TY  - JOUR
AU  - Rajić, Nevenka
AU  - Stojaković, Djordje
PY  - 1996
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6398
AB  - High field magic-angle spinning (MAS) (31)P-NMR investigations of novel porous zincophosphates and their cobalt-containing derivatives confirm the framework structure of alternating Zn(Co)O4 and PO4 tetrahedra. The MAS NMR spectrum of cobalt-containing products exhibits a large anisotropy manifested in numerous side bands. This effect is attributed to paramagnetic shifts induced by dipolar interactions between the unpaired electrons of Co(2+) and the (31)P nuclei. The relative intensity of the side bands is significantly lower in the cobalt-exchanged sample (where the Co(2+) does not occupa framework sites) than direct evidence of extra-framework cobalt(II) or of Co(II)  incorporation in the zincophosphate lattice.
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - (31)P NMR investigation of some microporous zincophosphates
EP  - 111
IS  - 2
SP  - 107
VL  - 61
UR  - https://hdl.handle.net/21.15107/rcub_technorep_6398
ER  - 

@article{
author = "Rajić, Nevenka and Stojaković, Djordje",
year = "1996",
abstract = "High field magic-angle spinning (MAS) (31)P-NMR investigations of novel porous zincophosphates and their cobalt-containing derivatives confirm the framework structure of alternating Zn(Co)O4 and PO4 tetrahedra. The MAS NMR spectrum of cobalt-containing products exhibits a large anisotropy manifested in numerous side bands. This effect is attributed to paramagnetic shifts induced by dipolar interactions between the unpaired electrons of Co(2+) and the (31)P nuclei. The relative intensity of the side bands is significantly lower in the cobalt-exchanged sample (where the Co(2+) does not occupa framework sites) than direct evidence of extra-framework cobalt(II) or of Co(II)  incorporation in the zincophosphate lattice.",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "(31)P NMR investigation of some microporous zincophosphates",
pages = "111-107",
number = "2",
volume = "61",
url = "https://hdl.handle.net/21.15107/rcub_technorep_6398"
}

Rajić, N.,& Stojaković, D.. (1996). (31)P NMR investigation of some microporous zincophosphates. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 61(2), 107-111.
https://hdl.handle.net/21.15107/rcub_technorep_6398

Rajić N, Stojaković D. (31)P NMR investigation of some microporous zincophosphates. in Journal of the Serbian Chemical Society. 1996;61(2):107-111.
https://hdl.handle.net/21.15107/rcub_technorep_6398 .

Rajić, Nevenka, Stojaković, Djordje, "(31)P NMR investigation of some microporous zincophosphates" in Journal of the Serbian Chemical Society, 61, no. 2 (1996):107-111,
https://hdl.handle.net/21.15107/rcub_technorep_6398 .

TY  - JOUR
AU  - Stojaković, Djordje
AU  - Rajić, Nevenka
PY  - 1996
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5213
AB  - A model system structurally based on CoAPO-21 has been studied by the PM3 MO method in order to examine the conformation of the encapsulated template species. It is confirmed that the observed conformation of the template ethylenediammonium ion in the framework  cavities corresponds to the energy minimum for the system. The spatial position of the hydrogen atoms of the template has also been estimated. The geometry of the ion should be primarily attributed to steric factors. Intra-molecular hydrogen bonding between template and the aluminophosphate lattice occurs through the N-H...O bonds that vary in strength due to steric reasons.
PB  - Akadémiai Kiadó
T2  - ACH Models in Chemistry
T1  - A study of the template conformation in CoAPO-21
EP  - 339
IS  - 4
SP  - 333
VL  - 133
UR  - https://hdl.handle.net/21.15107/rcub_technorep_5213
ER  - 

@article{
author = "Stojaković, Djordje and Rajić, Nevenka",
year = "1996",
abstract = "A model system structurally based on CoAPO-21 has been studied by the PM3 MO method in order to examine the conformation of the encapsulated template species. It is confirmed that the observed conformation of the template ethylenediammonium ion in the framework  cavities corresponds to the energy minimum for the system. The spatial position of the hydrogen atoms of the template has also been estimated. The geometry of the ion should be primarily attributed to steric factors. Intra-molecular hydrogen bonding between template and the aluminophosphate lattice occurs through the N-H...O bonds that vary in strength due to steric reasons.",
publisher = "Akadémiai Kiadó",
journal = "ACH Models in Chemistry",
title = "A study of the template conformation in CoAPO-21",
pages = "339-333",
number = "4",
volume = "133",
url = "https://hdl.handle.net/21.15107/rcub_technorep_5213"
}

Stojaković, D.,& Rajić, N.. (1996). A study of the template conformation in CoAPO-21. in ACH Models in Chemistry
Akadémiai Kiadó., 133(4), 333-339.
https://hdl.handle.net/21.15107/rcub_technorep_5213

Stojaković D, Rajić N. A study of the template conformation in CoAPO-21. in ACH Models in Chemistry. 1996;133(4):333-339.
https://hdl.handle.net/21.15107/rcub_technorep_5213 .

Stojaković, Djordje, Rajić, Nevenka, "A study of the template conformation in CoAPO-21" in ACH Models in Chemistry, 133, no. 4 (1996):333-339,
https://hdl.handle.net/21.15107/rcub_technorep_5213 .

TY  - JOUR
AU  - Stojaković, Djordje
AU  - Rajić, Nevenka
PY  - 1995
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5158
AB  - The coordination geometry and electronic structure of the NiX4(2-) complex ions (X=Cl, Br, I) have been studied by the Fenske-Hall SCF method. The calculation confirm the presence of tetrahedral over square-planar geometry. They also show that the MO energy level splitting is consistent with the spectrochemical series. The calculation confirm that the Ni-X bond becomes increasingly covalent in the series: NiCl4(2-), NiBr4(2-), NiI4(2-)
PB  - Society of Chemists and Technologists of Macedonia
T2  - Bulletin of the Chemists and Technologists of Macedonia
T1  - A study of the tetrahallogenonickel(II) complexes by the Fenske-Hall molecular orbital method
EP  - 100
IS  - 2
SP  - 95
VL  - 14
UR  - https://hdl.handle.net/21.15107/rcub_technorep_5158
ER  - 

