - 2018
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3800
AB  - Transition metal oxides are important materials that have found many applications,
as capacitors, sensors or in energy storage [1]. Synthesis of these compounds
has been realized by various methods, such as hydro(solvo)thermal synthesis,
precipitation, microwave synthesis or sol-gel synthesis [2]. Recently, the thermolysis
of coordination compounds as precursors has been considered as a new approach in
obtaining functional nanosized materials. [3]. In this way, by selecting the proper
precursor, it is possible to control the phase composition, morphology and particle
size of a resulting material [3]. The biphasic powder composed of ZnO (zincite) and ZnMn2O4 (hetaerolite), (I) has been
obtained by thermolysis of bimetallic complex [MnZn2(dipya)3(tpht)3(H2O)4]·2H2O
(dipya = 2,2’-dipyridylamine, tpht = dianion of 1,4-benzenedicarboxylic acid) at
450 °C during 1 h in air atmosphere. Scanning Electron Microscopy (SEM) was
used to investigate the morphology of I (Figure 1). It can be observed that the
morphology consists of deformed spherical grains of ZnO with an average diameter
of 67 nm and elliptical grains of hetaerolite whose average diameter and length
were 156 and 290 nm, respectively. The X-ray powder diffraction (XRPD) was
applied to investigate the structure of I. In Figure 2 two-phase Rietveld refinement pattern of I is presented (ZnO to ZnMn2O4 phase-ratio of 62:38 wt. %). The main
crystallographic data and Rietveld refinement parameters for ZnO phase are:
hexagonal, space group P63mc, a = 3.2574(1), c = 5.2175(2) Å, V = 47.945(3) Å3
; for
ZnMn2O4 phase are: tetragonal, space group I41/amd, a = 5.7299(3), c = 9.3000(8) Å,
V = 305.34(3) Å3
; Rwp = 4.80 %, Rp = 3.82 %, Rexp = 3.80 % and χ2
 = 1.5960. UVVis-NIR absorption spectrum was measured in order to investigate the direct band
gap (Eg) of I. Due to the existence of two phases in I, two different Eg values of
2.4 and 3.3 eV for ZnMn2O4 and ZnO phase, respectively, were determined using
Kubelka-Munk function. The mean size, polydispersity index (PDI) and zeta
potential of spherical grains were measured using Zetasizer Nano Series, Nano ZS.
The mean size was 418.6±53.1 nm while PDI value was found to be 0.354±0.099.
Relatively high values of PDI and low apostate value of zeta potential (–6.55 mV)
are indications of incipient instability of colloidal dispersion of I, probably due to the
formation of agglomerates [4, 5]. Photoluminescence measurements were carried
out at room temperature on Fluorolog-3 Model FL3-221 spectrofluorimeter system
upon excitation at 350 nm, in order to study the optical properties of I. This analysis
revealed one band centred at 422 nm in the blue region of the visible part of the
spectrum, which can possibly be associated with defects in the crystal structure of
the ZnO phase [6].
PB  - Belgrade : Serbian Academy of Sciences and Arts
C3  - Program and Book of Abstracts / First International Conference on Electron Microscopy of Nanostructures ELMINA 2018, August 27-29, 2018, Belgrade, Serbia
T1  - Synthesis, Structure, Morphology and Properties of Biphasic ZnO–ZnMn2O4
EP  - 173
SP  - 171
UR  - https://hdl.handle.net/21.15107/rcub_vinar_8737
ER  - 

