TY  - JOUR
AU  - Šalipur, Hristina
AU  - Lončarević, Davor
AU  - Dostanić, Jasmina
AU  - Likozar, Blaž
AU  - Prašnikar, Anže
AU  - Manojlović, Dragan D.
PY  - 2022
UR  - https://www.sciencedirect.com/science/article/pii/S0360319922006036
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/5207
AB  - In this work hydrogen production activity of a series of the nickel-loaded, nitrogen-doped titanate-based photocatalysts was tested by water splitting reaction in isopropanol-water mixture. The utilization of ammonium ions during catalyst synthesis and subsequent calcination led to successful formation of nitrogen-doped nanotubular titanates with lower sodium content, favored titanate-to-anatase transformation and enhanced textural, morphological and interface properties. The photocatalytic tests revealed that hydrogen production activity of nitrogen-doped titanates is ten times higher compared to nitrogen-free titanates. The presence of highly photoactive anatase phase, improved anatase crystallinity and lower amount of sodium ions are found to be decisive factors for increased hydrogen production activity. The optimal nickel loading was determined and the variation in photocatalytic activity with reduction temperature was explained. Stability tests gave quantitative analysis of the effects of reaction products accumulation and photocorrosion on the catalyst deactivation.
PB  - Elsevier
T2  - International Journal of Hydrogen Energy
T1  - Nickel-loaded nitrogen-doped titanate nanostructured catalysts for solar-light driven hydrogen evolution and environmental remediation
VL  - 47
IS  - 26
SP  - 12937
EP  - 12952
DO  - 10.1016/j.ijhydene.2022.02.054
ER  - 

@article{
author = "Šalipur, Hristina and Lončarević, Davor and Dostanić, Jasmina and Likozar, Blaž and Prašnikar, Anže and Manojlović, Dragan D.",
year = "2022",
abstract = "In this work hydrogen production activity of a series of the nickel-loaded, nitrogen-doped titanate-based photocatalysts was tested by water splitting reaction in isopropanol-water mixture. The utilization of ammonium ions during catalyst synthesis and subsequent calcination led to successful formation of nitrogen-doped nanotubular titanates with lower sodium content, favored titanate-to-anatase transformation and enhanced textural, morphological and interface properties. The photocatalytic tests revealed that hydrogen production activity of nitrogen-doped titanates is ten times higher compared to nitrogen-free titanates. The presence of highly photoactive anatase phase, improved anatase crystallinity and lower amount of sodium ions are found to be decisive factors for increased hydrogen production activity. The optimal nickel loading was determined and the variation in photocatalytic activity with reduction temperature was explained. Stability tests gave quantitative analysis of the effects of reaction products accumulation and photocorrosion on the catalyst deactivation.",
publisher = "Elsevier",
journal = "International Journal of Hydrogen Energy",
title = "Nickel-loaded nitrogen-doped titanate nanostructured catalysts for solar-light driven hydrogen evolution and environmental remediation",
volume = "47",
number = "26",
pages = "12937-12952",
doi = "10.1016/j.ijhydene.2022.02.054"
}

Šalipur, H., Lončarević, D., Dostanić, J., Likozar, B., Prašnikar, A.,& Manojlović, D. D.. (2022). Nickel-loaded nitrogen-doped titanate nanostructured catalysts for solar-light driven hydrogen evolution and environmental remediation. in International Journal of Hydrogen Energy
Elsevier., 47(26), 12937-12952.
https://doi.org/10.1016/j.ijhydene.2022.02.054

Šalipur H, Lončarević D, Dostanić J, Likozar B, Prašnikar A, Manojlović DD. Nickel-loaded nitrogen-doped titanate nanostructured catalysts for solar-light driven hydrogen evolution and environmental remediation. in International Journal of Hydrogen Energy. 2022;47(26):12937-12952.
doi:10.1016/j.ijhydene.2022.02.054 .

Šalipur, Hristina, Lončarević, Davor, Dostanić, Jasmina, Likozar, Blaž, Prašnikar, Anže, Manojlović, Dragan D., "Nickel-loaded nitrogen-doped titanate nanostructured catalysts for solar-light driven hydrogen evolution and environmental remediation" in International Journal of Hydrogen Energy, 47, no. 26 (2022):12937-12952,
https://doi.org/10.1016/j.ijhydene.2022.02.054 . .

TY  - JOUR
AU  - Šoštarić, Tatjana D.
AU  - Petrović, Marija S.
AU  - Pastor, Ferenc
AU  - Lončarević, Davor
AU  - Petrović, Jelena T.
AU  - Milojković, Jelena V.
AU  - Stojanović, Mirjana D.
PY  - 2018
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2152
AB  - Locally available apricot (Prunus armeniaca L.) shells classified as a waste product from fruit processing, were alkali activated in order to develop an efficient heavy metal ions sorbent for water purification. To examine the changes occurred after alkali treatment, raw (SH) and modified apricot shells (SHM) were thoroughly characterized in terms of their chemical composition and surface properties. Chemical analysis revealed that alkaline treatment causes the disintegration of hemicellulose (its content decreased from 19.2 to 3.5%), which was in accordance with FTIR results. SEM micrographs and the mercury intrusion porosimetry revealed a larger surface area and porosity of SHM. Bohem's acid-base titration method indicated that the most of the SHM surface carboxylic groups were in sodium salt form and together with the pH of points of zero charge showed increase of surface alkalinity after modification. Treatment with NaOH enhanced the adsorption capacity by 154, 61 and 90% for Cu2+, Zn2+ and Pb2+, respectively. The amount of cations released from SHM was almost equal to the amount of adsorbed metal ions, suggesting ion exchange mechanism. The pseudo-second order kinetic indicated that the heavy metals cations were bound predominantly by complexation. In order to establish the effectiveness of the biosorbent in real wastewater sample, SHM was employed for cleaning-up of drain water emanating from atomic adsorption spectrophotometer. The SHM showed high removal efficiency towards multiple metal ions. The amounts of Fe, Pb, Cu and Cr ions were reduced by 97, 87, 81 and 80%, respectively, while Ni and Zn amounts were reduced for 33 and 14%. Used biosorbent SHM can be successfully regenerated with HCl (desorption  gt  95%) and after regeneration biosorbent can be reused or it can be safely disposed. (C) 2018 Elsevier B.V. All rights reserved.
PB  - Elsevier Science Bv, Amsterdam
T2  - Journal of Molecular Liquids
T1  - Study of heavy metals biosorption on native and alkali-treated apricot shells and its application in wastewater treatment
VL  - 259
SP  - 340
EP  - 349
DO  - 10.1016/j.molliq.2018.03.055
ER  - 