@article{
author = "Stojaković, Djordje and Rajić, Nevenka",
year = "1995",
abstract = "The coordination geometry and electronic structure of the NiX4(2-) complex ions (X=Cl, Br, I) have been studied by the Fenske-Hall SCF method. The calculation confirm the presence of tetrahedral over square-planar geometry. They also show that the MO energy level splitting is consistent with the spectrochemical series. The calculation confirm that the Ni-X bond becomes increasingly covalent in the series: NiCl4(2-), NiBr4(2-), NiI4(2-)",
publisher = "Society of Chemists and Technologists of Macedonia",
journal = "Bulletin of the Chemists and Technologists of Macedonia",
title = "A study of the tetrahallogenonickel(II) complexes by the Fenske-Hall molecular orbital method",
pages = "100-95",
number = "2",
volume = "14",
url = "https://hdl.handle.net/21.15107/rcub_technorep_5158"
}

Stojaković, D.,& Rajić, N.. (1995). A study of the tetrahallogenonickel(II) complexes by the Fenske-Hall molecular orbital method. in Bulletin of the Chemists and Technologists of Macedonia
Society of Chemists and Technologists of Macedonia., 14(2), 95-100.
https://hdl.handle.net/21.15107/rcub_technorep_5158

Stojaković D, Rajić N. A study of the tetrahallogenonickel(II) complexes by the Fenske-Hall molecular orbital method. in Bulletin of the Chemists and Technologists of Macedonia. 1995;14(2):95-100.
https://hdl.handle.net/21.15107/rcub_technorep_5158 .

Stojaković, Djordje, Rajić, Nevenka, "A study of the tetrahallogenonickel(II) complexes by the Fenske-Hall molecular orbital method" in Bulletin of the Chemists and Technologists of Macedonia, 14, no. 2 (1995):95-100,
https://hdl.handle.net/21.15107/rcub_technorep_5158 .

TY  - JOUR
AU  - Stojaković, Đorđe
AU  - Rajić, Nevenka
PY  - 1994
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6395
AB  - The reaction of a 1:3 molar mixture of the monosodium salt of 4-sulfophthalic acid and phthalic acod, carried out in the presence of NH4Cl, urea, CuSO4 5H2O, and (NH4)2MoO4, does not yield the mono-substituted derivative, i.e., the sodium salt of copper-phthalocyanine-4-sulfonic acid (mSCuPc) but a 1:3 mixture of tetrasodium salt of copper-phthalocyanine-4-sulfonic acid-4,4',4'',4'''-tetrasulfonic acid (tSCuPc) and copper phthalocyanine (CuPc). However, quantum-mechanical calculations indicate that mSCuPc should be energetically favoured over the equivalent mixture of tSCuPc and CuPc. The preferential formation of the latter mixture has been attributed to kinetic factors arising from simultaneous presence of ionic and covalent species in the reaction medium.
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - On the possibility of the direct preparation of the sodium salt of copper phthalocyanine-4-sulfonic acid
EP  - 561
SP  - 557
UR  - https://hdl.handle.net/21.15107/rcub_technorep_6395
ER  - 

@article{
author = "Stojaković, Đorđe and Rajić, Nevenka",
year = "1994",
abstract = "The reaction of a 1:3 molar mixture of the monosodium salt of 4-sulfophthalic acid and phthalic acod, carried out in the presence of NH4Cl, urea, CuSO4 5H2O, and (NH4)2MoO4, does not yield the mono-substituted derivative, i.e., the sodium salt of copper-phthalocyanine-4-sulfonic acid (mSCuPc) but a 1:3 mixture of tetrasodium salt of copper-phthalocyanine-4-sulfonic acid-4,4',4'',4'''-tetrasulfonic acid (tSCuPc) and copper phthalocyanine (CuPc). However, quantum-mechanical calculations indicate that mSCuPc should be energetically favoured over the equivalent mixture of tSCuPc and CuPc. The preferential formation of the latter mixture has been attributed to kinetic factors arising from simultaneous presence of ionic and covalent species in the reaction medium.",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "On the possibility of the direct preparation of the sodium salt of copper phthalocyanine-4-sulfonic acid",
pages = "561-557",
url = "https://hdl.handle.net/21.15107/rcub_technorep_6395"
}

Stojaković, Đ.,& Rajić, N.. (1994). On the possibility of the direct preparation of the sodium salt of copper phthalocyanine-4-sulfonic acid. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 557-561.
https://hdl.handle.net/21.15107/rcub_technorep_6395

Stojaković Đ, Rajić N. On the possibility of the direct preparation of the sodium salt of copper phthalocyanine-4-sulfonic acid. in Journal of the Serbian Chemical Society. 1994;:557-561.
https://hdl.handle.net/21.15107/rcub_technorep_6395 .

Stojaković, Đorđe, Rajić, Nevenka, "On the possibility of the direct preparation of the sodium salt of copper phthalocyanine-4-sulfonic acid" in Journal of the Serbian Chemical Society (1994):557-561,
https://hdl.handle.net/21.15107/rcub_technorep_6395 .

TY  - JOUR
AU  - Stojaković, Djordje
AU  - Rajić, Nevenka
PY  - 1993
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6394
AB  - A convenient method for copper analysis in copper phthalocyanine and its ring-substituted derivates has been studied. It is based on the complete destruction of the organic component in the sample by a combination of thermal decomposition and oxidation in air, and a treatment with aqua regia. The procedure results in the solubilization of entire copper content.
T2  - Journal of the Serbian Chemical Society
T1  - On the determination of copper in its phthalocyanine complex
EP  - 704
SP  - 701
UR  - https://hdl.handle.net/21.15107/rcub_technorep_6394
ER  - 

@article{
author = "Stojaković, Djordje and Rajić, Nevenka",
year = "1993",
abstract = "A convenient method for copper analysis in copper phthalocyanine and its ring-substituted derivates has been studied. It is based on the complete destruction of the organic component in the sample by a combination of thermal decomposition and oxidation in air, and a treatment with aqua regia. The procedure results in the solubilization of entire copper content.",
journal = "Journal of the Serbian Chemical Society",
title = "On the determination of copper in its phthalocyanine complex",
pages = "704-701",
url = "https://hdl.handle.net/21.15107/rcub_technorep_6394"
}

Stojaković, D.,& Rajić, N.. (1993). On the determination of copper in its phthalocyanine complex. in Journal of the Serbian Chemical Society, 701-704.
https://hdl.handle.net/21.15107/rcub_technorep_6394

Stojaković D, Rajić N. On the determination of copper in its phthalocyanine complex. in Journal of the Serbian Chemical Society. 1993;:701-704.
https://hdl.handle.net/21.15107/rcub_technorep_6394 .

