TY  - CONF
AU  - Milenković, Maja
AU  - Stanisavljev, Dragomir
AU  - Mudrinić, Tihana
AU  - Vuković, Milica
PY  - 2010
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/6810
AB  - The kinetics of the complex reaction between I– and H2O2 in acid media is investigated. The particular attention is focused on the determination of the rate
constant of the reaction between HIO and H2O2 involved in investigated complex
process. The examination of the whole kinetics was performed by monitoring
evolution of O2 pressure, I3– and I– concentrations. We modeled behavior of
experimentally followed components based on Liebhafsky research. Our
preliminary results suggest a significantly higher rate constant of the reaction
between HIO and H2O2 from those proposed in the literature.
PB  - Society of Physical Chemists of Serbia
C3  - Proceedings - 10th International Conference on Fundamental and Applied Aspects of Physical Chemistry, Physical Chemistry 2010, 21-24 September 2010, Belgrade, Serbia
T1  - The Kinetics of Reaction between Iodide and Hydrogen Peroxide in Acid Solution
SP  - 242
EP  - 244
UR  - https://hdl.handle.net/21.15107/rcub_cer_6810
ER  - 

@conference{
author = "Milenković, Maja and Stanisavljev, Dragomir and Mudrinić, Tihana and Vuković, Milica",
year = "2010",
abstract = "The kinetics of the complex reaction between I– and H2O2 in acid media is investigated. The particular attention is focused on the determination of the rate
constant of the reaction between HIO and H2O2 involved in investigated complex
process. The examination of the whole kinetics was performed by monitoring
evolution of O2 pressure, I3– and I– concentrations. We modeled behavior of
experimentally followed components based on Liebhafsky research. Our
preliminary results suggest a significantly higher rate constant of the reaction
between HIO and H2O2 from those proposed in the literature.",
publisher = "Society of Physical Chemists of Serbia",
journal = "Proceedings - 10th International Conference on Fundamental and Applied Aspects of Physical Chemistry, Physical Chemistry 2010, 21-24 September 2010, Belgrade, Serbia",
title = "The Kinetics of Reaction between Iodide and Hydrogen Peroxide in Acid Solution",
pages = "242-244",
url = "https://hdl.handle.net/21.15107/rcub_cer_6810"
}

Milenković, M., Stanisavljev, D., Mudrinić, T.,& Vuković, M.. (2010). The Kinetics of Reaction between Iodide and Hydrogen Peroxide in Acid Solution. in Proceedings - 10th International Conference on Fundamental and Applied Aspects of Physical Chemistry, Physical Chemistry 2010, 21-24 September 2010, Belgrade, Serbia
Society of Physical Chemists of Serbia., 242-244.
https://hdl.handle.net/21.15107/rcub_cer_6810

Milenković M, Stanisavljev D, Mudrinić T, Vuković M. The Kinetics of Reaction between Iodide and Hydrogen Peroxide in Acid Solution. in Proceedings - 10th International Conference on Fundamental and Applied Aspects of Physical Chemistry, Physical Chemistry 2010, 21-24 September 2010, Belgrade, Serbia. 2010;:242-244.
https://hdl.handle.net/21.15107/rcub_cer_6810 .

Milenković, Maja, Stanisavljev, Dragomir, Mudrinić, Tihana, Vuković, Milica, "The Kinetics of Reaction between Iodide and Hydrogen Peroxide in Acid Solution" in Proceedings - 10th International Conference on Fundamental and Applied Aspects of Physical Chemistry, Physical Chemistry 2010, 21-24 September 2010, Belgrade, Serbia (2010):242-244,
https://hdl.handle.net/21.15107/rcub_cer_6810 .

TY  - JOUR
AU  - Jovanović, Bratislav Ž.
AU  - Mišić-Vuković, Milica M.
AU  - Marinković, Aleksandar D.
AU  - Vajs, Vlatka
PY  - 1999
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2813
AB  - 13 C chemical shifts of the azomethine carbon atom for N-(substituted phenyl)pyridine-4-aldimines, 4-Py-CH=N-C 6 H 4 -X, X having a wide range of substituent effects, have been determined in CDCl 3 solution. Exceptionally good Hammett correlations of 13 C NMR chemical shifts of azomethine carbons with electrophilic substituent constants σ + points out to a strong resonance interaction of substituents on the aniline ring with the azomethine carbon atom of the investigated imines. The increased demand for elections in the investigated system is being compared with that of the N- benzylidenaniline. The mode of transmission of substituent effects, both inductive and resonance, both systems, is discussed.
PB  - Elsevier
T2  - Journal of Molecular Structure
T1  - Effect of substituents on the 13 C chemical shifts of the azomethine carbon atom of N-(phenyl substituted) pyridine-4-aldimines
VL  - 482-483
SP  - 375
EP  - 378
DO  - 10.1016/S0022-2860(98)00860-6
ER  - 