@article{
author = "Šoštarić, Tatjana D. and Petrović, Marija S. and Pastor, Ferenc and Lončarević, Davor and Petrović, Jelena T. and Milojković, Jelena V. and Stojanović, Mirjana D.",
year = "2018",
abstract = "Locally available apricot (Prunus armeniaca L.) shells classified as a waste product from fruit processing, were alkali activated in order to develop an efficient heavy metal ions sorbent for water purification. To examine the changes occurred after alkali treatment, raw (SH) and modified apricot shells (SHM) were thoroughly characterized in terms of their chemical composition and surface properties. Chemical analysis revealed that alkaline treatment causes the disintegration of hemicellulose (its content decreased from 19.2 to 3.5%), which was in accordance with FTIR results. SEM micrographs and the mercury intrusion porosimetry revealed a larger surface area and porosity of SHM. Bohem's acid-base titration method indicated that the most of the SHM surface carboxylic groups were in sodium salt form and together with the pH of points of zero charge showed increase of surface alkalinity after modification. Treatment with NaOH enhanced the adsorption capacity by 154, 61 and 90% for Cu2+, Zn2+ and Pb2+, respectively. The amount of cations released from SHM was almost equal to the amount of adsorbed metal ions, suggesting ion exchange mechanism. The pseudo-second order kinetic indicated that the heavy metals cations were bound predominantly by complexation. In order to establish the effectiveness of the biosorbent in real wastewater sample, SHM was employed for cleaning-up of drain water emanating from atomic adsorption spectrophotometer. The SHM showed high removal efficiency towards multiple metal ions. The amounts of Fe, Pb, Cu and Cr ions were reduced by 97, 87, 81 and 80%, respectively, while Ni and Zn amounts were reduced for 33 and 14%. Used biosorbent SHM can be successfully regenerated with HCl (desorption  gt  95%) and after regeneration biosorbent can be reused or it can be safely disposed. (C) 2018 Elsevier B.V. All rights reserved.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Journal of Molecular Liquids",
title = "Study of heavy metals biosorption on native and alkali-treated apricot shells and its application in wastewater treatment",
volume = "259",
pages = "340-349",
doi = "10.1016/j.molliq.2018.03.055"
}

Šoštarić, T. D., Petrović, M. S., Pastor, F., Lončarević, D., Petrović, J. T., Milojković, J. V.,& Stojanović, M. D.. (2018). Study of heavy metals biosorption on native and alkali-treated apricot shells and its application in wastewater treatment. in Journal of Molecular Liquids
Elsevier Science Bv, Amsterdam., 259, 340-349.
https://doi.org/10.1016/j.molliq.2018.03.055

Šoštarić TD, Petrović MS, Pastor F, Lončarević D, Petrović JT, Milojković JV, Stojanović MD. Study of heavy metals biosorption on native and alkali-treated apricot shells and its application in wastewater treatment. in Journal of Molecular Liquids. 2018;259:340-349.
doi:10.1016/j.molliq.2018.03.055 .

Šoštarić, Tatjana D., Petrović, Marija S., Pastor, Ferenc, Lončarević, Davor, Petrović, Jelena T., Milojković, Jelena V., Stojanović, Mirjana D., "Study of heavy metals biosorption on native and alkali-treated apricot shells and its application in wastewater treatment" in Journal of Molecular Liquids, 259 (2018):340-349,
https://doi.org/10.1016/j.molliq.2018.03.055 . .

TY  - DATA
AU  - Šoštarić, Tatjana D.
AU  - Petrović, Marija S.
AU  - Pastor, Ferenc
AU  - Lončarević, Davor
AU  - Petrović, Jelena T.
AU  - Milojković, Jelena V.
AU  - Stojanović, Mirjana D.
PY  - 2018
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2969
PB  - Elsevier Science Bv, Amsterdam
T2  - Journal of Molecular Liquids
T1  - Supplementary material for the article: Šoštarić, T. D.; Petrović, M. S.; Pastor, F. T.; Lončarević, D. R.; Petrović, J. T.; Milojković,  J. V.; Stojanović, M. D. Study of Heavy Metals Biosorption on Native and Alkali-Treated  Apricot Shells and Its Application in Wastewater Treatment. Journal of Molecular Liquids  2018, 259, 340–349. https://doi.org/10.1016/j.molliq.2018.03.055
UR  - https://hdl.handle.net/21.15107/rcub_cherry_2969
ER  - 

@misc{
author = "Šoštarić, Tatjana D. and Petrović, Marija S. and Pastor, Ferenc and Lončarević, Davor and Petrović, Jelena T. and Milojković, Jelena V. and Stojanović, Mirjana D.",
year = "2018",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Journal of Molecular Liquids",
title = "Supplementary material for the article: Šoštarić, T. D.; Petrović, M. S.; Pastor, F. T.; Lončarević, D. R.; Petrović, J. T.; Milojković,  J. V.; Stojanović, M. D. Study of Heavy Metals Biosorption on Native and Alkali-Treated  Apricot Shells and Its Application in Wastewater Treatment. Journal of Molecular Liquids  2018, 259, 340–349. https://doi.org/10.1016/j.molliq.2018.03.055",
url = "https://hdl.handle.net/21.15107/rcub_cherry_2969"
}

Šoštarić, T. D., Petrović, M. S., Pastor, F., Lončarević, D., Petrović, J. T., Milojković, J. V.,& Stojanović, M. D.. (2018). Supplementary material for the article: Šoštarić, T. D.; Petrović, M. S.; Pastor, F. T.; Lončarević, D. R.; Petrović, J. T.; Milojković,  J. V.; Stojanović, M. D. Study of Heavy Metals Biosorption on Native and Alkali-Treated  Apricot Shells and Its Application in Wastewater Treatment. Journal of Molecular Liquids  2018, 259, 340–349. https://doi.org/10.1016/j.molliq.2018.03.055. in Journal of Molecular Liquids
Elsevier Science Bv, Amsterdam..
https://hdl.handle.net/21.15107/rcub_cherry_2969

Šoštarić TD, Petrović MS, Pastor F, Lončarević D, Petrović JT, Milojković JV, Stojanović MD. Supplementary material for the article: Šoštarić, T. D.; Petrović, M. S.; Pastor, F. T.; Lončarević, D. R.; Petrović, J. T.; Milojković,  J. V.; Stojanović, M. D. Study of Heavy Metals Biosorption on Native and Alkali-Treated  Apricot Shells and Its Application in Wastewater Treatment. Journal of Molecular Liquids  2018, 259, 340–349. https://doi.org/10.1016/j.molliq.2018.03.055. in Journal of Molecular Liquids. 2018;.
https://hdl.handle.net/21.15107/rcub_cherry_2969 .