Stojaković, Djordje, Rajić, Nevenka, "On the determination of copper in its phthalocyanine complex" in Journal of the Serbian Chemical Society (1993):701-704,
https://hdl.handle.net/21.15107/rcub_technorep_6394 .

TY  - JOUR
AU  - Rajić, Nevenka
AU  - Stojaković, Djordje
AU  - Hočevar, Stanko
AU  - Kaučič, Venčeslav
PY  - 1993
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5053
AB  - Hydrothermal synthesis of SAPO materials using isopropylamine (i-PrNH2) as the template leads to the formation of MnAPSO-34 if Mn(II) is present. In the presence of Cr(III), the synthesis yields SAPO-34 containing chromium(III), which is not incorporated in the silicoaluminophosphate lattice. Calcination of MnAPSO-34 results in oxidation of Mn(II); the calcinated product can be subsequently reduced back to MnAPSO-34. The MnAPSO-34 material catalyzes dehydration of methanol, and its catalytic activity is higher than that of SAPO-34.
PB  - Butterworth-Heinemann
T2  - ZEOLITES
T1  - On the possibility of incorporating Mn(II) and Cr(III) in SAPO-34 in the presence of isopropylamine as a template
EP  - 387
IS  - 5
SP  - 384
VL  - 13
DO  - 10.1016/0144-2449(93)90154-U
ER  - 

@article{
author = "Rajić, Nevenka and Stojaković, Djordje and Hočevar, Stanko and Kaučič, Venčeslav",
year = "1993",
abstract = "Hydrothermal synthesis of SAPO materials using isopropylamine (i-PrNH2) as the template leads to the formation of MnAPSO-34 if Mn(II) is present. In the presence of Cr(III), the synthesis yields SAPO-34 containing chromium(III), which is not incorporated in the silicoaluminophosphate lattice. Calcination of MnAPSO-34 results in oxidation of Mn(II); the calcinated product can be subsequently reduced back to MnAPSO-34. The MnAPSO-34 material catalyzes dehydration of methanol, and its catalytic activity is higher than that of SAPO-34.",
publisher = "Butterworth-Heinemann",
journal = "ZEOLITES",
title = "On the possibility of incorporating Mn(II) and Cr(III) in SAPO-34 in the presence of isopropylamine as a template",
pages = "387-384",
number = "5",
volume = "13",
doi = "10.1016/0144-2449(93)90154-U"
}

Rajić, N., Stojaković, D., Hočevar, S.,& Kaučič, V.. (1993). On the possibility of incorporating Mn(II) and Cr(III) in SAPO-34 in the presence of isopropylamine as a template. in ZEOLITES
Butterworth-Heinemann., 13(5), 384-387.
https://doi.org/10.1016/0144-2449(93)90154-U

Rajić N, Stojaković D, Hočevar S, Kaučič V. On the possibility of incorporating Mn(II) and Cr(III) in SAPO-34 in the presence of isopropylamine as a template. in ZEOLITES. 1993;13(5):384-387.
doi:10.1016/0144-2449(93)90154-U .

Rajić, Nevenka, Stojaković, Djordje, Hočevar, Stanko, Kaučič, Venčeslav, "On the possibility of incorporating Mn(II) and Cr(III) in SAPO-34 in the presence of isopropylamine as a template" in ZEOLITES, 13, no. 5 (1993):384-387,
https://doi.org/10.1016/0144-2449(93)90154-U . .

TY  - JOUR
AU  - Batista, Jurka
AU  - Kaučič, Venčeslav
AU  - Rajić, Nevenka
AU  - Stojaković, Djordje
PY  - 1992
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5054
AB  - Hydrothermal synthesis of CoAPSO-44 in the presence of cyclohexylamine (CHA) as the template is generally accompanied by the formation of an unknown phase, “Co(APSO)N.” Electronic spectroscopy indicates that CO(APSO)N contains Co2+ in a pentacoordinated environment. When Co(APSO)N is heated at 195°C in a water suspension under autogenic pressure, two processes occur: (a) a partial conversion of Co(APSO)N into CoAPSO-44 and (b) decomposition of Co(APSO)N into Co- and Al-phosphates. Thermal removal of CHA from Co(APSO)N results in a breakdown of the latter's cyrstal lattice.
PB  - Butterworth-Heinemann
T2  - ZEOLITES
T1  - On the formation of CoAPSO-44
EP  - 928
IS  - 8
SP  - 925
VL  - 12
DO  - 10.1016/0144-2449(92)90156-J
ER  - 

@article{
author = "Batista, Jurka and Kaučič, Venčeslav and Rajić, Nevenka and Stojaković, Djordje",
year = "1992",
abstract = "Hydrothermal synthesis of CoAPSO-44 in the presence of cyclohexylamine (CHA) as the template is generally accompanied by the formation of an unknown phase, “Co(APSO)N.” Electronic spectroscopy indicates that CO(APSO)N contains Co2+ in a pentacoordinated environment. When Co(APSO)N is heated at 195°C in a water suspension under autogenic pressure, two processes occur: (a) a partial conversion of Co(APSO)N into CoAPSO-44 and (b) decomposition of Co(APSO)N into Co- and Al-phosphates. Thermal removal of CHA from Co(APSO)N results in a breakdown of the latter's cyrstal lattice.",
publisher = "Butterworth-Heinemann",
journal = "ZEOLITES",
title = "On the formation of CoAPSO-44",
pages = "928-925",
number = "8",
volume = "12",
doi = "10.1016/0144-2449(92)90156-J"
}

Batista, J., Kaučič, V., Rajić, N.,& Stojaković, D.. (1992). On the formation of CoAPSO-44. in ZEOLITES
Butterworth-Heinemann., 12(8), 925-928.
https://doi.org/10.1016/0144-2449(92)90156-J

Batista J, Kaučič V, Rajić N, Stojaković D. On the formation of CoAPSO-44. in ZEOLITES. 1992;12(8):925-928.
doi:10.1016/0144-2449(92)90156-J .

