Olga N. Pestova
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Olga N. Pestova has a total of 38 co-authors. Here are the top co-authors by number of shared publications:
- Valeriia Baranauskaite
St. Petersburg State University
6 shared publications - Mikhail Yu. Skripkin
Institute of chemistry, Saint Petersburg State University, 7/9 Universitetskaya Emb., Saint Petersburg 199034, Russia
4 shared publications - Nikita A. Bogachev
Institute of chemistry, Saint Petersburg State University, 7/9 Universitetskaya Emb., Saint Petersburg 199034, Russia
3 shared publications - Vasilii D. Khripun
Chemistry Institute, Federal University of Mato Grosso do Sul, Campo Grande 79079-900, MS, Brazil
3 shared publications - Andrey S. Mereshchenko
Institute of Chemistry, Saint Petersburg State University, 26 Universitetskii pr, St. Petersburg 198504, Russia
2 shared publications Andrey Yu. Efimov
St. Petersburg State University
2 shared publications
Latest Publications
- 26 December 2024
- Published by American Chemical Society (ACS) in The Journal of Physical Chemistry B
- Vol. 129 (1) , 153-161
Thermodynamic Description of Oxotransfer Processes Involving Molybdenum and Tungsten Enzyme Models: DFT Calculations and Calorimetry
The enthalpy of the oxotransfer reaction of [Bu4N]2[WO2(mnt)2] (where mnt2- is maleonitriledithiolate) with PPh3 in an inert atmosphere in an acetonitrile solution was determined by calorimetry. The obtained enthalpy value (-93 ± 5) kJ mol-1 differs from the enthalpy value of the reaction carried out by us earlier under aerobic conditions by (16 ± 9) kJ mol-1. The obtained results indicate the participation of atmospheric oxygen in the catalytic process. DFT calculations of the structures [MOx(LL)2]2- (where M = Mo or W, x = 1 or 2, and LL is dithiolene ligand) were carried out. DFT calculations of the thermodynamic potential values for the oxygen transfer reaction in the system [MIVO2(LL)2]2- - [MVIO(LL)2]2- were also carried out. It was shown that the determining contribution to these processes is made by the enthalpy changes. The enthalpies of these processes depend on the donor-acceptor characteristics of the dithiolene ligands. In the case of good acceptors, the oxidation process is more exothermic. The opposite picture is observed for the reduction processes of the complex. The M═O bond length can be used as a quantitative criterion for donor-acceptor properties of the ligands. Also, for molybdenum complexes, reduction processes are more favorable, while for tungsten complexes, oxidation processes are more favorable. The calculations agree well with experimental data that prove the validity of the model used for DFT calculations.
- 26 December 2024
- Published by American Chemical Society (ACS) in The Journal of Physical Chemistry B
- Vol. 129 (1) , 153-161
Thermodynamic Description of Oxotransfer Processes Involving Molybdenum and Tungsten Enzyme Models: DFT Calculations and Calorimetry
The enthalpy of the oxotransfer reaction of [Bu4N]2[WO2(mnt)2] (where mnt2- is maleonitriledithiolate) with PPh3 in an inert atmosphere in an acetonitrile solution was determined by calorimetry. The obtained enthalpy value (-93 ± 5) kJ mol-1 differs from the enthalpy value of the reaction carried out by us earlier under aerobic conditions by (16 ± 9) kJ mol-1. The obtained results indicate the participation of atmospheric oxygen in the catalytic process. DFT calculations of the structures [MOx(LL)2]2- (where M = Mo or W, x = 1 or 2, and LL is dithiolene ligand) were carried out. DFT calculations of the thermodynamic potential values for the oxygen transfer reaction in the system [MIVO2(LL)2]2- - [MVIO(LL)2]2- were also carried out. It was shown that the determining contribution to these processes is made by the enthalpy changes. The enthalpies of these processes depend on the donor-acceptor characteristics of the dithiolene ligands. In the case of good acceptors, the oxidation process is more exothermic. The opposite picture is observed for the reduction processes of the complex. The M═O bond length can be used as a quantitative criterion for donor-acceptor properties of the ligands. Also, for molybdenum complexes, reduction processes are more favorable, while for tungsten complexes, oxidation processes are more favorable. The calculations agree well with experimental data that prove the validity of the model used for DFT calculations.