Šoštarić, Tatjana D., Petrović, Marija S., Pastor, Ferenc, Lončarević, Davor, Petrović, Jelena T., Milojković, Jelena V., Stojanović, Mirjana D., "Supplementary material for the article: Šoštarić, T. D.; Petrović, M. S.; Pastor, F. T.; Lončarević, D. R.; Petrović, J. T.; Milojković,  J. V.; Stojanović, M. D. Study of Heavy Metals Biosorption on Native and Alkali-Treated  Apricot Shells and Its Application in Wastewater Treatment. Journal of Molecular Liquids  2018, 259, 340–349. https://doi.org/10.1016/j.molliq.2018.03.055" in Journal of Molecular Liquids (2018),
https://hdl.handle.net/21.15107/rcub_cherry_2969 .

TY  - JOUR
AU  - Šoštarić, Tatjana D.
AU  - Petrović, Marija S.
AU  - Pastor, Ferenc
AU  - Lončarević, Davor
AU  - Petrović, Jelena T.
AU  - Milojković, Jelena V.
AU  - Stojanović, Mirjana D.
PY  - 2018
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2970
AB  - Locally available apricot (Prunus armeniaca L.) shells classified as a waste product from fruit processing, were alkali activated in order to develop an efficient heavy metal ions sorbent for water purification. To examine the changes occurred after alkali treatment, raw (SH) and modified apricot shells (SHM) were thoroughly characterized in terms of their chemical composition and surface properties. Chemical analysis revealed that alkaline treatment causes the disintegration of hemicellulose (its content decreased from 19.2 to 3.5%), which was in accordance with FTIR results. SEM micrographs and the mercury intrusion porosimetry revealed a larger surface area and porosity of SHM. Bohem's acid-base titration method indicated that the most of the SHM surface carboxylic groups were in sodium salt form and together with the pH of points of zero charge showed increase of surface alkalinity after modification. Treatment with NaOH enhanced the adsorption capacity by 154, 61 and 90% for Cu2+, Zn2+ and Pb2+, respectively. The amount of cations released from SHM was almost equal to the amount of adsorbed metal ions, suggesting ion exchange mechanism. The pseudo-second order kinetic indicated that the heavy metals cations were bound predominantly by complexation. In order to establish the effectiveness of the biosorbent in real wastewater sample, SHM was employed for cleaning-up of drain water emanating from atomic adsorption spectrophotometer. The SHM showed high removal efficiency towards multiple metal ions. The amounts of Fe, Pb, Cu and Cr ions were reduced by 97, 87, 81 and 80%, respectively, while Ni and Zn amounts were reduced for 33 and 14%. Used biosorbent SHM can be successfully regenerated with HCl (desorption  gt  95%) and after regeneration biosorbent can be reused or it can be safely disposed. (C) 2018 Elsevier B.V. All rights reserved.
PB  - Elsevier Science Bv, Amsterdam
T2  - Journal of Molecular Liquids
T1  - Study of heavy metals biosorption on native and alkali-treated apricot shells and its application in wastewater treatment
VL  - 259
SP  - 340
EP  - 349
DO  - 10.1016/j.molliq.2018.03.055
ER  - 

@article{
author = "Šoštarić, Tatjana D. and Petrović, Marija S. and Pastor, Ferenc and Lončarević, Davor and Petrović, Jelena T. and Milojković, Jelena V. and Stojanović, Mirjana D.",
year = "2018",
abstract = "Locally available apricot (Prunus armeniaca L.) shells classified as a waste product from fruit processing, were alkali activated in order to develop an efficient heavy metal ions sorbent for water purification. To examine the changes occurred after alkali treatment, raw (SH) and modified apricot shells (SHM) were thoroughly characterized in terms of their chemical composition and surface properties. Chemical analysis revealed that alkaline treatment causes the disintegration of hemicellulose (its content decreased from 19.2 to 3.5%), which was in accordance with FTIR results. SEM micrographs and the mercury intrusion porosimetry revealed a larger surface area and porosity of SHM. Bohem's acid-base titration method indicated that the most of the SHM surface carboxylic groups were in sodium salt form and together with the pH of points of zero charge showed increase of surface alkalinity after modification. Treatment with NaOH enhanced the adsorption capacity by 154, 61 and 90% for Cu2+, Zn2+ and Pb2+, respectively. The amount of cations released from SHM was almost equal to the amount of adsorbed metal ions, suggesting ion exchange mechanism. The pseudo-second order kinetic indicated that the heavy metals cations were bound predominantly by complexation. In order to establish the effectiveness of the biosorbent in real wastewater sample, SHM was employed for cleaning-up of drain water emanating from atomic adsorption spectrophotometer. The SHM showed high removal efficiency towards multiple metal ions. The amounts of Fe, Pb, Cu and Cr ions were reduced by 97, 87, 81 and 80%, respectively, while Ni and Zn amounts were reduced for 33 and 14%. Used biosorbent SHM can be successfully regenerated with HCl (desorption  gt  95%) and after regeneration biosorbent can be reused or it can be safely disposed. (C) 2018 Elsevier B.V. All rights reserved.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Journal of Molecular Liquids",
title = "Study of heavy metals biosorption on native and alkali-treated apricot shells and its application in wastewater treatment",
volume = "259",
pages = "340-349",
doi = "10.1016/j.molliq.2018.03.055"
}

Šoštarić, T. D., Petrović, M. S., Pastor, F., Lončarević, D., Petrović, J. T., Milojković, J. V.,& Stojanović, M. D.. (2018). Study of heavy metals biosorption on native and alkali-treated apricot shells and its application in wastewater treatment. in Journal of Molecular Liquids
Elsevier Science Bv, Amsterdam., 259, 340-349.
https://doi.org/10.1016/j.molliq.2018.03.055

Šoštarić TD, Petrović MS, Pastor F, Lončarević D, Petrović JT, Milojković JV, Stojanović MD. Study of heavy metals biosorption on native and alkali-treated apricot shells and its application in wastewater treatment. in Journal of Molecular Liquids. 2018;259:340-349.
doi:10.1016/j.molliq.2018.03.055 .