Batista, Jurka, Kaučič, Venčeslav, Rajić, Nevenka, Stojaković, Djordje, "On the formation of CoAPSO-44" in ZEOLITES, 12, no. 8 (1992):925-928,
https://doi.org/10.1016/0144-2449(92)90156-J . .

TY  - JOUR
AU  - Rajić, Nevenka
AU  - Stojaković, Djordje
AU  - Kaučič, Venčeslav
PY  - 1991
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5062
AB  - Nickel(ll)-substituted aluminophosphates of structure types 21 and 12 (NiAPO-21 and NiAPO-12) have been prepared hydrothermally in the presence of ethylenediamine as the template. U.v.-visible spectroscopy of NiAPO-21 suggests that Ni(ll) replaces hexacoordinated aluminum of the AIP04-21 framework and is octahedrally coordinated by the 0 atoms of the aluminophosphate skeleton and also by H20 and en molecules. It has also been found that in the presence of copper no aluminophosphate-type products can be obtained.
PB  - Butterworth-Heinemann
T2  - Zeolites
T1  - Preparation of aluminophosphate  molecular sieves in the presence of  nickel( II) and copper( II)
EP  - 616
IS  - 6
SP  - 612
VL  - 11
DO  - 10.1016/S0144-2449(05)80013-2
ER  - 

@article{
author = "Rajić, Nevenka and Stojaković, Djordje and Kaučič, Venčeslav",
year = "1991",
abstract = "Nickel(ll)-substituted aluminophosphates of structure types 21 and 12 (NiAPO-21 and NiAPO-12) have been prepared hydrothermally in the presence of ethylenediamine as the template. U.v.-visible spectroscopy of NiAPO-21 suggests that Ni(ll) replaces hexacoordinated aluminum of the AIP04-21 framework and is octahedrally coordinated by the 0 atoms of the aluminophosphate skeleton and also by H20 and en molecules. It has also been found that in the presence of copper no aluminophosphate-type products can be obtained.",
publisher = "Butterworth-Heinemann",
journal = "Zeolites",
title = "Preparation of aluminophosphate  molecular sieves in the presence of  nickel( II) and copper( II)",
pages = "616-612",
number = "6",
volume = "11",
doi = "10.1016/S0144-2449(05)80013-2"
}

Rajić, N., Stojaković, D.,& Kaučič, V.. (1991). Preparation of aluminophosphate  molecular sieves in the presence of  nickel( II) and copper( II). in Zeolites
Butterworth-Heinemann., 11(6), 612-616.
https://doi.org/10.1016/S0144-2449(05)80013-2

Rajić N, Stojaković D, Kaučič V. Preparation of aluminophosphate  molecular sieves in the presence of  nickel( II) and copper( II). in Zeolites. 1991;11(6):612-616.
doi:10.1016/S0144-2449(05)80013-2 .

Rajić, Nevenka, Stojaković, Djordje, Kaučič, Venčeslav, "Preparation of aluminophosphate  molecular sieves in the presence of  nickel( II) and copper( II)" in Zeolites, 11, no. 6 (1991):612-616,
https://doi.org/10.1016/S0144-2449(05)80013-2 . .

TY  - JOUR
AU  - Rajić, Nevenka
AU  - Stojaković, Djordje
AU  - Kaučič, Venčeslav
PY  - 1991
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5056
AB  - The SAPO, MeAPO and MeSAPO microporous materials (Me=Co2+ and/or 2n2+) having a sodalite structure have been obtained hydrothermally at 200°C in the presence of tetramethylammonium ion as the template. The SAPO and MeSAPO products prepared at lower template concentrations are formed through a partial replacement of both aluminium and phosphorus by silicon in the parent aluminophosphate lattice; at higher pH only phosphorus is replaced. While the Me2+ ions are in all cases constituents of the framework, most zinc-containing materials have a fraction of the Zn2+ ions located in the cavities. T.g.a . shows that complete removal of the trapped organic component can not be easily accomplished. This can be explained by the small size of the openings in the sodalite cages. Powder diffraction analysis shows that replacement of aluminium by silicon, cobalt and zinc, and phosphorus by silicon leads to an expansion of the parent aluminophosphate unit cell. Kinetic studies suggest that crystallization of the silicon-containing products is preceded by an induction period of about 2 h, the nucleation taking place both in the liquid and solid phase.
PB  - CSIRO PUBLISHING
T2  - Australian Journal of Chemistry
T1  - Preparation and Properties of Sodalite-Type Aluminophosphates Containing Silicon, Cobalt and Zinc
EP  - 553
IS  - 4
SP  - 543
VL  - 44
DO  - 10.1071/CH9910543
ER  - 

@article{
author = "Rajić, Nevenka and Stojaković, Djordje and Kaučič, Venčeslav",
year = "1991",
abstract = "The SAPO, MeAPO and MeSAPO microporous materials (Me=Co2+ and/or 2n2+) having a sodalite structure have been obtained hydrothermally at 200°C in the presence of tetramethylammonium ion as the template. The SAPO and MeSAPO products prepared at lower template concentrations are formed through a partial replacement of both aluminium and phosphorus by silicon in the parent aluminophosphate lattice; at higher pH only phosphorus is replaced. While the Me2+ ions are in all cases constituents of the framework, most zinc-containing materials have a fraction of the Zn2+ ions located in the cavities. T.g.a . shows that complete removal of the trapped organic component can not be easily accomplished. This can be explained by the small size of the openings in the sodalite cages. Powder diffraction analysis shows that replacement of aluminium by silicon, cobalt and zinc, and phosphorus by silicon leads to an expansion of the parent aluminophosphate unit cell. Kinetic studies suggest that crystallization of the silicon-containing products is preceded by an induction period of about 2 h, the nucleation taking place both in the liquid and solid phase.",
publisher = "CSIRO PUBLISHING",
journal = "Australian Journal of Chemistry",
title = "Preparation and Properties of Sodalite-Type Aluminophosphates Containing Silicon, Cobalt and Zinc",
pages = "553-543",
number = "4",
volume = "44",
doi = "10.1071/CH9910543"
}

Rajić, N., Stojaković, D.,& Kaučič, V.. (1991). Preparation and Properties of Sodalite-Type Aluminophosphates Containing Silicon, Cobalt and Zinc. in Australian Journal of Chemistry
CSIRO PUBLISHING., 44(4), 543-553.
https://doi.org/10.1071/CH9910543

Rajić N, Stojaković D, Kaučič V. Preparation and Properties of Sodalite-Type Aluminophosphates Containing Silicon, Cobalt and Zinc. in Australian Journal of Chemistry. 1991;44(4):543-553.
doi:10.1071/CH9910543 .