@article{
author = "Jovanović, Bratislav Ž. and Mišić-Vuković, Milica M. and Marinković, Aleksandar D. and Vajs, Vlatka",
year = "1999",
abstract = "13 C chemical shifts of the azomethine carbon atom for N-(substituted phenyl)pyridine-4-aldimines, 4-Py-CH=N-C 6 H 4 -X, X having a wide range of substituent effects, have been determined in CDCl 3 solution. Exceptionally good Hammett correlations of 13 C NMR chemical shifts of azomethine carbons with electrophilic substituent constants σ + points out to a strong resonance interaction of substituents on the aniline ring with the azomethine carbon atom of the investigated imines. The increased demand for elections in the investigated system is being compared with that of the N- benzylidenaniline. The mode of transmission of substituent effects, both inductive and resonance, both systems, is discussed.",
publisher = "Elsevier",
journal = "Journal of Molecular Structure",
title = "Effect of substituents on the 13 C chemical shifts of the azomethine carbon atom of N-(phenyl substituted) pyridine-4-aldimines",
volume = "482-483",
pages = "375-378",
doi = "10.1016/S0022-2860(98)00860-6"
}

Jovanović, B. Ž., Mišić-Vuković, M. M., Marinković, A. D.,& Vajs, V.. (1999). Effect of substituents on the 13 C chemical shifts of the azomethine carbon atom of N-(phenyl substituted) pyridine-4-aldimines. in Journal of Molecular Structure
Elsevier., 482-483, 375-378.
https://doi.org/10.1016/S0022-2860(98)00860-6

Jovanović BŽ, Mišić-Vuković MM, Marinković AD, Vajs V. Effect of substituents on the 13 C chemical shifts of the azomethine carbon atom of N-(phenyl substituted) pyridine-4-aldimines. in Journal of Molecular Structure. 1999;482-483:375-378.
doi:10.1016/S0022-2860(98)00860-6 .

Jovanović, Bratislav Ž., Mišić-Vuković, Milica M., Marinković, Aleksandar D., Vajs, Vlatka, "Effect of substituents on the 13 C chemical shifts of the azomethine carbon atom of N-(phenyl substituted) pyridine-4-aldimines" in Journal of Molecular Structure, 482-483 (1999):375-378,
https://doi.org/10.1016/S0022-2860(98)00860-6 . .

TY  - JOUR
AU  - Jovanović, Bratislav Ž.
AU  - Mišić-Vuković, Milica M.
AU  - Vajs, Vlatka
AU  - Čanadi, J. J.
PY  - 1992
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2789
AB  - The 13C N.M.R. spectra of some substituted α-phenylpyridylacrylic acids, α-phenyl, α-(3-pyrydyl) and α-(3-pyrydyl-N-oxide) cinnamic acids were determined in deuterated dimethyl sulfoxide (d6-DMSO). It has been shown that the subsitutent chemical shifts (SCS) for Cβatom ethylenic bond of the examined compounds correlated linearely with the summ of the corresponding substituent constants in the both rings (σx + σY). This correlation was interpreted as evidence that the electronic effects of both substituents are involved in conjugated aromatic system. © 1992.
PB  - Elsevier Science Publishers B.V.
T2  - Journal of Molecular Structure
T1  - Substituent efects on the carbon-13 chemical shifts in α-phenylpyridylacrylic acids
VL  - 267
IS  - C
SP  - 411
EP  - 414
DO  - 10.1016/0022-2860(92)87065-4
ER  - 

@article{
author = "Jovanović, Bratislav Ž. and Mišić-Vuković, Milica M. and Vajs, Vlatka and Čanadi, J. J.",
year = "1992",
abstract = "The 13C N.M.R. spectra of some substituted α-phenylpyridylacrylic acids, α-phenyl, α-(3-pyrydyl) and α-(3-pyrydyl-N-oxide) cinnamic acids were determined in deuterated dimethyl sulfoxide (d6-DMSO). It has been shown that the subsitutent chemical shifts (SCS) for Cβatom ethylenic bond of the examined compounds correlated linearely with the summ of the corresponding substituent constants in the both rings (σx + σY). This correlation was interpreted as evidence that the electronic effects of both substituents are involved in conjugated aromatic system. © 1992.",
publisher = "Elsevier Science Publishers B.V.",
journal = "Journal of Molecular Structure",
title = "Substituent efects on the carbon-13 chemical shifts in α-phenylpyridylacrylic acids",
volume = "267",
number = "C",
pages = "411-414",
doi = "10.1016/0022-2860(92)87065-4"
}

Jovanović, B. Ž., Mišić-Vuković, M. M., Vajs, V.,& Čanadi, J. J.. (1992). Substituent efects on the carbon-13 chemical shifts in α-phenylpyridylacrylic acids. in Journal of Molecular Structure
Elsevier Science Publishers B.V.., 267(C), 411-414.
https://doi.org/10.1016/0022-2860(92)87065-4

Jovanović BŽ, Mišić-Vuković MM, Vajs V, Čanadi JJ. Substituent efects on the carbon-13 chemical shifts in α-phenylpyridylacrylic acids. in Journal of Molecular Structure. 1992;267(C):411-414.
doi:10.1016/0022-2860(92)87065-4 .

