Janjić, Goran V.

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56f4b1de-b15e-4c4a-a63d-f4928ea41e1d
  • Janjić, Goran V. (2)
  • Janjić, Goran (1)
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Author's Bibliography

Cascade luminescence and antibacterial behavior of fluorapatite nanopowder co-doped with Pr3+, NO3− and CO32− ions

Milojkov, Dušan V.; Sokić, Miroslav D.; Živković-Radovanović, Vukosava; Manojlović, Vaso D.; Mutavdžić, Dragosav R.; Janjić, Goran V.; Radotić, Ksenija

(Springer, 2023)

TY  - JOUR
AU  - Milojkov, Dušan V.
AU  - Sokić, Miroslav D.
AU  - Živković-Radovanović, Vukosava
AU  - Manojlović, Vaso D.
AU  - Mutavdžić, Dragosav R.
AU  - Janjić, Goran V.
AU  - Radotić, Ksenija
PY  - 2023
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5279
AB  - In this study, luminescence and antibacterial behavior of pure fluorapatite (FAp) and praseodymium-nitrate-carbonate co-doped fluorapatite (PrNCFAp) nanopowders were investigated. Uniform nanopowders were synthesized by precipitation reaction followed by centrifugation and systematically characterized by XRD, FTIR, SEM–EDS, TG and PL methods. XRD analysis revealed the formation of hexagonal FAp crystals, and FTIR spectra indicate the presence of nitrate (NO3−) and carbonate (CO32−) species. SEM analyzes confirm agglomerates composed of irregular nanometer-sized spheres. Emission of FAp nanopowder occurred in the violet-blue region of the visible part of the spectrum, with redshift to the blue-green color region when Pr3+, NO3− and CO32− co-doped in the lattice. Analysis of luminescence spectra by MCR-ALS method extract three fluorophores from the PrNCFAp sample and showed simultaneous existents of emission-reabsorption-emission between dopants in FAp lattice. Antibacterial activity against pathogen Staphylococcus aureus was investigated before and after treatment of nanopowders by UVA radiation of 365 nm. Nanopowders irradiated with UVA compared to non-irradiated reduced Staphylococcus aureus by 84.9% for PrNCFAp and 33.3% for FAp in the first 0.5 h of contact, and 76.1% and 42.9% after 24 h of contact. In addition, the obtained luminescent nanomaterials showed a low degree of hemolytic activity and could potentially be candidates for further research in dentistry.
PB  - Springer
T2  - Optical and Quantum Electronics
T1  - Cascade luminescence and antibacterial behavior of fluorapatite nanopowder co-doped with Pr3+, NO3− and CO32− ions
IS  - 1
SP  - 84
VL  - 55
DO  - 10.1007/s11082-022-04347-7
ER  - 
@article{
author = "Milojkov, Dušan V. and Sokić, Miroslav D. and Živković-Radovanović, Vukosava and Manojlović, Vaso D. and Mutavdžić, Dragosav R. and Janjić, Goran V. and Radotić, Ksenija",
year = "2023",
abstract = "In this study, luminescence and antibacterial behavior of pure fluorapatite (FAp) and praseodymium-nitrate-carbonate co-doped fluorapatite (PrNCFAp) nanopowders were investigated. Uniform nanopowders were synthesized by precipitation reaction followed by centrifugation and systematically characterized by XRD, FTIR, SEM–EDS, TG and PL methods. XRD analysis revealed the formation of hexagonal FAp crystals, and FTIR spectra indicate the presence of nitrate (NO3−) and carbonate (CO32−) species. SEM analyzes confirm agglomerates composed of irregular nanometer-sized spheres. Emission of FAp nanopowder occurred in the violet-blue region of the visible part of the spectrum, with redshift to the blue-green color region when Pr3+, NO3− and CO32− co-doped in the lattice. Analysis of luminescence spectra by MCR-ALS method extract three fluorophores from the PrNCFAp sample and showed simultaneous existents of emission-reabsorption-emission between dopants in FAp lattice. Antibacterial activity against pathogen Staphylococcus aureus was investigated before and after treatment of nanopowders by UVA radiation of 365 nm. Nanopowders irradiated with UVA compared to non-irradiated reduced Staphylococcus aureus by 84.9% for PrNCFAp and 33.3% for FAp in the first 0.5 h of contact, and 76.1% and 42.9% after 24 h of contact. In addition, the obtained luminescent nanomaterials showed a low degree of hemolytic activity and could potentially be candidates for further research in dentistry.",
publisher = "Springer",
journal = "Optical and Quantum Electronics",
title = "Cascade luminescence and antibacterial behavior of fluorapatite nanopowder co-doped with Pr3+, NO3− and CO32− ions",
number = "1",
pages = "84",
volume = "55",
doi = "10.1007/s11082-022-04347-7"
}
Milojkov, D. V., Sokić, M. D., Živković-Radovanović, V., Manojlović, V. D., Mutavdžić, D. R., Janjić, G. V.,& Radotić, K.. (2023). Cascade luminescence and antibacterial behavior of fluorapatite nanopowder co-doped with Pr3+, NO3− and CO32− ions. in Optical and Quantum Electronics
Springer., 55(1), 84.
https://doi.org/10.1007/s11082-022-04347-7
Milojkov DV, Sokić MD, Živković-Radovanović V, Manojlović VD, Mutavdžić DR, Janjić GV, Radotić K. Cascade luminescence and antibacterial behavior of fluorapatite nanopowder co-doped with Pr3+, NO3− and CO32− ions. in Optical and Quantum Electronics. 2023;55(1):84.
doi:10.1007/s11082-022-04347-7 .
Milojkov, Dušan V., Sokić, Miroslav D., Živković-Radovanović, Vukosava, Manojlović, Vaso D., Mutavdžić, Dragosav R., Janjić, Goran V., Radotić, Ksenija, "Cascade luminescence and antibacterial behavior of fluorapatite nanopowder co-doped with Pr3+, NO3− and CO32− ions" in Optical and Quantum Electronics, 55, no. 1 (2023):84,
https://doi.org/10.1007/s11082-022-04347-7 . .
1