Rajić, Nevenka, Stojaković, Djordje, Kaučič, Venčeslav, "Preparation and Properties of Sodalite-Type Aluminophosphates Containing Silicon, Cobalt and Zinc" in Australian Journal of Chemistry, 44, no. 4 (1991):543-553,
https://doi.org/10.1071/CH9910543 . .

TY  - JOUR
AU  - Rajić, Nevenka
AU  - Stojaković, Djordje
AU  - Kaučič, Venčeslav
PY  - 1990
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5060
AB  - Two materials, AIPO4-15 and CoAPO-15, with the same aluminophosphate lattice have been obtained by hydrothermal synthesis in the presence of hexamethylenetetramine (HMTA). Their formation is attributed to the influence of species that arise through the decomposition of HMTA, the latter process taking place under synthetic conditions. The Co 2+ ion in CoAPO-15 occupies tetragonally deformed octahedral sites, and this causes a slight expansion of the unit cell of CoAPO-15 in comparison to that of AIPO4-15. The Co 2+ ion is coordinated not only by the O atoms of the system but also by NH3 molecules.
PB  - Butterworth-Heinemann
T2  - Zeolites
T1  - Formation of AlPO4-15 and CoAPO-15 in the presence of hexamethylenetetramine
EP  - 805
IS  - 8
SP  - 802
VL  - 10
DO  - https://doi.org/10.1016/0144-2449(90)90066-Z
ER  - 

@article{
author = "Rajić, Nevenka and Stojaković, Djordje and Kaučič, Venčeslav",
year = "1990",
abstract = "Two materials, AIPO4-15 and CoAPO-15, with the same aluminophosphate lattice have been obtained by hydrothermal synthesis in the presence of hexamethylenetetramine (HMTA). Their formation is attributed to the influence of species that arise through the decomposition of HMTA, the latter process taking place under synthetic conditions. The Co 2+ ion in CoAPO-15 occupies tetragonally deformed octahedral sites, and this causes a slight expansion of the unit cell of CoAPO-15 in comparison to that of AIPO4-15. The Co 2+ ion is coordinated not only by the O atoms of the system but also by NH3 molecules.",
publisher = "Butterworth-Heinemann",
journal = "Zeolites",
title = "Formation of AlPO4-15 and CoAPO-15 in the presence of hexamethylenetetramine",
pages = "805-802",
number = "8",
volume = "10",
doi = "https://doi.org/10.1016/0144-2449(90)90066-Z"
}

Rajić, N., Stojaković, D.,& Kaučič, V.. (1990). Formation of AlPO4-15 and CoAPO-15 in the presence of hexamethylenetetramine. in Zeolites
Butterworth-Heinemann., 10(8), 802-805.
https://doi.org/https://doi.org/10.1016/0144-2449(90)90066-Z

Rajić N, Stojaković D, Kaučič V. Formation of AlPO4-15 and CoAPO-15 in the presence of hexamethylenetetramine. in Zeolites. 1990;10(8):802-805.
doi:https://doi.org/10.1016/0144-2449(90)90066-Z .

Rajić, Nevenka, Stojaković, Djordje, Kaučič, Venčeslav, "Formation of AlPO4-15 and CoAPO-15 in the presence of hexamethylenetetramine" in Zeolites, 10, no. 8 (1990):802-805,
https://doi.org/https://doi.org/10.1016/0144-2449(90)90066-Z . .

TY  - JOUR
AU  - Rajić, Nevenka
AU  - Kaučič, Venčeslav
AU  - Stojaković, Djordje
PY  - 1990
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5061
AB  - The hydrothermal synthesis of CoSAPO-14 and CoSAPO-34 in the presence of isopropylamine as the template is described. CoSAPO-14 is a new MeSAPO material that predominantly forms at 125°C, whereas CoSAPO-34 is the main product at 160°C. CoSAPO-14 has a triclinic and CoSAPO-34 has a trigonal unit cell. Both materials contain in their cavities a template that is hydrogen-bonded to the lattice. The synthesis in the presence of Co 2+ ions is much more sensitive to the composition of the reaction gel than is usually found in the preparation of SAPO materials.
PB  - Butterworth Publishers
T2  - Zeolites
T1  - Synthesis and characterization of the  CoSAPO- 14 and CoSAPO-34
EP  - 169
EP  - 173
IS  - 8
VL  - 10
DO  - 10.1016/0144-2449(90)90041-O
ER  - 

@article{
author = "Rajić, Nevenka and Kaučič, Venčeslav and Stojaković, Djordje",
year = "1990",
abstract = "The hydrothermal synthesis of CoSAPO-14 and CoSAPO-34 in the presence of isopropylamine as the template is described. CoSAPO-14 is a new MeSAPO material that predominantly forms at 125°C, whereas CoSAPO-34 is the main product at 160°C. CoSAPO-14 has a triclinic and CoSAPO-34 has a trigonal unit cell. Both materials contain in their cavities a template that is hydrogen-bonded to the lattice. The synthesis in the presence of Co 2+ ions is much more sensitive to the composition of the reaction gel than is usually found in the preparation of SAPO materials.",
publisher = "Butterworth Publishers",
journal = "Zeolites",
title = "Synthesis and characterization of the  CoSAPO- 14 and CoSAPO-34",
pages = "169-173",
number = "8",
volume = "10",
doi = "10.1016/0144-2449(90)90041-O"
}

Rajić, N., Kaučič, V.,& Stojaković, D.. (1990). Synthesis and characterization of the  CoSAPO- 14 and CoSAPO-34. in Zeolites
Butterworth Publishers., 10(8).
https://doi.org/10.1016/0144-2449(90)90041-O

Rajić N, Kaučič V, Stojaković D. Synthesis and characterization of the  CoSAPO- 14 and CoSAPO-34. in Zeolites. 1990;10(8):null-169.
doi:10.1016/0144-2449(90)90041-O .