Šoštarić, Tatjana D., Petrović, Marija S., Pastor, Ferenc, Lončarević, Davor, Petrović, Jelena T., Milojković, Jelena V., Stojanović, Mirjana D., "Study of heavy metals biosorption on native and alkali-treated apricot shells and its application in wastewater treatment" in Journal of Molecular Liquids, 259 (2018):340-349,
https://doi.org/10.1016/j.molliq.2018.03.055 . .

TY  - JOUR
AU  - Dostanić, Jasmina
AU  - Lončarević, Davor
AU  - Zlatar, Matija
AU  - Vlahović, Filip
AU  - Jovanović, Dušan M.
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3579
AB  - A series of arylazo pyridone dyes was synthesized by changing the type of the substituent group in the diazo moiety, ranging from strong electron-donating to strong electron-withdrawing groups. The structural and electronic properties of the investigated dyes was calculated at the M062X/6-31 + G(d,p) level of theory. The observed good linear correlations between atomic charges and Hammett sigma(p) constants provided a basis to discuss the transmission of electronic substituent effects through a dye framework. The reactivity of synthesized dyes was tested through their decolorization efficiency in TiO2 photocatalytic system (Degussa P-25). Quantitative structure activity relationship analysis revealed a strong correlation between reactivity of investigated dyes and Hammett substituent constants. The reaction was facilitated by electron-withdrawing groups, and retarded by electron-donating ones. Quantum mechanical calculations was used in order to describe the mechanism of the photocatalytic oxidation reactions of investigated dyes and interpret their reactivities within the framework of the Density Functional Theory (DFT). According to DFT based reactivity descriptors, i.e. Fukui functions and local softness, the active site moves from azo nitrogen atom linked to benzene ring to pyridone carbon atom linked to azo bond, going from dyes with electron-donating groups to dyes with electron-withdrawing groups.
PB  - Elsevier Science Bv, Amsterdam
T2  - Journal of Hazardous Materials
T1  - Quantitative structure-activity relationship analysis of substituted arylazo pyridone dyes in photocatalytic system: Experimental and theoretical study
VL  - 316
SP  - 26
EP  - 33
DO  - 10.1016/j.jhazmat.2016.05.015
ER  - 

@article{
author = "Dostanić, Jasmina and Lončarević, Davor and Zlatar, Matija and Vlahović, Filip and Jovanović, Dušan M.",
year = "2016",
abstract = "A series of arylazo pyridone dyes was synthesized by changing the type of the substituent group in the diazo moiety, ranging from strong electron-donating to strong electron-withdrawing groups. The structural and electronic properties of the investigated dyes was calculated at the M062X/6-31 + G(d,p) level of theory. The observed good linear correlations between atomic charges and Hammett sigma(p) constants provided a basis to discuss the transmission of electronic substituent effects through a dye framework. The reactivity of synthesized dyes was tested through their decolorization efficiency in TiO2 photocatalytic system (Degussa P-25). Quantitative structure activity relationship analysis revealed a strong correlation between reactivity of investigated dyes and Hammett substituent constants. The reaction was facilitated by electron-withdrawing groups, and retarded by electron-donating ones. Quantum mechanical calculations was used in order to describe the mechanism of the photocatalytic oxidation reactions of investigated dyes and interpret their reactivities within the framework of the Density Functional Theory (DFT). According to DFT based reactivity descriptors, i.e. Fukui functions and local softness, the active site moves from azo nitrogen atom linked to benzene ring to pyridone carbon atom linked to azo bond, going from dyes with electron-donating groups to dyes with electron-withdrawing groups.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Journal of Hazardous Materials",
title = "Quantitative structure-activity relationship analysis of substituted arylazo pyridone dyes in photocatalytic system: Experimental and theoretical study",
volume = "316",
pages = "26-33",
doi = "10.1016/j.jhazmat.2016.05.015"
}

Dostanić, J., Lončarević, D., Zlatar, M., Vlahović, F.,& Jovanović, D. M.. (2016). Quantitative structure-activity relationship analysis of substituted arylazo pyridone dyes in photocatalytic system: Experimental and theoretical study. in Journal of Hazardous Materials
Elsevier Science Bv, Amsterdam., 316, 26-33.
https://doi.org/10.1016/j.jhazmat.2016.05.015

Dostanić J, Lončarević D, Zlatar M, Vlahović F, Jovanović DM. Quantitative structure-activity relationship analysis of substituted arylazo pyridone dyes in photocatalytic system: Experimental and theoretical study. in Journal of Hazardous Materials. 2016;316:26-33.
doi:10.1016/j.jhazmat.2016.05.015 .

Dostanić, Jasmina, Lončarević, Davor, Zlatar, Matija, Vlahović, Filip, Jovanović, Dušan M., "Quantitative structure-activity relationship analysis of substituted arylazo pyridone dyes in photocatalytic system: Experimental and theoretical study" in Journal of Hazardous Materials, 316 (2016):26-33,
https://doi.org/10.1016/j.jhazmat.2016.05.015 . .