@conference{
author = "Radovanović, Lidija and Vulić, Predrag and Radovanović, Željko and Balanč, Bojana and Simović, Bojana and Zeković, Ivana and Dramićanin, Miroslav and Rogan, Jelena",
year = "2018",
abstract = "Transition metal oxides are important materials that have found many applications,
as capacitors, sensors or in energy storage [1]. Synthesis of these compounds
has been realized by various methods, such as hydro(solvo)thermal synthesis,
precipitation, microwave synthesis or sol-gel synthesis [2]. Recently, the thermolysis
of coordination compounds as precursors has been considered as a new approach in
obtaining functional nanosized materials. [3]. In this way, by selecting the proper
precursor, it is possible to control the phase composition, morphology and particle
size of a resulting material [3]. The biphasic powder composed of ZnO (zincite) and ZnMn2O4 (hetaerolite), (I) has been
obtained by thermolysis of bimetallic complex [MnZn2(dipya)3(tpht)3(H2O)4]·2H2O
(dipya = 2,2’-dipyridylamine, tpht = dianion of 1,4-benzenedicarboxylic acid) at
450 °C during 1 h in air atmosphere. Scanning Electron Microscopy (SEM) was
used to investigate the morphology of I (Figure 1). It can be observed that the
morphology consists of deformed spherical grains of ZnO with an average diameter
of 67 nm and elliptical grains of hetaerolite whose average diameter and length
were 156 and 290 nm, respectively. The X-ray powder diffraction (XRPD) was
applied to investigate the structure of I. In Figure 2 two-phase Rietveld refinement pattern of I is presented (ZnO to ZnMn2O4 phase-ratio of 62:38 wt. %). The main
crystallographic data and Rietveld refinement parameters for ZnO phase are:
hexagonal, space group P63mc, a = 3.2574(1), c = 5.2175(2) Å, V = 47.945(3) Å3
; for
ZnMn2O4 phase are: tetragonal, space group I41/amd, a = 5.7299(3), c = 9.3000(8) Å,
V = 305.34(3) Å3
; Rwp = 4.80 %, Rp = 3.82 %, Rexp = 3.80 % and χ2
 = 1.5960. UVVis-NIR absorption spectrum was measured in order to investigate the direct band
gap (Eg) of I. Due to the existence of two phases in I, two different Eg values of
2.4 and 3.3 eV for ZnMn2O4 and ZnO phase, respectively, were determined using
Kubelka-Munk function. The mean size, polydispersity index (PDI) and zeta
potential of spherical grains were measured using Zetasizer Nano Series, Nano ZS.
The mean size was 418.6±53.1 nm while PDI value was found to be 0.354±0.099.
Relatively high values of PDI and low apostate value of zeta potential (–6.55 mV)
are indications of incipient instability of colloidal dispersion of I, probably due to the
formation of agglomerates [4, 5]. Photoluminescence measurements were carried
out at room temperature on Fluorolog-3 Model FL3-221 spectrofluorimeter system
upon excitation at 350 nm, in order to study the optical properties of I. This analysis
revealed one band centred at 422 nm in the blue region of the visible part of the
spectrum, which can possibly be associated with defects in the crystal structure of
the ZnO phase [6].",
publisher = "Belgrade : Serbian Academy of Sciences and Arts",
journal = "Program and Book of Abstracts / First International Conference on Electron Microscopy of Nanostructures ELMINA 2018, August 27-29, 2018, Belgrade, Serbia",
title = "Synthesis, Structure, Morphology and Properties of Biphasic ZnO–ZnMn2O4",
pages = "173-171",
url = "https://hdl.handle.net/21.15107/rcub_vinar_8737"
}

Radovanović, L., Vulić, P., Radovanović, Ž., Balanč, B., Simović, B., Zeković, I., Dramićanin, M.,& Rogan, J.. (2018). Synthesis, Structure, Morphology and Properties of Biphasic ZnO–ZnMn2O4. in Program and Book of Abstracts / First International Conference on Electron Microscopy of Nanostructures ELMINA 2018, August 27-29, 2018, Belgrade, Serbia
Belgrade : Serbian Academy of Sciences and Arts., 171-173.
https://hdl.handle.net/21.15107/rcub_vinar_8737

Radovanović L, Vulić P, Radovanović Ž, Balanč B, Simović B, Zeković I, Dramićanin M, Rogan J. Synthesis, Structure, Morphology and Properties of Biphasic ZnO–ZnMn2O4. in Program and Book of Abstracts / First International Conference on Electron Microscopy of Nanostructures ELMINA 2018, August 27-29, 2018, Belgrade, Serbia. 2018;:171-173.
https://hdl.handle.net/21.15107/rcub_vinar_8737 .

Radovanović, Lidija, Vulić, Predrag, Radovanović, Željko, Balanč, Bojana, Simović, Bojana, Zeković, Ivana, Dramićanin, Miroslav, Rogan, Jelena, "Synthesis, Structure, Morphology and Properties of Biphasic ZnO–ZnMn2O4" in Program and Book of Abstracts / First International Conference on Electron Microscopy of Nanostructures ELMINA 2018, August 27-29, 2018, Belgrade, Serbia (2018):171-173,
https://hdl.handle.net/21.15107/rcub_vinar_8737 .