Zamena sumpora selenom. Efekat polarnih grupa iz okruženja

Suručić, Ljiljana; Tadić, Tamara; Nastasović, Aleksandra; Marković, Bojana; Sandić, Zvjezdana; Onjia, Antonije; Janjić, Goran

(Beograd : Srpsko kristalografsko društvo, 2021)

TY  - CONF
AU  - Suručić, Ljiljana
AU  - Tadić, Tamara
AU  - Nastasović, Aleksandra
AU  - Marković, Bojana
AU  - Sandić, Zvjezdana
AU  - Onjia, Antonije
AU  - Janjić, Goran
PY  - 2021
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/7037
AB  - Statistička analiza podataka dobijenih iz kristalnih struktura, ekstrahovanih iz Kembričke baze
strukturnih podataka (eng. CSD), pokazala je da atomi S i Se u nepolarnom okruženju pokazuju
sličnu tendenciju ka pojedinim tipovima interakcija [1]. Najbrojnije su strukture sa C-H…S i CH…Se interakcijama (~ 80%), dok su Se…Se i S …S interakcije druge po zastupljenosti (~ 5%).
Kada se S ili Se nalaze u polarnom okruženju (u neposrednoj blizini imaju O-H ili N-H grupu)
raspodela pojedinih tipova interakcija je nešto drugačija. Statistička analiza interakcija S i Se
(kriterijumi: d < 4.0Å (za S) d < 4.5Å (za Se), Slika) pokazala je da su najbrojnije interakcije sa H
atomom (u oba slučaja oko 47%), dok su interakcije koje uključuju C atome (interakcije sa
nepolarnim grupama) druge po zastupljenosti. Interakcije sa nepolarnim C-H grupama su nešto
zastupljenije kod Se (30%) nego kod S atoma (21%), dok su interakcije sa polarnim O-H i N-H
grupama manje brojne kod Se (ukupno 10%) nego kod S atoma (ukupno 16%). Neočekivano,
simultane interakcije X atoma sa S/Se atomom i polarnom O-H/N-H grupom (H…X<3.5 Å) su
zastupljene u udelu od samo 20% (Slika).
Rezultati doking studije sugerišu da bi PBISe (Se jedinjenje) moglo biti bolji inhibitor iNOS
(inducibilne azot-monoksid sintaze) nego njegov S derivat (PBIT). Sve orijentacije PBISe su
grupisane na istom mestu (aktivno mesto, Slika) što dovodi do mnogo bolje efikasnosti ovog
molekula u odnosu na PBIT, za kojeg su nađena tri mesta vezivanja (Slika). Ovo se slaže sa
eksperimentalnim rezultatima koji ukazuju na to da PBISe ubija ćelije melanoma više od 10 puta
efikasnije od drugog iNOS inhibitora (PBIT).
AB  - Statistical analysis of data from crystal structures, extracted from Cambridge Structural Database(CSD) have shown that S and Se atoms in nonpolar environment display similar tendencytoward specified type interactions [1]. The most numerous are structures with C−H···Se andC−H···S interactions (~80%), while structures with Se···Se and S···S interactions (~5%) are notablyless numerous (second type of interactions). When S or Se atoms is in a polar environment(there is OH or NH grous in the vicinity), the distribution of certain types of interactions is slightlydifferent. Statistical analysis of S and Se interactions (criteria: d < 4.0 Å (for S) d < 4.5 Å (for Se),Figure) showed the most numerous interactions with the H atom (in both cases about 47%), whileinteractions involving C atoms (interactions with non-polar groups) are second in prevalence.Interactions with non-polar C-H groups are slightly more numerous for Se (30%) than for S atom(21%), while interactions with polar O-H and N-H groups are less numerous for Se (10% in total)than in case of S atom (16% in total). Unexpectedly, the simultaneous interactions of X atom withthe S/Se atom and the polar OH/N-H group (H…X<3.5 Å) are only present in an amount of about20%.Results from docking study suggested that PBISe (Se compound) could be beter inhibitor ofiNOS (inducible nitric oxide synthase) than its S derivative (PBIT). All orientations of PBISe areclustered at the same site (active site, Figure) leading to much better efficiency of this moleculecompared to PBIT, where three binding sites can be observed (Figure). This is in strong agreementwith experimental results pointing that PBISe kills melanoma cells >10−fold more effectively thanother iNOS inhibitors (PBIT).
PB  - Beograd : Srpsko kristalografsko društvo
C3  - Izvodi radova / XXVII konferencija Srpskog kristalografskog društva, Kragujevac, 2021
T1  - Zamena sumpora selenom. Efekat polarnih grupa iz okruženja
T1  - Substitution of sulfur by selenium. Effect of polar groups from the environmental
EP  - 45
SP  - 44
UR  - https://hdl.handle.net/21.15107/rcub_technorep_7037
ER  - 
@conference{
author = "Suručić, Ljiljana and Tadić, Tamara and Nastasović, Aleksandra and Marković, Bojana and Sandić, Zvjezdana and Onjia, Antonije and Janjić, Goran",
year = "2021",
abstract = "Statistička analiza podataka dobijenih iz kristalnih struktura, ekstrahovanih iz Kembričke baze
strukturnih podataka (eng. CSD), pokazala je da atomi S i Se u nepolarnom okruženju pokazuju
sličnu tendenciju ka pojedinim tipovima interakcija [1]. Najbrojnije su strukture sa C-H…S i CH…Se interakcijama (~ 80%), dok su Se…Se i S …S interakcije druge po zastupljenosti (~ 5%).
Kada se S ili Se nalaze u polarnom okruženju (u neposrednoj blizini imaju O-H ili N-H grupu)
raspodela pojedinih tipova interakcija je nešto drugačija. Statistička analiza interakcija S i Se
(kriterijumi: d < 4.0Å (za S) d < 4.5Å (za Se), Slika) pokazala je da su najbrojnije interakcije sa H
atomom (u oba slučaja oko 47%), dok su interakcije koje uključuju C atome (interakcije sa
nepolarnim grupama) druge po zastupljenosti. Interakcije sa nepolarnim C-H grupama su nešto
zastupljenije kod Se (30%) nego kod S atoma (21%), dok su interakcije sa polarnim O-H i N-H
grupama manje brojne kod Se (ukupno 10%) nego kod S atoma (ukupno 16%). Neočekivano,
simultane interakcije X atoma sa S/Se atomom i polarnom O-H/N-H grupom (H…X<3.5 Å) su
zastupljene u udelu od samo 20% (Slika).
Rezultati doking studije sugerišu da bi PBISe (Se jedinjenje) moglo biti bolji inhibitor iNOS
(inducibilne azot-monoksid sintaze) nego njegov S derivat (PBIT). Sve orijentacije PBISe su
grupisane na istom mestu (aktivno mesto, Slika) što dovodi do mnogo bolje efikasnosti ovog
molekula u odnosu na PBIT, za kojeg su nađena tri mesta vezivanja (Slika). Ovo se slaže sa
eksperimentalnim rezultatima koji ukazuju na to da PBISe ubija ćelije melanoma više od 10 puta