TY  - DATA
AU  - Dostanić, Jasmina
AU  - Lončarević, Davor
AU  - Zlatar, Matija
AU  - Vlahović, Filip
AU  - Jovanović, Dušan M.
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3584
PB  - Elsevier Science Bv, Amsterdam
T2  - Journal of Hazardous Materials
T1  - Supplementary material for the article: Dostanić, J.; Lončarević, D.; Zlatar, M.; Vlahović, F.; Jovanović, D. M. Quantitative Structure-Activity Relationship Analysis of Substituted Arylazo Pyridone Dyes in Photocatalytic System: Experimental and Theoretical Study. J. Hazard. Mater. 2016, 316, 26–33. https://doi.org/10.1016/j.jhazmat.2016.05.015
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3584
ER  - 

@misc{
author = "Dostanić, Jasmina and Lončarević, Davor and Zlatar, Matija and Vlahović, Filip and Jovanović, Dušan M.",
year = "2016",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Journal of Hazardous Materials",
title = "Supplementary material for the article: Dostanić, J.; Lončarević, D.; Zlatar, M.; Vlahović, F.; Jovanović, D. M. Quantitative Structure-Activity Relationship Analysis of Substituted Arylazo Pyridone Dyes in Photocatalytic System: Experimental and Theoretical Study. J. Hazard. Mater. 2016, 316, 26–33. https://doi.org/10.1016/j.jhazmat.2016.05.015",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3584"
}

Dostanić, J., Lončarević, D., Zlatar, M., Vlahović, F.,& Jovanović, D. M.. (2016). Supplementary material for the article: Dostanić, J.; Lončarević, D.; Zlatar, M.; Vlahović, F.; Jovanović, D. M. Quantitative Structure-Activity Relationship Analysis of Substituted Arylazo Pyridone Dyes in Photocatalytic System: Experimental and Theoretical Study. J. Hazard. Mater. 2016, 316, 26–33. https://doi.org/10.1016/j.jhazmat.2016.05.015. in Journal of Hazardous Materials
Elsevier Science Bv, Amsterdam..
https://hdl.handle.net/21.15107/rcub_cherry_3584

Dostanić J, Lončarević D, Zlatar M, Vlahović F, Jovanović DM. Supplementary material for the article: Dostanić, J.; Lončarević, D.; Zlatar, M.; Vlahović, F.; Jovanović, D. M. Quantitative Structure-Activity Relationship Analysis of Substituted Arylazo Pyridone Dyes in Photocatalytic System: Experimental and Theoretical Study. J. Hazard. Mater. 2016, 316, 26–33. https://doi.org/10.1016/j.jhazmat.2016.05.015. in Journal of Hazardous Materials. 2016;.
https://hdl.handle.net/21.15107/rcub_cherry_3584 .

Dostanić, Jasmina, Lončarević, Davor, Zlatar, Matija, Vlahović, Filip, Jovanović, Dušan M., "Supplementary material for the article: Dostanić, J.; Lončarević, D.; Zlatar, M.; Vlahović, F.; Jovanović, D. M. Quantitative Structure-Activity Relationship Analysis of Substituted Arylazo Pyridone Dyes in Photocatalytic System: Experimental and Theoretical Study. J. Hazard. Mater. 2016, 316, 26–33. https://doi.org/10.1016/j.jhazmat.2016.05.015" in Journal of Hazardous Materials (2016),
https://hdl.handle.net/21.15107/rcub_cherry_3584 .

TY  - JOUR
AU  - Dostanić, Jasmina
AU  - Lončarević, Davor
AU  - Zlatar, Matija
AU  - Vlahović, Filip
AU  - Jovanović, Dušan M.
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2277
AB  - A series of arylazo pyridone dyes was synthesized by changing the type of the substituent group in the diazo moiety, ranging from strong electron-donating to strong electron-withdrawing groups. The structural and electronic properties of the investigated dyes was calculated at the M062X/6-31 + G(d,p) level of theory. The observed good linear correlations between atomic charges and Hammett sigma(p) constants provided a basis to discuss the transmission of electronic substituent effects through a dye framework. The reactivity of synthesized dyes was tested through their decolorization efficiency in TiO2 photocatalytic system (Degussa P-25). Quantitative structure activity relationship analysis revealed a strong correlation between reactivity of investigated dyes and Hammett substituent constants. The reaction was facilitated by electron-withdrawing groups, and retarded by electron-donating ones. Quantum mechanical calculations was used in order to describe the mechanism of the photocatalytic oxidation reactions of investigated dyes and interpret their reactivities within the framework of the Density Functional Theory (DFT). According to DFT based reactivity descriptors, i.e. Fukui functions and local softness, the active site moves from azo nitrogen atom linked to benzene ring to pyridone carbon atom linked to azo bond, going from dyes with electron-donating groups to dyes with electron-withdrawing groups.
PB  - Elsevier Science Bv, Amsterdam
T2  - Journal of Hazardous Materials
T1  - Quantitative structure-activity relationship analysis of substituted arylazo pyridone dyes in photocatalytic system: Experimental and theoretical study
VL  - 316
SP  - 26
EP  - 33
DO  - 10.1016/j.jhazmat.2016.05.015
ER  - 

@article{
author = "Dostanić, Jasmina and Lončarević, Davor and Zlatar, Matija and Vlahović, Filip and Jovanović, Dušan M.",
year = "2016",
abstract = "A series of arylazo pyridone dyes was synthesized by changing the type of the substituent group in the diazo moiety, ranging from strong electron-donating to strong electron-withdrawing groups. The structural and electronic properties of the investigated dyes was calculated at the M062X/6-31 + G(d,p) level of theory. The observed good linear correlations between atomic charges and Hammett sigma(p) constants provided a basis to discuss the transmission of electronic substituent effects through a dye framework. The reactivity of synthesized dyes was tested through their decolorization efficiency in TiO2 photocatalytic system (Degussa P-25). Quantitative structure activity relationship analysis revealed a strong correlation between reactivity of investigated dyes and Hammett substituent constants. The reaction was facilitated by electron-withdrawing groups, and retarded by electron-donating ones. Quantum mechanical calculations was used in order to describe the mechanism of the photocatalytic oxidation reactions of investigated dyes and interpret their reactivities within the framework of the Density Functional Theory (DFT). According to DFT based reactivity descriptors, i.e. Fukui functions and local softness, the active site moves from azo nitrogen atom linked to benzene ring to pyridone carbon atom linked to azo bond, going from dyes with electron-donating groups to dyes with electron-withdrawing groups.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Journal of Hazardous Materials",
title = "Quantitative structure-activity relationship analysis of substituted arylazo pyridone dyes in photocatalytic system: Experimental and theoretical study",
volume = "316",
pages = "26-33",
doi = "10.1016/j.jhazmat.2016.05.015"
}

Dostanić, J., Lončarević, D., Zlatar, M., Vlahović, F.,& Jovanović, D. M.. (2016). Quantitative structure-activity relationship analysis of substituted arylazo pyridone dyes in photocatalytic system: Experimental and theoretical study. in Journal of Hazardous Materials
Elsevier Science Bv, Amsterdam., 316, 26-33.
https://doi.org/10.1016/j.jhazmat.2016.05.015

Dostanić J, Lončarević D, Zlatar M, Vlahović F, Jovanović DM. Quantitative structure-activity relationship analysis of substituted arylazo pyridone dyes in photocatalytic system: Experimental and theoretical study. in Journal of Hazardous Materials. 2016;316:26-33.
doi:10.1016/j.jhazmat.2016.05.015 .