Rajić, Nevenka, Kaučič, Venčeslav, Stojaković, Djordje, "Synthesis and characterization of the  CoSAPO- 14 and CoSAPO-34" in Zeolites, 10, no. 8 (1990),
https://doi.org/10.1016/0144-2449(90)90041-O . .

TY  - JOUR
AU  - Stojaković, Djordje
AU  - Rajić, Nevenka
PY  - 1990
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5057
AB  - In solutions of phthalocyanine, H2Pc, (c = 1–3 × 10−5 mol dm−3) and copper(II) chloride (c ≈ 10−3 mol dm−3) in sulfuric acid (c = 16–18 mol dm−3), two pseudo first-order reactions take place: (1) decomposition of H2Pc; (2) conversion of H2Pc into copper(II) phthalocyanine, CuPc. Reaction (1) is H2O concentration dependent and its rate constant increases from 0.088 to 1.88 h−1 as the H2SO4 concentration changes from 18 to 16 mol dm−3. The rate constant of (2) does not vary significantly with H2SO4 concentration and lies around the 0.05 h−1 mark. The CuPc formed in reaction (2) does not decompose under the above conditions.
PB  - Elsevier
T2  - Inorganica Chimica Acta
T1  - A Kinetic Study of the System Phthalocyanine-Copper(II) Chloride-Sulfuric Acid
EP  - 20
SP  - 17
VL  - 171
DO  - 10.1016/S0020-1693(00)84656-3
ER  - 

@article{
author = "Stojaković, Djordje and Rajić, Nevenka",
year = "1990",
abstract = "In solutions of phthalocyanine, H2Pc, (c = 1–3 × 10−5 mol dm−3) and copper(II) chloride (c ≈ 10−3 mol dm−3) in sulfuric acid (c = 16–18 mol dm−3), two pseudo first-order reactions take place: (1) decomposition of H2Pc; (2) conversion of H2Pc into copper(II) phthalocyanine, CuPc. Reaction (1) is H2O concentration dependent and its rate constant increases from 0.088 to 1.88 h−1 as the H2SO4 concentration changes from 18 to 16 mol dm−3. The rate constant of (2) does not vary significantly with H2SO4 concentration and lies around the 0.05 h−1 mark. The CuPc formed in reaction (2) does not decompose under the above conditions.",
publisher = "Elsevier",
journal = "Inorganica Chimica Acta",
title = "A Kinetic Study of the System Phthalocyanine-Copper(II) Chloride-Sulfuric Acid",
pages = "20-17",
volume = "171",
doi = "10.1016/S0020-1693(00)84656-3"
}

Stojaković, D.,& Rajić, N.. (1990). A Kinetic Study of the System Phthalocyanine-Copper(II) Chloride-Sulfuric Acid. in Inorganica Chimica Acta
Elsevier., 171, 17-20.
https://doi.org/10.1016/S0020-1693(00)84656-3

Stojaković D, Rajić N. A Kinetic Study of the System Phthalocyanine-Copper(II) Chloride-Sulfuric Acid. in Inorganica Chimica Acta. 1990;171:17-20.
doi:10.1016/S0020-1693(00)84656-3 .

Stojaković, Djordje, Rajić, Nevenka, "A Kinetic Study of the System Phthalocyanine-Copper(II) Chloride-Sulfuric Acid" in Inorganica Chimica Acta, 171 (1990):17-20,
https://doi.org/10.1016/S0020-1693(00)84656-3 . .

TY  - JOUR
AU  - Rajić, Nevenka
AU  - Stojaković, Djordje
PY  - 1989
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5099
AB  - Synthesis of the peripherally substituted (phthalocyaninato)metal derivatives (NO2)4PcM (M α Ni, Co, Cu; NO2 groups are in 1,8,15,22- or 2,9,16,23-positions) is described, and their X-ray powder diffraction patterns, solubilities, electronic and infrared spectra, and thermal stability are reported. The complexes exhibit isomorphism and polymorphism, and they are more soluble than the corresponding MPcs. Their thermal stability increases in the series Co < Ni < Cu, being at the same time greater for the 2,9,16,23-tetranitro- than for the 1,8,15,22-tetranitro derivatives.
PB  - Taylor & Francis
T2  - Journal of Coordination Chemistry
T1  - Synthesis and Characterization of Some Nitro-Substituted Phthalocyanines of Nickel(II), Cobalt(II) and Copper(II)
EP  - 301
SP  - 295
VL  - 19
DO  - 10.1080/00958978909408832
ER  - 

@article{
author = "Rajić, Nevenka and Stojaković, Djordje",
year = "1989",
abstract = "Synthesis of the peripherally substituted (phthalocyaninato)metal derivatives (NO2)4PcM (M α Ni, Co, Cu; NO2 groups are in 1,8,15,22- or 2,9,16,23-positions) is described, and their X-ray powder diffraction patterns, solubilities, electronic and infrared spectra, and thermal stability are reported. The complexes exhibit isomorphism and polymorphism, and they are more soluble than the corresponding MPcs. Their thermal stability increases in the series Co < Ni < Cu, being at the same time greater for the 2,9,16,23-tetranitro- than for the 1,8,15,22-tetranitro derivatives.",
publisher = "Taylor & Francis",
journal = "Journal of Coordination Chemistry",
title = "Synthesis and Characterization of Some Nitro-Substituted Phthalocyanines of Nickel(II), Cobalt(II) and Copper(II)",
pages = "301-295",
volume = "19",
doi = "10.1080/00958978909408832"
}

Rajić, N.,& Stojaković, D.. (1989). Synthesis and Characterization of Some Nitro-Substituted Phthalocyanines of Nickel(II), Cobalt(II) and Copper(II). in Journal of Coordination Chemistry
Taylor & Francis., 19, 295-301.
https://doi.org/10.1080/00958978909408832

Rajić N, Stojaković D. Synthesis and Characterization of Some Nitro-Substituted Phthalocyanines of Nickel(II), Cobalt(II) and Copper(II). in Journal of Coordination Chemistry. 1989;19:295-301.
doi:10.1080/00958978909408832 .