efikasnije od drugog iNOS inhibitora (PBIT)., Statistical analysis of data from crystal structures, extracted from Cambridge Structural Database(CSD) have shown that S and Se atoms in nonpolar environment display similar tendencytoward specified type interactions [1]. The most numerous are structures with C−H···Se andC−H···S interactions (~80%), while structures with Se···Se and S···S interactions (~5%) are notablyless numerous (second type of interactions). When S or Se atoms is in a polar environment(there is OH or NH grous in the vicinity), the distribution of certain types of interactions is slightlydifferent. Statistical analysis of S and Se interactions (criteria: d < 4.0 Å (for S) d < 4.5 Å (for Se),Figure) showed the most numerous interactions with the H atom (in both cases about 47%), whileinteractions involving C atoms (interactions with non-polar groups) are second in prevalence.Interactions with non-polar C-H groups are slightly more numerous for Se (30%) than for S atom(21%), while interactions with polar O-H and N-H groups are less numerous for Se (10% in total)than in case of S atom (16% in total). Unexpectedly, the simultaneous interactions of X atom withthe S/Se atom and the polar OH/N-H group (H…X<3.5 Å) are only present in an amount of about20%.Results from docking study suggested that PBISe (Se compound) could be beter inhibitor ofiNOS (inducible nitric oxide synthase) than its S derivative (PBIT). All orientations of PBISe areclustered at the same site (active site, Figure) leading to much better efficiency of this moleculecompared to PBIT, where three binding sites can be observed (Figure). This is in strong agreementwith experimental results pointing that PBISe kills melanoma cells >10−fold more effectively thanother iNOS inhibitors (PBIT).",
publisher = "Beograd : Srpsko kristalografsko društvo",
journal = "Izvodi radova / XXVII konferencija Srpskog kristalografskog društva, Kragujevac, 2021",
title = "Zamena sumpora selenom. Efekat polarnih grupa iz okruženja, Substitution of sulfur by selenium. Effect of polar groups from the environmental",
pages = "45-44",
url = "https://hdl.handle.net/21.15107/rcub_technorep_7037"
}
Suručić, L., Tadić, T., Nastasović, A., Marković, B., Sandić, Z., Onjia, A.,& Janjić, G.. (2021). Zamena sumpora selenom. Efekat polarnih grupa iz okruženja. in Izvodi radova / XXVII konferencija Srpskog kristalografskog društva, Kragujevac, 2021
Beograd : Srpsko kristalografsko društvo., 44-45.
https://hdl.handle.net/21.15107/rcub_technorep_7037
Suručić L, Tadić T, Nastasović A, Marković B, Sandić Z, Onjia A, Janjić G. Zamena sumpora selenom. Efekat polarnih grupa iz okruženja. in Izvodi radova / XXVII konferencija Srpskog kristalografskog društva, Kragujevac, 2021. 2021;:44-45.
https://hdl.handle.net/21.15107/rcub_technorep_7037 .
Suručić, Ljiljana, Tadić, Tamara, Nastasović, Aleksandra, Marković, Bojana, Sandić, Zvjezdana, Onjia, Antonije, Janjić, Goran, "Zamena sumpora selenom. Efekat polarnih grupa iz okruženja" in Izvodi radova / XXVII konferencija Srpskog kristalografskog društva, Kragujevac, 2021 (2021):44-45,
https://hdl.handle.net/21.15107/rcub_technorep_7037 .

