Natalia Tarasova
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Natalia Tarasova has a total of 48 co-authors. Here are the top co-authors by number of shared publications:
- Alexey Zanin
Dmitry Mendeleev University of Chemical Technology of Russia, UNESCO Chair in Green Chemistry for Sustainable Development, Moscow, Russia
8 shared publications - Efrem Krivoborodov
D. Mendeleev University of Chemical Technology of Russia , 125047 , Moscow , Russia
3 shared publications - Yaroslav O. Mezhuev
Nesmeyanov Institute of Organoelement Compounds of the Russian Academy of Sciences, Moscow, Russia
3 shared publications Anatoly Ivanov
CJSC InTech, Novovoronezh, Russia
2 shared publications- Anna S. Makarova
Mendeleev University of Chemical Technology of Russia
2 shared publications - Boris G. Ershov
Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences, Leninsky pr. 31-4, 119071 Moscow, Russia
2 shared publications
Latest Publications
- 4 August 2025
- Published by Springer Nature in Journal of Solution Chemistry
- Vol. 55 (1) , 130-137
The Influence of the Composition of Aqueous Solutions as a Reaction Medium on the Parameters of Electron Beam Polymerization of Elemental Phosphorus
- 4 August 2025
- Published by Springer Nature in Journal of Solution Chemistry
- Vol. 55 (1) , 130-137
The Influence of the Composition of Aqueous Solutions as a Reaction Medium on the Parameters of Electron Beam Polymerization of Elemental Phosphorus
- 1 February 2023
- Published by Springer Nature in Russian Chemical Bulletin
- Vol. 72 (2) , 415-424
Nucleophilic activation of the sulfur S8 cyclic form as a green chemistry tool
- 1 February 2023
- Published by Springer Nature in Russian Chemical Bulletin
- Vol. 72 (2) , 415-424
Nucleophilic activation of the sulfur S8 cyclic form as a green chemistry tool
- Open Access
Formation of Hydrogels Based on a Copolymer of N-Vinyl-2-pyrrolidone and Glycidyl Methacrylate in the Presence of the Reaction Product of 1,3-Dimethylmidazolium Dimethylphosphate and Elemental Sulfur
The aim of the study is to search for a reaction that provides the possibility of tandem “one-pot” formation of polymer networks during radical copolymerization of N-vinyl-2-pyrrolidone and glycidyl methacrylate. It was shown that the addition of recently synthesized 1,3-dimethylimidazolium (phosphonooxy-)oligosulfanide makes it possible to obtain a cross-linked copolymer in one stage as a result of radical copolymerization of N-vinyl-2-pyrrolidone and glycidyl methacrylate with a molar ratio of monomers less than 1.4. The structure of the copolymerization products of N-vinyl-2-pyrroldione and glycidyl methacrylate formed in the presence of 1,3-dimethylimidazolium (phosphonooxy-)oligosulfanide was characterized by 1H NMR, FTIR and MALDI spectroscopy. 1H NMR spectroscopy revealed an interaction under moderate heating between glycidyl methacrylate and 1,3-dimethylimidazolium (phosphonooxy-)oligosulfanide, accompanied by the formation of a mixture of unsaturated products of complex structure, presumably acting as crosslinking agents. It is shown that when the molar ratio of N-vinyl-2-pyrroldione/glycidyl methacrylate comonomers is 0.89, a densely crosslinked copolymer is formed, capable of limited swelling in water with a velocity constant of 5.06 × 10−2 min−1 and an equilibrium degree of swelling of about 227%.
Open AccessFormation of Hydrogels Based on a Copolymer of N-Vinyl-2-pyrrolidone and Glycidyl Methacrylate in the Presence of the Reaction Product of 1,3-Dimethylmidazolium Dimethylphosphate and Elemental Sulfur
The aim of the study is to search for a reaction that provides the possibility of tandem “one-pot” formation of polymer networks during radical copolymerization of N-vinyl-2-pyrrolidone and glycidyl methacrylate. It was shown that the addition of recently synthesized 1,3-dimethylimidazolium (phosphonooxy-)oligosulfanide makes it possible to obtain a cross-linked copolymer in one stage as a result of radical copolymerization of N-vinyl-2-pyrrolidone and glycidyl methacrylate with a molar ratio of monomers less than 1.4. The structure of the copolymerization products of N-vinyl-2-pyrroldione and glycidyl methacrylate formed in the presence of 1,3-dimethylimidazolium (phosphonooxy-)oligosulfanide was characterized by 1H NMR, FTIR and MALDI spectroscopy. 1H NMR spectroscopy revealed an interaction under moderate heating between glycidyl methacrylate and 1,3-dimethylimidazolium (phosphonooxy-)oligosulfanide, accompanied by the formation of a mixture of unsaturated products of complex structure, presumably acting as crosslinking agents. It is shown that when the molar ratio of N-vinyl-2-pyrroldione/glycidyl methacrylate comonomers is 0.89, a densely crosslinked copolymer is formed, capable of limited swelling in water with a velocity constant of 5.06 × 10−2 min−1 and an equilibrium degree of swelling of about 227%.