Rajić, Nevenka, Stojaković, Djordje, "Synthesis and Characterization of Some Nitro-Substituted Phthalocyanines of Nickel(II), Cobalt(II) and Copper(II)" in Journal of Coordination Chemistry, 19 (1989):295-301,
https://doi.org/10.1080/00958978909408832 . .

TY  - JOUR
AU  - Rajić, Nevenka
AU  - Stojaković, Djordje
PY  - 1989
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6393
AB  - The synthesis of (2-nitrophthalocyanato)copper(II) is described, and its X-ray powder diffraction pattern, solubility, electronic and infrared spectra, and thermal stability are reported. The product contains as an impurity about a 5% mass of unsubstituted phthalocyaninatocopper(II).
PB  - Serbian Chemical Society
T2  - Journal of Serbian Chemistry
T1  - Preparation and properties of (2-nitrophtalocyanato)copper(II)
EP  - 144
IS  - 4
SP  - 141
VL  - 54
UR  - https://hdl.handle.net/21.15107/rcub_technorep_6393
ER  - 

@article{
author = "Rajić, Nevenka and Stojaković, Djordje",
year = "1989",
abstract = "The synthesis of (2-nitrophthalocyanato)copper(II) is described, and its X-ray powder diffraction pattern, solubility, electronic and infrared spectra, and thermal stability are reported. The product contains as an impurity about a 5% mass of unsubstituted phthalocyaninatocopper(II).",
publisher = "Serbian Chemical Society",
journal = "Journal of Serbian Chemistry",
title = "Preparation and properties of (2-nitrophtalocyanato)copper(II)",
pages = "144-141",
number = "4",
volume = "54",
url = "https://hdl.handle.net/21.15107/rcub_technorep_6393"
}

Rajić, N.,& Stojaković, D.. (1989). Preparation and properties of (2-nitrophtalocyanato)copper(II). in Journal of Serbian Chemistry
Serbian Chemical Society., 54(4), 141-144.
https://hdl.handle.net/21.15107/rcub_technorep_6393

Rajić N, Stojaković D. Preparation and properties of (2-nitrophtalocyanato)copper(II). in Journal of Serbian Chemistry. 1989;54(4):141-144.
https://hdl.handle.net/21.15107/rcub_technorep_6393 .

Rajić, Nevenka, Stojaković, Djordje, "Preparation and properties of (2-nitrophtalocyanato)copper(II)" in Journal of Serbian Chemistry, 54, no. 4 (1989):141-144,
https://hdl.handle.net/21.15107/rcub_technorep_6393 .

TY  - JOUR
AU  - Rajić, Nevenka
AU  - Stojaković, Djordje
PY  - 1989
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6392
AB  - Synthesis of the peripherally substituted (phthalocyaninato)metal derivatives (NO2)4PcM (M α Ni, Co, Cu; NO2 groups are in 1,8,15,22- or 2,9,16,23-positions) is described, and their X-ray powder diffraction patterns, solubilities, electronic and infrared spectra, and thermal stability are reported. The complexes exhibit isomorphism and polymorphism, and they are more soluble than the corresponding MPcs. Their thermal stability increases in the series Co < Ni < Cu, being at the same time greater for the 2,9,16,23-tetranitro- than for the 1,8,15,22-tetranitro derivatives
PB  - Taylor&Francis
T2  - Journal of Coordination Chemistry
T1  - Synthesis and Characterization of Some Nitro-Substituted Phthalocyanines of Nickel(II), Cobalt(II) and Copper(II)
EP  - 301
IS  - 4
SP  - 295
VL  - 19
DO  - 10.1080/00958978909408832
ER  - 

@article{
author = "Rajić, Nevenka and Stojaković, Djordje",
year = "1989",
abstract = "Synthesis of the peripherally substituted (phthalocyaninato)metal derivatives (NO2)4PcM (M α Ni, Co, Cu; NO2 groups are in 1,8,15,22- or 2,9,16,23-positions) is described, and their X-ray powder diffraction patterns, solubilities, electronic and infrared spectra, and thermal stability are reported. The complexes exhibit isomorphism and polymorphism, and they are more soluble than the corresponding MPcs. Their thermal stability increases in the series Co < Ni < Cu, being at the same time greater for the 2,9,16,23-tetranitro- than for the 1,8,15,22-tetranitro derivatives",
publisher = "Taylor&Francis",
journal = "Journal of Coordination Chemistry",
title = "Synthesis and Characterization of Some Nitro-Substituted Phthalocyanines of Nickel(II), Cobalt(II) and Copper(II)",
pages = "301-295",
number = "4",
volume = "19",
doi = "10.1080/00958978909408832"
}

Rajić, N.,& Stojaković, D.. (1989). Synthesis and Characterization of Some Nitro-Substituted Phthalocyanines of Nickel(II), Cobalt(II) and Copper(II). in Journal of Coordination Chemistry
Taylor&Francis., 19(4), 295-301.
https://doi.org/10.1080/00958978909408832

Rajić N, Stojaković D. Synthesis and Characterization of Some Nitro-Substituted Phthalocyanines of Nickel(II), Cobalt(II) and Copper(II). in Journal of Coordination Chemistry. 1989;19(4):295-301.
doi:10.1080/00958978909408832 .

Rajić, Nevenka, Stojaković, Djordje, "Synthesis and Characterization of Some Nitro-Substituted Phthalocyanines of Nickel(II), Cobalt(II) and Copper(II)" in Journal of Coordination Chemistry, 19, no. 4 (1989):295-301,
https://doi.org/10.1080/00958978909408832 . .