Jovanović, Bratislav Ž., Mišić-Vuković, Milica M., Vajs, Vlatka, Čanadi, J. J., "Substituent efects on the carbon-13 chemical shifts in α-phenylpyridylacrylic acids" in Journal of Molecular Structure, 267, no. C (1992):411-414,
https://doi.org/10.1016/0022-2860(92)87065-4 . .

TY  - JOUR
AU  - Milutinović Nikolić, Aleksandra
AU  - Mišić-Vuković, Milica M.
PY  - 1991
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4137
AB  - A series of eight alpha amylases (EC 3.2.1.1) of known primary structure were investigated using the Informational Spectrum Method (ISM) for the purpose of predicting new enzymes with increased efficiency.
AB  - Niz od 8 α-amilaza (1,4-α-D-glukan-glukano -hidrolaze, EC 3.2.1.1) poznate primarne strukture ispitivano je metodom informacionih spektara (ISM) , s ciljem da se predlože novi enzimi veće efikasnosti. Pomoću ISM-a transformisana je primarna struktura enzima u niz brojeva, a zatim je bilo moguće dobiti i uporediti originalne spektre. Korišćenjem multi-spektralne funkcije utvrđen je samo jedan zajednički, dobro definisan pik. Frekvenca ovog pika predstavlja karakterističnu frekvencu svih ispitivanih amilaza. Postoji zavisnost između vrednosti amplitude na karakterističnoj frekvenciji i aktivnosti biomolekula. Daljom matematičkom obradom, metoda je dala predlog za minimalne promene u strukturi prirodnog proizvoda kojima se omogućava povećana efikasnost enzima. Ove minimalne promene moguće je izvesti najjednostavnijom metodom genetskog inženjerstva - metodom tačkaste mutacije. Mutacije su predložene za α-amilaze iz sledećih izvora: Aspergillus oryzae, Bacillus arnyloliquefaciens i ječam.
PB  - Serbian Chemical Society / Srpsko hemijsko društvo
T2  - Journal of the Serbian Chemical Society
T1  - Informational spectrum method applied to the investigation of the enzymatic activity of different alpha amylases
T1  - Primena metode informacionih spektara u ispitivanju enzimatskih različitih alfa amilaza
VL  - 56
IS  - 10
SP  - 567
EP  - 579
UR  - https://hdl.handle.net/21.15107/rcub_cer_4137
ER  - 

@article{
author = "Milutinović Nikolić, Aleksandra and Mišić-Vuković, Milica M.",
year = "1991",
abstract = "A series of eight alpha amylases (EC 3.2.1.1) of known primary structure were investigated using the Informational Spectrum Method (ISM) for the purpose of predicting new enzymes with increased efficiency., Niz od 8 α-amilaza (1,4-α-D-glukan-glukano -hidrolaze, EC 3.2.1.1) poznate primarne strukture ispitivano je metodom informacionih spektara (ISM) , s ciljem da se predlože novi enzimi veće efikasnosti. Pomoću ISM-a transformisana je primarna struktura enzima u niz brojeva, a zatim je bilo moguće dobiti i uporediti originalne spektre. Korišćenjem multi-spektralne funkcije utvrđen je samo jedan zajednički, dobro definisan pik. Frekvenca ovog pika predstavlja karakterističnu frekvencu svih ispitivanih amilaza. Postoji zavisnost između vrednosti amplitude na karakterističnoj frekvenciji i aktivnosti biomolekula. Daljom matematičkom obradom, metoda je dala predlog za minimalne promene u strukturi prirodnog proizvoda kojima se omogućava povećana efikasnost enzima. Ove minimalne promene moguće je izvesti najjednostavnijom metodom genetskog inženjerstva - metodom tačkaste mutacije. Mutacije su predložene za α-amilaze iz sledećih izvora: Aspergillus oryzae, Bacillus arnyloliquefaciens i ječam.",
publisher = "Serbian Chemical Society / Srpsko hemijsko društvo",
journal = "Journal of the Serbian Chemical Society",
title = "Informational spectrum method applied to the investigation of the enzymatic activity of different alpha amylases, Primena metode informacionih spektara u ispitivanju enzimatskih različitih alfa amilaza",
volume = "56",
number = "10",
pages = "567-579",
url = "https://hdl.handle.net/21.15107/rcub_cer_4137"
}

Milutinović Nikolić, A.,& Mišić-Vuković, M. M.. (1991). Informational spectrum method applied to the investigation of the enzymatic activity of different alpha amylases. in Journal of the Serbian Chemical Society
Serbian Chemical Society / Srpsko hemijsko društvo., 56(10), 567-579.
https://hdl.handle.net/21.15107/rcub_cer_4137

Milutinović Nikolić A, Mišić-Vuković MM. Informational spectrum method applied to the investigation of the enzymatic activity of different alpha amylases. in Journal of the Serbian Chemical Society. 1991;56(10):567-579.
https://hdl.handle.net/21.15107/rcub_cer_4137 .

Milutinović Nikolić, Aleksandra, Mišić-Vuković, Milica M., "Informational spectrum method applied to the investigation of the enzymatic activity of different alpha amylases" in Journal of the Serbian Chemical Society, 56, no. 10 (1991):567-579,
https://hdl.handle.net/21.15107/rcub_cer_4137 .