- Open Access
- 16 January 2022
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 23 (2) , 949
Photochemical Synthesis of Silver Hydrosol Stabilized by Carbonate Ions and Study of Its Bactericidal Impact on Escherichia coli: Direct and Indirect Effects
The great attention paid to silver nanoparticles is largely related to their antibacterial and antiviral effects and their possible use as efficient biocidal agents. Silver nanoparticles are being widely introduced into various areas of life, including industry, medicine, and agriculture. This leads to their spreading and entering the environment, which generates the potential risk of toxic effect on humans and other biological organisms. Proposed paper describes the preparation of silver hydrosols containing spherical metal nanoparticles by photochemical reduction of Ag+ ions with oxalate ions. In deaerated solutions, this gives ~10 nm particles, while in aerated solutions, ~20 nm particles with inclusion of the oxide Ag2O are obtained. Nanoparticles inhibit the bacterium Escherichia coli and suppress the cell growth at concentrations of ~1 × 10−6–1 × 10−4 mol L−1. Silver particles cause the loss of pili and deformation and destruction of cell membranes. A mechanism of antibacterial action was proposed, taking into account indirect suppressing action of Ag+ ions released upon the oxidative metal dissolution and direct (contact) action of nanoparticles on bacterial cells, resulting in a change in the shape and destruction of the bacteria.
- 16 January 2022
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 23 (2) , 949
Open AccessPhotochemical Synthesis of Silver Hydrosol Stabilized by Carbonate Ions and Study of Its Bactericidal Impact on Escherichia coli: Direct and Indirect Effects
The great attention paid to silver nanoparticles is largely related to their antibacterial and antiviral effects and their possible use as efficient biocidal agents. Silver nanoparticles are being widely introduced into various areas of life, including industry, medicine, and agriculture. This leads to their spreading and entering the environment, which generates the potential risk of toxic effect on humans and other biological organisms. Proposed paper describes the preparation of silver hydrosols containing spherical metal nanoparticles by photochemical reduction of Ag+ ions with oxalate ions. In deaerated solutions, this gives ~10 nm particles, while in aerated solutions, ~20 nm particles with inclusion of the oxide Ag2O are obtained. Nanoparticles inhibit the bacterium Escherichia coli and suppress the cell growth at concentrations of ~1 × 10−6–1 × 10−4 mol L−1. Silver particles cause the loss of pili and deformation and destruction of cell membranes. A mechanism of antibacterial action was proposed, taking into account indirect suppressing action of Ag+ ions released upon the oxidative metal dissolution and direct (contact) action of nanoparticles on bacterial cells, resulting in a change in the shape and destruction of the bacteria.
- 2 December 2021
- Published by Taylor & Francis in Phosphorus, Sulfur, and Silicon and the Related Elements
- Vol. 197 (5-6) , 608-609
New approaches to the synthesis of modified red phosphorus under the high-energy radiation
In comparison with white phosphorus, the toxicity of red phosphorus is thousands times smaller. Therefore, red phosphorus is the main modification produced and consumed by industry. Productivity, quality and product range depend on the efficiency of the technological system, on the possibility of modernizing production by introducing new progressive and environmentally friendly technologies using modern equipment. Development of a technological project for the production of red phosphorus is an urgent issue, which is the goal and the task of the research. The article presents the results of the synthesis of phosphorus-containing polymers from the white phosphorus, carried out under the influence of a beam of accelerated electrons. Graphical Abstract
- 2 December 2021
- Published by Taylor & Francis in Phosphorus, Sulfur, and Silicon and the Related Elements
- Vol. 197 (5-6) , 608-609
New approaches to the synthesis of modified red phosphorus under the high-energy radiation
In comparison with white phosphorus, the toxicity of red phosphorus is thousands times smaller. Therefore, red phosphorus is the main modification produced and consumed by industry. Productivity, quality and product range depend on the efficiency of the technological system, on the possibility of modernizing production by introducing new progressive and environmentally friendly technologies using modern equipment. Development of a technological project for the production of red phosphorus is an urgent issue, which is the goal and the task of the research. The article presents the results of the synthesis of phosphorus-containing polymers from the white phosphorus, carried out under the influence of a beam of accelerated electrons. Graphical Abstract