ULOGA MEĐUMOLEKULSKIH INTERAKCIJA U KRISTALNOM PAKOVANjU 3-IZOPROPIL I 3-CIKLOPROPIL DERIVATA FENITOINA

Trišović, Nemanja; Radovanović, Lidija; Janjić, Goran V.; Jelić, Stefan T.; Rogan, Jelena

(Beograd : Srpsko kristalografsko društvo, 2019)

TY  - CONF
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/123456789/6706
AB  - Sintetisana su dva derivata fenitoina (5,5-difenilhidantoina) i određene su
njihove kristalne strukture. Urađena je kvantitativna analiza kristalnog
pakovanja sa aspekta međumolekulskih interakcija i strukturnih motiva.
Kristalno pakovanje 3-izopropil-5,5-difenilhidantoina sadrži
centrosimetrične dimere povezane parom N–H∙∙∙O vodoničnih veza koji se dalje
umrežavaju pomoću C–H∙∙∙O interakcija i paralelnih interakcija između fenilnih
prstenova na velikom rastojanju u lance paralelne s-osi (slika 1). Osnovna
karakteristika kristalne strukture 3-ciklopropil-5,5-difenilhidantoina jesu
lanci koji nastaju preko N–H∙∙∙O vodoničnih veza, C–H∙∙∙O i C–H∙∙∙π interakcija
(slika 2). Predstavljeno istraživanje daje uvid u ulogu međumolekulskih interakcija u
kristalnom pakovanju proučavanih jedinjenja, kao i dalje smernice za dizajniranje
novih derivata fenitoina sa poboljšanim farmaceutskim svojstvima. Strukturni podaci 3-izopropil-5,5-difenilhidantoina: C18H18N2O2,
trikliničan sistem, prostorna grupa P–1, a = 8,5357(9), b = 8,6225(8),
c = 12,3979(9) Å, α = 104,010(7), β = 91,826(7), γ = 115,201(10) °, V = 791,54(14) Å3
,
R1 = 0,0473.
Strukturni podaci3-ciklopropil-5,5-difenilhidantoina: C18H16N2O2,
monokliničan sistem, prostorna grupa P21/c, a = 11,5996(5), b = 10,6459(3),
c = 12,2992(5) Å, β = 101,977(4) °, V = 1485,74(10) Å3
, R1 = 0,0403.
AB  - Two derivatives of phenytoin (5,5-diphenylhydantoin) were synthesized and their crystal
structures were determined. The quantitative analysis of the crystal packings in terms of the
contributing intermolecular interactions and structural motifs has been done. The crystal packing of 3-isopropyl-5,5-diphenylhydantoin contains centrosymmetric dimers linked by paired
N–H∙∙∙O hydrogen bonds which further self-organize through pairs of C–H∙∙∙O interactions and
a parallel interaction of two phenyl rings at a large offset into chains running along the c-axis
(Figure 1). The principal feature of the crystal structure of 3-cyclopropyl-5,5-
diphenylhydantoin is formation of the chains by N–H∙∙∙O hydrogen bonds, C–H∙∙∙O and C–
H∙∙∙π interactions (Figure 2). The presented investigation provide not only new insight into the
role of intermolecular interactions in the crystal packing, but also guidance for furthering
crystal engineering to design novel hydantoin derivatives with improved pharmaceutical