Dostanić, Jasmina, Lončarević, Davor, Zlatar, Matija, Vlahović, Filip, Jovanović, Dušan M., "Quantitative structure-activity relationship analysis of substituted arylazo pyridone dyes in photocatalytic system: Experimental and theoretical study" in Journal of Hazardous Materials, 316 (2016):26-33,
https://doi.org/10.1016/j.jhazmat.2016.05.015 . .

TY  - JOUR
AU  - Lončarević, Davor
AU  - Krstic, J.
AU  - Dostanić, Jasmina
AU  - Manojlović, Dragan D.
AU  - Cupic, Z.
AU  - Jovanović, Dušan M.
PY  - 2010
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1047
AB  - Polymer supported catalysts with Co(II) and Cr(VI) ions were prepared and characterized by means of FTIR, diffuse reflectance UV-vis, nitrogen physisorption, mercury porosimetry and SEM-EDX measurements. The catalytic activity and selectivity of the polymer supported catalysts were tested in aerobic liquid-phase partial oxidation of cyclohexane in a polytetrafluoroethylene lined reactor. The influence of reaction time and temperature, main products addition, mass of the catalyst and different metals loading was investigated. Product yield and cyclohexyl hydroperoxide formation in the catalytic system were used as critical parameters which could be optimized by changing the cobalt content on the polymer and the catalyst mass used in the catalytic runs. By increasing cobalt content, a higher activity and corresponding lower selectivity towards cyclohexanone were obtained. This study indicates that the selectivity towards cyclohexanone and cyclohexanol is mainly defined by the yield and type of the catalyst with minor influence of temperature and main products addition. In addition catalysts were used for deperoxidation of cyclohexyl hydroperoxide in mild conditions. Nearly the same selectivity towards cyclohexanone and cyclohexanol is achieved using the cobalt containing catalyst, while a higher selectivity towards cyclohexanone is achieved using the chromium containing catalysts. (C) 2009 Elsevier B. V. All rights reserved.
PB  - Elsevier Science Sa, Lausanne
T2  - Chemical Engineering Journal
T1  - Cyclohexane oxidation and cyclohexyl hydroperoxide decomposition by poly(4-vinylpyridine-co-divinylbenzene) supported cobalt and chromium complexes
VL  - 157
IS  - 1
SP  - 181
EP  - 188
DO  - 10.1016/j.cej.2009.11.034
ER  - 

@article{
author = "Lončarević, Davor and Krstic, J. and Dostanić, Jasmina and Manojlović, Dragan D. and Cupic, Z. and Jovanović, Dušan M.",
year = "2010",
abstract = "Polymer supported catalysts with Co(II) and Cr(VI) ions were prepared and characterized by means of FTIR, diffuse reflectance UV-vis, nitrogen physisorption, mercury porosimetry and SEM-EDX measurements. The catalytic activity and selectivity of the polymer supported catalysts were tested in aerobic liquid-phase partial oxidation of cyclohexane in a polytetrafluoroethylene lined reactor. The influence of reaction time and temperature, main products addition, mass of the catalyst and different metals loading was investigated. Product yield and cyclohexyl hydroperoxide formation in the catalytic system were used as critical parameters which could be optimized by changing the cobalt content on the polymer and the catalyst mass used in the catalytic runs. By increasing cobalt content, a higher activity and corresponding lower selectivity towards cyclohexanone were obtained. This study indicates that the selectivity towards cyclohexanone and cyclohexanol is mainly defined by the yield and type of the catalyst with minor influence of temperature and main products addition. In addition catalysts were used for deperoxidation of cyclohexyl hydroperoxide in mild conditions. Nearly the same selectivity towards cyclohexanone and cyclohexanol is achieved using the cobalt containing catalyst, while a higher selectivity towards cyclohexanone is achieved using the chromium containing catalysts. (C) 2009 Elsevier B. V. All rights reserved.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Chemical Engineering Journal",
title = "Cyclohexane oxidation and cyclohexyl hydroperoxide decomposition by poly(4-vinylpyridine-co-divinylbenzene) supported cobalt and chromium complexes",
volume = "157",
number = "1",
pages = "181-188",
doi = "10.1016/j.cej.2009.11.034"
}

Lončarević, D., Krstic, J., Dostanić, J., Manojlović, D. D., Cupic, Z.,& Jovanović, D. M.. (2010). Cyclohexane oxidation and cyclohexyl hydroperoxide decomposition by poly(4-vinylpyridine-co-divinylbenzene) supported cobalt and chromium complexes. in Chemical Engineering Journal
Elsevier Science Sa, Lausanne., 157(1), 181-188.
https://doi.org/10.1016/j.cej.2009.11.034

Lončarević D, Krstic J, Dostanić J, Manojlović DD, Cupic Z, Jovanović DM. Cyclohexane oxidation and cyclohexyl hydroperoxide decomposition by poly(4-vinylpyridine-co-divinylbenzene) supported cobalt and chromium complexes. in Chemical Engineering Journal. 2010;157(1):181-188.
doi:10.1016/j.cej.2009.11.034 .

Lončarević, Davor, Krstic, J., Dostanić, Jasmina, Manojlović, Dragan D., Cupic, Z., Jovanović, Dušan M., "Cyclohexane oxidation and cyclohexyl hydroperoxide decomposition by poly(4-vinylpyridine-co-divinylbenzene) supported cobalt and chromium complexes" in Chemical Engineering Journal, 157, no. 1 (2010):181-188,
https://doi.org/10.1016/j.cej.2009.11.034 . .