- 1 December 2021
- Published by Springer Nature in Macromolecular Research
- Vol. 29 (12) , 847-850
Anionic Polymerization of Ethyl 2-Cyanoacrylate Initiated by 1,3-Dimethylimidazolium (phosphonooxy-)oligosulfanide
- 1 December 2021
- Published by Springer Nature in Macromolecular Research
- Vol. 29 (12) , 847-850
Anionic Polymerization of Ethyl 2-Cyanoacrylate Initiated by 1,3-Dimethylimidazolium (phosphonooxy-)oligosulfanide
- Open Access
- 1 October 2021
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 22 (19) , 10673
Evolution of Electronic State and Properties of Silver Nanoparticles during Their Formation in Aqueous Solution
The electron density of a nanoparticle is a very important characteristic of the properties of a material. This paper describes the formation of silver nanoparticles (NPs) and the variation in the electronic state of an NP’s surface upon the reduction in Ag+ ions with oxalate ions, induced by UV irradiation. The calculations were based on optical spectrophotometry data. The NPs were characterized using Transmission electron microscopy and Dynamic light scattering. As ~10 nm nanoparticles are formed, the localized surface plasmon resonance (LSPR) band increases in intensity, decreases in width, and shifts to the UV region from 402 to 383 nm. The interband transitions (IBT) band (≤250 nm) increases in intensity, with the band shape and position remaining unchanged. The change in the shape and position of the LSPR band of silver nanoparticles in the course of their formation is attributable to an increasing concentration of free electrons in the particles as a result of a reduction in Ag+ ions on the surface and electron injection by radicals. The ζ-potential of colloids increases with an increase in electron density in silver nuclei. A quantitative relationship between this shift and electron density on the surface was derived on the basis of the Mie–Drude theory. The observed blue shift (19 nm) corresponds to an approximately 10% increase in the concentration of electrons in silver nanoparticles.- 1 October 2021
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 22 (19) , 10673
Open AccessEvolution of Electronic State and Properties of Silver Nanoparticles during Their Formation in Aqueous Solution
The electron density of a nanoparticle is a very important characteristic of the properties of a material. This paper describes the formation of silver nanoparticles (NPs) and the variation in the electronic state of an NP’s surface upon the reduction in Ag+ ions with oxalate ions, induced by UV irradiation. The calculations were based on optical spectrophotometry data. The NPs were characterized using Transmission electron microscopy and Dynamic light scattering. As ~10 nm nanoparticles are formed, the localized surface plasmon resonance (LSPR) band increases in intensity, decreases in width, and shifts to the UV region from 402 to 383 nm. The interband transitions (IBT) band (≤250 nm) increases in intensity, with the band shape and position remaining unchanged. The change in the shape and position of the LSPR band of silver nanoparticles in the course of their formation is attributable to an increasing concentration of free electrons in the particles as a result of a reduction in Ag+ ions on the surface and electron injection by radicals. The ζ-potential of colloids increases with an increase in electron density in silver nuclei. A quantitative relationship between this shift and electron density on the surface was derived on the basis of the Mie–Drude theory. The observed blue shift (19 nm) corresponds to an approximately 10% increase in the concentration of electrons in silver nanoparticles. - Open Access
The New Approach to the Preparation of Polyacrylamide-Based Hydrogels: Initiation of Polymerization of Acrylamide with 1,3-Dimethylimidazolium (Phosphonooxy-)Oligosulphanide under Drying Aqueous Solutions
The new initiator of the polymerization of acrylamide, leading to the formation of crosslinked polyacrylamide, was discovered. The structure of the synthesized polyacrylamide was characterized by XRD, 1H NMR, and 13C NMR spectroscopy. It was shown that 1,3-dimethylimidazolium (phosphonooxy-)oligosulphanide is able to initiate radical polymerization under drying aqueous solutions of acrylamide, even at room temperature. According to XRF data, the synthesized polyacrylamide gel contains 0.28 wt% of sulphur. The formed polymer network has a low crosslinking density and a high equilibrium degree of swelling. The swelling rate of polyacrylamide gel in water corresponds to the first order kinetic equation with the rate constant 6.2 × 10−2 min−1. The initiator is promising for combining acrylamide polymerization with the processes of gel molding and drying.