properties. Crystal data for 3-isopropyl-5,5-diphenylhydantoin: C18H18N2O2, triclinic, P–1,
a = 8.5357(9), b = 8.6225(8), c = 12.3979(9) Å, α = 104.010(7), β = 91.826(7),
γ = 115.201(10) °, V = 791.54(14) Å3
, R1 = 0.0473.
Crystal data for 3-cyclopropyl-5,5-diphenylhydantoin: C18H16N2O2, monoclinic, P21/c,
a = 11.5996(5), b = 10.6459(3), c = 12.2992(5) Å, β = 101.977(4) °, V = 1485.74(10) Å3
,
R1 = 0.0403.
PB  - Beograd : Srpsko kristalografsko društvo
C3  - Izvodi radova / XXVI konferencija Srpskog kristalografskog društva, Srebrno jezero, 27–28. jun 2019
T1  - ULOGA MEĐUMOLEKULSKIH INTERAKCIJA U KRISTALNOM PAKOVANjU 3-IZOPROPIL I 3-CIKLOPROPIL DERIVATA FENITOINA
T1  - THE ROLE OF INTERMOLECULAR INTERACTIONS IN THE CRYSTAL PACKING OF 3-ISOPROPYL AND 3-CYCLOPROPYL DERIVATIVES OF PHENYTOIN
EP  - 31
SP  - 30
UR  - https://hdl.handle.net/21.15107/rcub_technorep_6706
ER  - 
@conference{
author = "Trišović, Nemanja and Radovanović, Lidija and Janjić, Goran V. and Jelić, Stefan T. and Rogan, Jelena",
year = "2019",
abstract = "Sintetisana su dva derivata fenitoina (5,5-difenilhidantoina) i određene su
njihove kristalne strukture. Urađena je kvantitativna analiza kristalnog
pakovanja sa aspekta međumolekulskih interakcija i strukturnih motiva.
Kristalno pakovanje 3-izopropil-5,5-difenilhidantoina sadrži
centrosimetrične dimere povezane parom N–H∙∙∙O vodoničnih veza koji se dalje
umrežavaju pomoću C–H∙∙∙O interakcija i paralelnih interakcija između fenilnih
prstenova na velikom rastojanju u lance paralelne s-osi (slika 1). Osnovna
karakteristika kristalne strukture 3-ciklopropil-5,5-difenilhidantoina jesu
lanci koji nastaju preko N–H∙∙∙O vodoničnih veza, C–H∙∙∙O i C–H∙∙∙π interakcija
(slika 2). Predstavljeno istraživanje daje uvid u ulogu međumolekulskih interakcija u
kristalnom pakovanju proučavanih jedinjenja, kao i dalje smernice za dizajniranje
novih derivata fenitoina sa poboljšanim farmaceutskim svojstvima. Strukturni podaci 3-izopropil-5,5-difenilhidantoina: C18H18N2O2,
trikliničan sistem, prostorna grupa P–1, a = 8,5357(9), b = 8,6225(8),
c = 12,3979(9) Å, α = 104,010(7), β = 91,826(7), γ = 115,201(10) °, V = 791,54(14) Å3
,
R1 = 0,0473.
Strukturni podaci3-ciklopropil-5,5-difenilhidantoina: C18H16N2O2,
monokliničan sistem, prostorna grupa P21/c, a = 11,5996(5), b = 10,6459(3),
c = 12,2992(5) Å, β = 101,977(4) °, V = 1485,74(10) Å3
, R1 = 0,0403., Two derivatives of phenytoin (5,5-diphenylhydantoin) were synthesized and their crystal
structures were determined. The quantitative analysis of the crystal packings in terms of the
contributing intermolecular interactions and structural motifs has been done. The crystal packing of 3-isopropyl-5,5-diphenylhydantoin contains centrosymmetric dimers linked by paired