- 12 April 2024
- Published by Springer Nature in Journal of Thermal Analysis and Calorimetry
- Vol. 149 (10) , 4771-4781
Oxidation of PPh3 by oxygen catalyzed by biomimetic tungsten complex: oxo-transfer process thermodynamics
- 12 April 2024
- Published by Springer Nature in Journal of Thermal Analysis and Calorimetry
- Vol. 149 (10) , 4771-4781
Oxidation of PPh3 by oxygen catalyzed by biomimetic tungsten complex: oxo-transfer process thermodynamics
- Open Access
- 24 December 2023
- Published by IFHAN in International Journal of Corrosion and Scale Inhibition
- Vol. 12 (4) , 2066-2079
Titanium oxo-hydroxo complexes as precursors of protective oxide films on the surface of titanium alloys in high-temperature water
- 24 December 2023
- Published by IFHAN in International Journal of Corrosion and Scale Inhibition
- Vol. 12 (4) , 2066-2079
Open AccessTitanium oxo-hydroxo complexes as precursors of protective oxide films on the surface of titanium alloys in high-temperature water
- 1 December 2023
- Published by Pleiades Publishing Ltd in Russian Journal of General Chemistry
- Vol. 93 (12) , 3135-3142
Complexation of Lanthanide Ions with Citric Acid in Aqueous Solutions
The stability constants of triply charged lanthanide ion complexes with citric acid of 1 : 2 stoichiometry were measured by potentiometric titration in a wide pH range, and the relationship between the constants and the lanthanide type was analyzed. A mathematical model for the equilibrium in studied solutions was proposed.
- 1 December 2023
- Published by Pleiades Publishing Ltd in Russian Journal of General Chemistry
- Vol. 93 (12) , 3135-3142
Complexation of Lanthanide Ions with Citric Acid in Aqueous Solutions
The stability constants of triply charged lanthanide ion complexes with citric acid of 1 : 2 stoichiometry were measured by potentiometric titration in a wide pH range, and the relationship between the constants and the lanthanide type was analyzed. A mathematical model for the equilibrium in studied solutions was proposed.
- Open Access
Thermodynamic Description of Dilution and Dissolution Processes in the MgCl2−CsCl−H2O Ternary System
Thermodynamic data on the properties of the water-based electrolyte systems are very valuable for fundamental physical chemistry and for industrial applications. The missing data both on the dilution and dissolution enthalpies for the ternary CsCl−MgCl2−H2O mixed electrolyte system were investigated by means of the calorimetry method. The dilution calorimetry was performed at 298 for the set of solutions from diluted to concentrated at constant ratio Cs+/Mg2+. The relative partial molar enthalpies, ideal, total, and excess ones were calculated. By means of the dissolution calorimetry, the standard enthalpies of formation, the enthalpies, and entropies for the double salt formation from simple salts were evaluated. The results obtained indicate that entropy as the major factor affecting the formation of the joint compound, both in the liquid and solid phases. These data can be implemented in thermodynamic databases and allow for accurate thermodynamic calculations for the salts extraction from natural water sources and for its possible application as thermochemical energy storage.Open AccessThermodynamic Description of Dilution and Dissolution Processes in the MgCl2−CsCl−H2O Ternary System
Thermodynamic data on the properties of the water-based electrolyte systems are very valuable for fundamental physical chemistry and for industrial applications. The missing data both on the dilution and dissolution enthalpies for the ternary CsCl−MgCl2−H2O mixed electrolyte system were investigated by means of the calorimetry method. The dilution calorimetry was performed at 298 for the set of solutions from diluted to concentrated at constant ratio Cs+/Mg2+. The relative partial molar enthalpies, ideal, total, and excess ones were calculated. By means of the dissolution calorimetry, the standard enthalpies of formation, the enthalpies, and entropies for the double salt formation from simple salts were evaluated. The results obtained indicate that entropy as the major factor affecting the formation of the joint compound, both in the liquid and solid phases. These data can be implemented in thermodynamic databases and allow for accurate thermodynamic calculations for the salts extraction from natural water sources and for its possible application as thermochemical energy storage. - 9 October 2019
- Published by Royal Society of Chemistry (RSC) in Physical Chemistry Chemical Physics
- Vol. 21 (41) , 22895-22901
Local dynamics in LiCl–CsCl–D2O water-in-salt solutions according to NMR relaxation
The main purpose of this study is to investigate the local structure and dynamics in ‘water-in-salt’ solutions, namely the ternary concentrated LiCl–CsCl–D2O electrolytes.