Open AccessThe New Approach to the Preparation of Polyacrylamide-Based Hydrogels: Initiation of Polymerization of Acrylamide with 1,3-Dimethylimidazolium (Phosphonooxy-)Oligosulphanide under Drying Aqueous Solutions
The new initiator of the polymerization of acrylamide, leading to the formation of crosslinked polyacrylamide, was discovered. The structure of the synthesized polyacrylamide was characterized by XRD, 1H NMR, and 13C NMR spectroscopy. It was shown that 1,3-dimethylimidazolium (phosphonooxy-)oligosulphanide is able to initiate radical polymerization under drying aqueous solutions of acrylamide, even at room temperature. According to XRF data, the synthesized polyacrylamide gel contains 0.28 wt% of sulphur. The formed polymer network has a low crosslinking density and a high equilibrium degree of swelling. The swelling rate of polyacrylamide gel in water corresponds to the first order kinetic equation with the rate constant 6.2 × 10−2 min−1. The initiator is promising for combining acrylamide polymerization with the processes of gel molding and drying.
- Open Access
- 3 April 2021
- Published by Taylor & Francis in Green Chemistry Letters and Reviews
- Vol. 14 (2) , 435-441
The product of interaction of elemental sulfur and dimethylphosphate 1,3-dimethylimidazolium is a new green initiator of formaldehyde polymerization
Interaction of 1,3-dimethylimidazolium dimethylphosphate and elemental sulfur synthesized a new initiator of polymerization of formaldehyde, opening the possibility of its implementation in accordance with the principles of Green chemistry. The possibility of fast oligomerization of formaldehyde in an aqueous medium with the formation of insoluble products, the structure of which is determined by FTIR, MALDI-TOF, 1H NMR, 13C NMR, HSQC and HMBC spectroscopy, is shown. It was found that (phosphonooxy-)oligosulfanide anion initiates formaldehyde oligomerization by anionic mechanism with chain termination due to interaction with water. It was shown that the synthesized formaldehyde oligomers retain resistance to degradation up to a temperature of 443 K, and then slowly thermally decompose to a temperature of 513 K, above which the rate of thermal degradation increases significantly. GRAPHICAL ABSTRACT
- 3 April 2021
- Published by Taylor & Francis in Green Chemistry Letters and Reviews
- Vol. 14 (2) , 435-441
Open AccessThe product of interaction of elemental sulfur and dimethylphosphate 1,3-dimethylimidazolium is a new green initiator of formaldehyde polymerization
Interaction of 1,3-dimethylimidazolium dimethylphosphate and elemental sulfur synthesized a new initiator of polymerization of formaldehyde, opening the possibility of its implementation in accordance with the principles of Green chemistry. The possibility of fast oligomerization of formaldehyde in an aqueous medium with the formation of insoluble products, the structure of which is determined by FTIR, MALDI-TOF, 1H NMR, 13C NMR, HSQC and HMBC spectroscopy, is shown. It was found that (phosphonooxy-)oligosulfanide anion initiates formaldehyde oligomerization by anionic mechanism with chain termination due to interaction with water. It was shown that the synthesized formaldehyde oligomers retain resistance to degradation up to a temperature of 443 K, and then slowly thermally decompose to a temperature of 513 K, above which the rate of thermal degradation increases significantly. GRAPHICAL ABSTRACT
- Open Access
- 1 March 2021
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 11 (15) , 9008-9020
Elemental sulphur in the synthesis of sulphur-containing polymers: reaction mechanisms and green prospects
The synthesis of polymers using elemental sulphur as a chemical agent has been studied in relation to the worldwide overproduction of cyclo-octasulphur. Herein, the mechanisms of the processes leading to the inclusion of elemental sulphur into macromolecules have been reviewed and the main methods for reduction of the reaction temperature required for the S8 ring opening have been shown. Approaches to the activation of cyclo-octasulphur in the synthesis and macromolecule cross-linking reactions were discussed in the context of finding the chemical agents and conditions that satisfy the principles of green chemistry.
- 1 March 2021
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 11 (15) , 9008-9020
Open AccessElemental sulphur in the synthesis of sulphur-containing polymers: reaction mechanisms and green prospects
The synthesis of polymers using elemental sulphur as a chemical agent has been studied in relation to the worldwide overproduction of cyclo-octasulphur. Herein, the mechanisms of the processes leading to the inclusion of elemental sulphur into macromolecules have been reviewed and the main methods for reduction of the reaction temperature required for the S8 ring opening have been shown. Approaches to the activation of cyclo-octasulphur in the synthesis and macromolecule cross-linking reactions were discussed in the context of finding the chemical agents and conditions that satisfy the principles of green chemistry.