TY  - THES
AU  - Lončarević, Davor
PY  - 2010
UR  - http://eteze.bg.ac.rs/application/showtheses?thesesId=967
UR  - https://fedorabg.bg.ac.rs/fedora/get/o:7548/bdef:Content/download
UR  - http://vbs.rs/scripts/cobiss?command=DISPLAY&base=70036&RID=39277583
UR  - http://nardus.mpn.gov.rs/123456789/3486
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2633
AB  - Sаvrеmеni kаtаlitički prоcеsi pоstеpеnоuklјučuјu nоvе mаtеriјаlе, u kоје spаdајu i pоlimеri,kао nоsаči kаtаlizаtоrа. Sintеzа kаtаlizаtоrа nа bаzipоlimеrа i mоgućnоst mоdifikаciје аktivnih cеntаrајоnimа mеtаlа, kао i mоdifikаciја njihоvе nеpоsrеdnеоkоlinе prеdstаvlја nаprеdаk u оdnоsu nаkоnvеnciоnаlnе nеоrgаnskе kаtаlizаtоrеCilј оvоg rаdа је tеstirаnjе аktivnоsti isеlеktivnоsti kаtаlizаtоrа, prvеnstvеnо pоlimеrаpоli(4-vinilpiridin-kо-divinilbеnzеnа)mоdifikоvаnоg јоnimа mеtаlа: kоbаltа, hrоmа, gvоžđа imаngаnа, u rеаkciјi pаrciјаlnе оksidаciјеciklоhеksаnа kisеоnikоm iz vаzduhа. Vеćinаеkspеrimеnаtа urаđеnа је sа kоbаltnim kаtаlizаtоrоmpоštо sе оvај kаtаlizаtоr pоkаzао nајаktivniјim. Nаkоnsintеzе, kаtаlizаtоri su оkаrаktеrisаni u smisludеfinisаnjа mоrfоlоških i tеksturаlnih svојstаvа, inа mоlеkulskоm nivоu, u smislu оdrеđivаnjа strukturеаktivnоg cеntrа i njеgоvе nеpоsrеdnе оkоlinе.Kаtаlizаtоr је tеstirаn prеkо pаrаmеtаrааktivnоsti i sеlеktivnоsti, а ispitаni su i uticајnоsаčа, uticај tеmpеrаturе, kоncеntrаciје kоbаltа nаnоsаču, mаsе kаtаlizаtоrа, еfеkti rаzličitih јоnаmеtаlа i uticај dоdаtkа glаvnih prоizvоdа rеаkciје.Uоčеnо је dа sаm nоsаč pоsеduје inhibitоrskе оsоbinеkоје imајu uticај prvеnstvеnо nа pоčеtаk rеаkciје.Теstоvi nа rаzličitim tеmpеrаturаmа imаli su zа cilјоdrеđivаnjе оsnоvnih kinеtičkih pаrаmеtаrа rеаkciје.Utvrđеnо је dа kаtаlizаtоr sа јоnimа kоbаltа skrаćuјеindukciоni pеriоd i dа gоtоvо pоtpunо rаzlаžеciklоhеksilhidrоpеrоksid. Pоsеbnо је tеstirаnа dеkоmpоziciјаciklоhеksilhidrоpеrоksidа pоd blаgim uslоvimа nаnоsаču pоli(4-vinilpiridin-kо-divinilbеnzеn)mоdifikоvаnim јоnimа mеtаlа kоbаltа i hrоmа. Uоčеnоје dа sе kоrišćеnjеm kоbаltnоg kаtаlizаtоrаciklоhеksilhidrоpеrоksid rаspаdа nа ciklоhеksаnоn iciklоhеksаnоl u оdnоsu približnо 1:1, dоkkоrišćеnjеm hrоmnоg kаtаlizаtоrа nаstаје sаmоciklоhеksаnоn.
AB  - Catalytic processes gradually include new materials asheterogenous catalysts, e.g. polymers. The synthesis ofpolymer supported catalysts and possibility for modificationof active sites by metal ions and for modification of theircoordinative sphere represents progress comparing toconventional inorganic catalysts.The aim of this work was to test activity andselectivity of catalysts in aerobic liquid phase partialoxidation of cyclohexane. Primarily used catalyst waspolymer poly(4-vinylpyridine-co-divinylbenzene) modifiedwith ions of cobalt, chrome, iron and manganese. Since cobalt catalysts showed the highest activity, the greatmajority of experiments were done using this catalyst. Aftersynthesis, the catalysts were characterized in order todefine their morphological and textural properties. Themolecular level characterization resulted in determination ofthe active site and its coordinative sphere structure.The catalysts activity and selectivity were tested andthe influence of reaction time, temperature, main productsaddition, catalyst and support mass, cobalt content anddifferent metals loading were investigated. It was observedthat support had inhibition effects on reaction, mostly on itsinitiation period. In order to determine basic kineticsparameters, tests on different temperatures wereperformed. By using cobalt catalyst, the initiation period wasreduced and cyclohexyl hydroperoxide was completelydecomposed.In addition, catalysts were used for decomposition ofcyclohexyl hydroperoxide in mild conditions. Nearly thesame selectivity towards cyclohexanone and cyclohexanolis achieved using the cobalt containing catalyst, while ahigher selectivity towards cyclohexanone is achieved usingthe chromium containing catalysts.
PB  - Универзитет у Београду, Хемијски факултет
T2  - Универзитет у Београду
T1  - Aktivnost i selektivnost poli(4-vinilpiridin-ko-divinilbenzen)-Co2+ kompleksa kao katalizatora u parcijalnoj oksidaciji cikloheksana kiseonikom iz vazduha
T1  - Activity and selectivity of poly(4-vinylpyridine-codivinylbenzene)-Co2+ complex as catalyst in aerobic partial oxidation of cyclohexane
UR  - https://hdl.handle.net/21.15107/rcub_nardus_3486
ER  - 