N–H∙∙∙O hydrogen bonds which further self-organize through pairs of C–H∙∙∙O interactions and
a parallel interaction of two phenyl rings at a large offset into chains running along the c-axis
(Figure 1). The principal feature of the crystal structure of 3-cyclopropyl-5,5-
diphenylhydantoin is formation of the chains by N–H∙∙∙O hydrogen bonds, C–H∙∙∙O and C–
H∙∙∙π interactions (Figure 2). The presented investigation provide not only new insight into the
role of intermolecular interactions in the crystal packing, but also guidance for furthering
crystal engineering to design novel hydantoin derivatives with improved pharmaceutical
properties. Crystal data for 3-isopropyl-5,5-diphenylhydantoin: C18H18N2O2, triclinic, P–1,
a = 8.5357(9), b = 8.6225(8), c = 12.3979(9) Å, α = 104.010(7), β = 91.826(7),
γ = 115.201(10) °, V = 791.54(14) Å3
, R1 = 0.0473.
Crystal data for 3-cyclopropyl-5,5-diphenylhydantoin: C18H16N2O2, monoclinic, P21/c,
a = 11.5996(5), b = 10.6459(3), c = 12.2992(5) Å, β = 101.977(4) °, V = 1485.74(10) Å3
,
R1 = 0.0403.",
publisher = "Beograd : Srpsko kristalografsko društvo",
journal = "Izvodi radova / XXVI konferencija Srpskog kristalografskog društva, Srebrno jezero, 27–28. jun 2019",
title = "ULOGA MEĐUMOLEKULSKIH INTERAKCIJA U KRISTALNOM PAKOVANjU 3-IZOPROPIL I 3-CIKLOPROPIL DERIVATA FENITOINA, THE ROLE OF INTERMOLECULAR INTERACTIONS IN THE CRYSTAL PACKING OF 3-ISOPROPYL AND 3-CYCLOPROPYL DERIVATIVES OF PHENYTOIN",
pages = "31-30",
url = "https://hdl.handle.net/21.15107/rcub_technorep_6706"
}
Trišović, N., Radovanović, L., Janjić, G. V., Jelić, S. T.,& Rogan, J.. (2019). ULOGA MEĐUMOLEKULSKIH INTERAKCIJA U KRISTALNOM PAKOVANjU 3-IZOPROPIL I 3-CIKLOPROPIL DERIVATA FENITOINA. in Izvodi radova / XXVI konferencija Srpskog kristalografskog društva, Srebrno jezero, 27–28. jun 2019
Beograd : Srpsko kristalografsko društvo., 30-31.
https://hdl.handle.net/21.15107/rcub_technorep_6706
Trišović N, Radovanović L, Janjić GV, Jelić ST, Rogan J. ULOGA MEĐUMOLEKULSKIH INTERAKCIJA U KRISTALNOM PAKOVANjU 3-IZOPROPIL I 3-CIKLOPROPIL DERIVATA FENITOINA. in Izvodi radova / XXVI konferencija Srpskog kristalografskog društva, Srebrno jezero, 27–28. jun 2019. 2019;:30-31.
https://hdl.handle.net/21.15107/rcub_technorep_6706 .
Trišović, Nemanja, Radovanović, Lidija, Janjić, Goran V., Jelić, Stefan T., Rogan, Jelena, "ULOGA MEĐUMOLEKULSKIH INTERAKCIJA U KRISTALNOM PAKOVANjU 3-IZOPROPIL I 3-CIKLOPROPIL DERIVATA FENITOINA" in Izvodi radova / XXVI konferencija Srpskog kristalografskog društva, Srebrno jezero, 27–28. jun 2019 (2019):30-31,
https://hdl.handle.net/21.15107/rcub_technorep_6706 .