- 9 October 2019
- Published by Royal Society of Chemistry (RSC) in Physical Chemistry Chemical Physics
- Vol. 21 (41) , 22895-22901
Local dynamics in LiCl–CsCl–D2O water-in-salt solutions according to NMR relaxation
The main purpose of this study is to investigate the local structure and dynamics in ‘water-in-salt’ solutions, namely the ternary concentrated LiCl–CsCl–D2O electrolytes.
- 1 June 2019
- Published by Pleiades Publishing Ltd in Russian Journal of General Chemistry
- Vol. 89 (6) , 1085-1101
Influence of Interactions in Solutions on the Solid Phase Formation in Ternary Water-Salt Systems
- 1 June 2019
- Published by Pleiades Publishing Ltd in Russian Journal of General Chemistry
- Vol. 89 (6) , 1085-1101
Influence of Interactions in Solutions on the Solid Phase Formation in Ternary Water-Salt Systems
- 1 March 2018
- Published by Pleiades Publishing Ltd in Russian Journal of General Chemistry
- Vol. 88 (3) , 596-597
Energy Characteristics of Lithium–Cesium Binary Chloride Dissolution in Water
Enthalpies of dissolution of the binary salt LiCl·3CsCl·4H2O and dry mixtures of lithium and cesium chlorides in the molar ratio 1: 3 were measured by the calorimetry method. The value of the mutual...
- 1 March 2018
- Published by Pleiades Publishing Ltd in Russian Journal of General Chemistry
- Vol. 88 (3) , 596-597
Energy Characteristics of Lithium–Cesium Binary Chloride Dissolution in Water
Enthalpies of dissolution of the binary salt LiCl·3CsCl·4H2O and dry mixtures of lithium and cesium chlorides in the molar ratio 1: 3 were measured by the calorimetry method. The value of the mutual...
- 15 September 2017
- Published by Springer Nature in Journal of Solution Chemistry
- Vol. 46 (9-10) , 1854-1870
Structural Inhomogeneity in Electrolyte Solutions: The Calcium Perchlorate–Water System
- 15 September 2017
- Published by Springer Nature in Journal of Solution Chemistry
- Vol. 46 (9-10) , 1854-1870
Structural Inhomogeneity in Electrolyte Solutions: The Calcium Perchlorate–Water System
- 1 April 2016
- Published by Pleiades Publishing Ltd in Russian Journal of General Chemistry
- Vol. 86 (4) , 767-770
Formation of binary salts in the system LiCl–CsCl–H2O
In the ternary system LiCl–CsCl–HO the binary salt LiCl·2CsCl·4HO was formed. Its structure was proved by the X-ray structural analysis. The binary compound formed in the aqueous solution by the structurally-forced insertion mechanism.
- 1 April 2016
- Published by Pleiades Publishing Ltd in Russian Journal of General Chemistry
- Vol. 86 (4) , 767-770
Formation of binary salts in the system LiCl–CsCl–H2O
In the ternary system LiCl–CsCl–HO the binary salt LiCl·2CsCl·4HO was formed. Its structure was proved by the X-ray structural analysis. The binary compound formed in the aqueous solution by the structurally-forced insertion mechanism.