TY  - JOUR
AU  - Zdravković, Jelena D.
AU  - Radovanović, Lidija
AU  - Poleti, Dejan
AU  - Rogan, Jelena R.
AU  - Vulić, Predrag J.
AU  - Radovanović, Željko
AU  - Minić, Dragica M.
PY  - 2018
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4003
AB  - The design of mixed-ligand complexes are of increasing interest from fundamental as well as technological and curative aspects. Having that in mind, we studied zinc complex containing 2,2'-dipyridylamine (dipya) and dianion of isophthalic acid (ipht), [Zn(dipya)(ipht)](n), as promising precursor for synthesis of nanostructured metal oxide. In that sense, the mechanism and degradation kinetics of [Zn(dipya)(ipht)](n), was analyzed under non-isothermal conditions in nitrogen and in air atmospheres. Peak deconvolution of the [Zn(dipya)(ipht)](n), decomposition profile, in the form of a derivative thermogram (DTG), in nitrogen atmosphere, revealed the presence of three decomposition steps, while in air five single steps were isolated. In both cases ZnO is formed as residue at 530 degrees C: pure (in air) or in amorphous matrix (nitrogen). In air we obtained well crystalized ZnO nanospheres (-25 nm), by thermal treatment in temperature range 370-530 degrees C showing that this complex could be considered as good precursor for production of nanosized ZnO.
PB  - Elsevier Masson SAS
T2  - Solid State Sciences
T1  - Mechanism and degradation kinetics of zinc complex containing isophthalato and 2,2 '-dipyridylamine ligands under different atmospheres
EP  - 131
SP  - 123
VL  - 80
DO  - 10.1016/j.solidstatesciences.2018.04.013
ER  - 

@article{
author = "Zdravković, Jelena D. and Radovanović, Lidija and Poleti, Dejan and Rogan, Jelena R. and Vulić, Predrag J. and Radovanović, Željko and Minić, Dragica M.",
year = "2018",
abstract = "The design of mixed-ligand complexes are of increasing interest from fundamental as well as technological and curative aspects. Having that in mind, we studied zinc complex containing 2,2'-dipyridylamine (dipya) and dianion of isophthalic acid (ipht), [Zn(dipya)(ipht)](n), as promising precursor for synthesis of nanostructured metal oxide. In that sense, the mechanism and degradation kinetics of [Zn(dipya)(ipht)](n), was analyzed under non-isothermal conditions in nitrogen and in air atmospheres. Peak deconvolution of the [Zn(dipya)(ipht)](n), decomposition profile, in the form of a derivative thermogram (DTG), in nitrogen atmosphere, revealed the presence of three decomposition steps, while in air five single steps were isolated. In both cases ZnO is formed as residue at 530 degrees C: pure (in air) or in amorphous matrix (nitrogen). In air we obtained well crystalized ZnO nanospheres (-25 nm), by thermal treatment in temperature range 370-530 degrees C showing that this complex could be considered as good precursor for production of nanosized ZnO.",
publisher = "Elsevier Masson SAS",
journal = "Solid State Sciences",
title = "Mechanism and degradation kinetics of zinc complex containing isophthalato and 2,2 '-dipyridylamine ligands under different atmospheres",
pages = "131-123",
volume = "80",
doi = "10.1016/j.solidstatesciences.2018.04.013"
}

Zdravković, J. D., Radovanović, L., Poleti, D., Rogan, J. R., Vulić, P. J., Radovanović, Ž.,& Minić, D. M.. (2018). Mechanism and degradation kinetics of zinc complex containing isophthalato and 2,2 '-dipyridylamine ligands under different atmospheres. in Solid State Sciences
Elsevier Masson SAS., 80, 123-131.
https://doi.org/10.1016/j.solidstatesciences.2018.04.013

Zdravković JD, Radovanović L, Poleti D, Rogan JR, Vulić PJ, Radovanović Ž, Minić DM. Mechanism and degradation kinetics of zinc complex containing isophthalato and 2,2 '-dipyridylamine ligands under different atmospheres. in Solid State Sciences. 2018;80:123-131.
doi:10.1016/j.solidstatesciences.2018.04.013 .

Zdravković, Jelena D., Radovanović, Lidija, Poleti, Dejan, Rogan, Jelena R., Vulić, Predrag J., Radovanović, Željko, Minić, Dragica M., "Mechanism and degradation kinetics of zinc complex containing isophthalato and 2,2 '-dipyridylamine ligands under different atmospheres" in Solid State Sciences, 80 (2018):123-131,
https://doi.org/10.1016/j.solidstatesciences.2018.04.013 . .