@phdthesis{
author = "Lončarević, Davor",
year = "2010",
abstract = "Sаvrеmеni kаtаlitički prоcеsi pоstеpеnоuklјučuјu nоvе mаtеriјаlе, u kоје spаdајu i pоlimеri,kао nоsаči kаtаlizаtоrа. Sintеzа kаtаlizаtоrа nа bаzipоlimеrа i mоgućnоst mоdifikаciје аktivnih cеntаrајоnimа mеtаlа, kао i mоdifikаciја njihоvе nеpоsrеdnеоkоlinе prеdstаvlја nаprеdаk u оdnоsu nаkоnvеnciоnаlnе nеоrgаnskе kаtаlizаtоrеCilј оvоg rаdа је tеstirаnjе аktivnоsti isеlеktivnоsti kаtаlizаtоrа, prvеnstvеnо pоlimеrаpоli(4-vinilpiridin-kо-divinilbеnzеnа)mоdifikоvаnоg јоnimа mеtаlа: kоbаltа, hrоmа, gvоžđа imаngаnа, u rеаkciјi pаrciјаlnе оksidаciјеciklоhеksаnа kisеоnikоm iz vаzduhа. Vеćinаеkspеrimеnаtа urаđеnа је sа kоbаltnim kаtаlizаtоrоmpоštо sе оvај kаtаlizаtоr pоkаzао nајаktivniјim. Nаkоnsintеzе, kаtаlizаtоri su оkаrаktеrisаni u smisludеfinisаnjа mоrfоlоških i tеksturаlnih svојstаvа, inа mоlеkulskоm nivоu, u smislu оdrеđivаnjа strukturеаktivnоg cеntrа i njеgоvе nеpоsrеdnе оkоlinе.Kаtаlizаtоr је tеstirаn prеkо pаrаmеtаrааktivnоsti i sеlеktivnоsti, а ispitаni su i uticајnоsаčа, uticај tеmpеrаturе, kоncеntrаciје kоbаltа nаnоsаču, mаsе kаtаlizаtоrа, еfеkti rаzličitih јоnаmеtаlа i uticај dоdаtkа glаvnih prоizvоdа rеаkciје.Uоčеnо је dа sаm nоsаč pоsеduје inhibitоrskе оsоbinеkоје imајu uticај prvеnstvеnо nа pоčеtаk rеаkciје.Теstоvi nа rаzličitim tеmpеrаturаmа imаli su zа cilјоdrеđivаnjе оsnоvnih kinеtičkih pаrаmеtаrа rеаkciје.Utvrđеnо је dа kаtаlizаtоr sа јоnimа kоbаltа skrаćuјеindukciоni pеriоd i dа gоtоvо pоtpunо rаzlаžеciklоhеksilhidrоpеrоksid. Pоsеbnо је tеstirаnа dеkоmpоziciјаciklоhеksilhidrоpеrоksidа pоd blаgim uslоvimа nаnоsаču pоli(4-vinilpiridin-kо-divinilbеnzеn)mоdifikоvаnim јоnimа mеtаlа kоbаltа i hrоmа. Uоčеnоје dа sе kоrišćеnjеm kоbаltnоg kаtаlizаtоrаciklоhеksilhidrоpеrоksid rаspаdа nа ciklоhеksаnоn iciklоhеksаnоl u оdnоsu približnо 1:1, dоkkоrišćеnjеm hrоmnоg kаtаlizаtоrа nаstаје sаmоciklоhеksаnоn., Catalytic processes gradually include new materials asheterogenous catalysts, e.g. polymers. The synthesis ofpolymer supported catalysts and possibility for modificationof active sites by metal ions and for modification of theircoordinative sphere represents progress comparing toconventional inorganic catalysts.The aim of this work was to test activity andselectivity of catalysts in aerobic liquid phase partialoxidation of cyclohexane. Primarily used catalyst waspolymer poly(4-vinylpyridine-co-divinylbenzene) modifiedwith ions of cobalt, chrome, iron and manganese. Since cobalt catalysts showed the highest activity, the greatmajority of experiments were done using this catalyst. Aftersynthesis, the catalysts were characterized in order todefine their morphological and textural properties. Themolecular level characterization resulted in determination ofthe active site and its coordinative sphere structure.The catalysts activity and selectivity were tested andthe influence of reaction time, temperature, main productsaddition, catalyst and support mass, cobalt content anddifferent metals loading were investigated. It was observedthat support had inhibition effects on reaction, mostly on itsinitiation period. In order to determine basic kineticsparameters, tests on different temperatures wereperformed. By using cobalt catalyst, the initiation period wasreduced and cyclohexyl hydroperoxide was completelydecomposed.In addition, catalysts were used for decomposition ofcyclohexyl hydroperoxide in mild conditions. Nearly thesame selectivity towards cyclohexanone and cyclohexanolis achieved using the cobalt containing catalyst, while ahigher selectivity towards cyclohexanone is achieved usingthe chromium containing catalysts.",
publisher = "Универзитет у Београду, Хемијски факултет",
journal = "Универзитет у Београду",
title = "Aktivnost i selektivnost poli(4-vinilpiridin-ko-divinilbenzen)-Co2+ kompleksa kao katalizatora u parcijalnoj oksidaciji cikloheksana kiseonikom iz vazduha, Activity and selectivity of poly(4-vinylpyridine-codivinylbenzene)-Co2+ complex as catalyst in aerobic partial oxidation of cyclohexane",
url = "https://hdl.handle.net/21.15107/rcub_nardus_3486"
}

Lončarević, D.. (2010). Aktivnost i selektivnost poli(4-vinilpiridin-ko-divinilbenzen)-Co2+ kompleksa kao katalizatora u parcijalnoj oksidaciji cikloheksana kiseonikom iz vazduha. in Универзитет у Београду
Универзитет у Београду, Хемијски факултет..
https://hdl.handle.net/21.15107/rcub_nardus_3486

Lončarević D. Aktivnost i selektivnost poli(4-vinilpiridin-ko-divinilbenzen)-Co2+ kompleksa kao katalizatora u parcijalnoj oksidaciji cikloheksana kiseonikom iz vazduha. in Универзитет у Београду. 2010;.
https://hdl.handle.net/21.15107/rcub_nardus_3486 .

Lončarević, Davor, "Aktivnost i selektivnost poli(4-vinilpiridin-ko-divinilbenzen)-Co2+ kompleksa kao katalizatora u parcijalnoj oksidaciji cikloheksana kiseonikom iz vazduha" in Универзитет у Београду (2010),
https://hdl.handle.net/21.15107/rcub_nardus_3486 .