TY  - JOUR
AU  - Nevenka, Rajić
AU  - Stojaković, Djordje
PY  - 1989
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6391
AB  - Treatment of an amorphous nickel(II)-substituted aluminosilicate (NiAS) with 1,2-diaminoethane (en),
1,2-diaminopropane (pnd) and 1,3-diaminopropane (tmd) gives materials (NiAS-en, NiAS-pnd and NiAS-tmd) that are characterized by Ni/diamine ratio of 1:2, 1:1 and 1:1, respectively. The Ni2+ coordination environment is octahedral for NiAS-tmd (as it is for NiAS), tetragonally distored octahedral for NiAS-en, and probably trigonal bypiramidal for NiAS-pnd. The tmd ligand in NiAS-tmd is coordinated as a monodentate.
PB  - Taylor & Francis
T2  - Journal of Coordination Chemistry
T1  - Diamine Incorporation in An Amorphous Nickel(II) Aluminosilicate
EP  - 167
SP  - 163
VL  - 20
UR  - https://hdl.handle.net/21.15107/rcub_technorep_6391
ER  - 

@article{
author = "Nevenka, Rajić and Stojaković, Djordje",
year = "1989",
abstract = "Treatment of an amorphous nickel(II)-substituted aluminosilicate (NiAS) with 1,2-diaminoethane (en),
1,2-diaminopropane (pnd) and 1,3-diaminopropane (tmd) gives materials (NiAS-en, NiAS-pnd and NiAS-tmd) that are characterized by Ni/diamine ratio of 1:2, 1:1 and 1:1, respectively. The Ni2+ coordination environment is octahedral for NiAS-tmd (as it is for NiAS), tetragonally distored octahedral for NiAS-en, and probably trigonal bypiramidal for NiAS-pnd. The tmd ligand in NiAS-tmd is coordinated as a monodentate.",
publisher = "Taylor & Francis",
journal = "Journal of Coordination Chemistry",
title = "Diamine Incorporation in An Amorphous Nickel(II) Aluminosilicate",
pages = "167-163",
volume = "20",
url = "https://hdl.handle.net/21.15107/rcub_technorep_6391"
}

Nevenka, R.,& Stojaković, D.. (1989). Diamine Incorporation in An Amorphous Nickel(II) Aluminosilicate. in Journal of Coordination Chemistry
Taylor & Francis., 20, 163-167.
https://hdl.handle.net/21.15107/rcub_technorep_6391

Nevenka R, Stojaković D. Diamine Incorporation in An Amorphous Nickel(II) Aluminosilicate. in Journal of Coordination Chemistry. 1989;20:163-167.
https://hdl.handle.net/21.15107/rcub_technorep_6391 .

Nevenka, Rajić, Stojaković, Djordje, "Diamine Incorporation in An Amorphous Nickel(II) Aluminosilicate" in Journal of Coordination Chemistry, 20 (1989):163-167,
https://hdl.handle.net/21.15107/rcub_technorep_6391 .

TY  - JOUR
AU  - Rajić, Nevenka
AU  - Stojaković, Đorđe
PY  - 1987
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5058
AB  - Amorphous aluminosilicates containing about 12 wt.%  nickel have been synthesized by cation exchange. Approximately 40 % of the nickel content is present in the form of octahedral [Ni(H20)6]2+ ions while the bulk of Ni2+ is coordinated both by H2O molecules and by oxygen atoms of the aluminosilicate framework. When the materials are heated in air at 350 oC, a change in the nickel coordination environment/geometry and possibly also a partial oxidation take place.
AB  - Amorfni aluminosilikati sa oko 12 mas. % nikla dobijeni su jonskom izmenom. Oko 40% nikla nalazi se u obliku oktaedarski koordiniranih jona [Ni(H20)6]2+, a preostali nikal koordiniran je sa molekulima vode i kiseonikovim atomima iz aluminosilikatne rešetke. Zagrevanjem na vazduhu, na oko 350 0C dolazi do promena u koordinaciji, odnosno geometriji nikla, a moguće je da dolazi i do delimične oksidacije nikla.
PB  - Hrvatsko kemijsko društvo
T2  - CROATICA CHEMICA  ACTA
T1  - Synthesis and Characterization of Amorphous Nickel(II) Aluminosilicate
EP  - 739
IS  - 4
SP  - 735
VL  - 60
UR  - https://hdl.handle.net/21.15107/rcub_technorep_5058
ER  - 

@article{
author = "Rajić, Nevenka and Stojaković, Đorđe",
year = "1987",
abstract = "Amorphous aluminosilicates containing about 12 wt.%  nickel have been synthesized by cation exchange. Approximately 40 % of the nickel content is present in the form of octahedral [Ni(H20)6]2+ ions while the bulk of Ni2+ is coordinated both by H2O molecules and by oxygen atoms of the aluminosilicate framework. When the materials are heated in air at 350 oC, a change in the nickel coordination environment/geometry and possibly also a partial oxidation take place., Amorfni aluminosilikati sa oko 12 mas. % nikla dobijeni su jonskom izmenom. Oko 40% nikla nalazi se u obliku oktaedarski koordiniranih jona [Ni(H20)6]2+, a preostali nikal koordiniran je sa molekulima vode i kiseonikovim atomima iz aluminosilikatne rešetke. Zagrevanjem na vazduhu, na oko 350 0C dolazi do promena u koordinaciji, odnosno geometriji nikla, a moguće je da dolazi i do delimične oksidacije nikla.",
publisher = "Hrvatsko kemijsko društvo",
journal = "CROATICA CHEMICA  ACTA",
title = "Synthesis and Characterization of Amorphous Nickel(II) Aluminosilicate",
pages = "739-735",
number = "4",
volume = "60",
url = "https://hdl.handle.net/21.15107/rcub_technorep_5058"
}

Rajić, N.,& Stojaković, Đ.. (1987). Synthesis and Characterization of Amorphous Nickel(II) Aluminosilicate. in CROATICA CHEMICA  ACTA
Hrvatsko kemijsko društvo., 60(4), 735-739.
https://hdl.handle.net/21.15107/rcub_technorep_5058

Rajić N, Stojaković Đ. Synthesis and Characterization of Amorphous Nickel(II) Aluminosilicate. in CROATICA CHEMICA  ACTA. 1987;60(4):735-739.
https://hdl.handle.net/21.15107/rcub_technorep_5058 .

Rajić, Nevenka, Stojaković, Đorđe, "Synthesis and Characterization of Amorphous Nickel(II) Aluminosilicate" in CROATICA CHEMICA  ACTA, 60, no. 4 (1987):735-739,
https://hdl.handle.net/21.15107/rcub_technorep_5058 .