L. М. Timofeeva

838 total citations · 1 hit paper
21 papers, 686 citations indexed

About

L. М. Timofeeva is a scholar working on Organic Chemistry, Spectroscopy and Physical and Theoretical Chemistry. According to data from OpenAlex, L. М. Timofeeva has authored 21 papers receiving a total of 686 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Organic Chemistry, 6 papers in Spectroscopy and 4 papers in Physical and Theoretical Chemistry. Recurrent topics in L. М. Timofeeva's work include Antimicrobial agents and applications (9 papers), Advanced Polymer Synthesis and Characterization (6 papers) and Molecular Spectroscopy and Structure (4 papers). L. М. Timofeeva is often cited by papers focused on Antimicrobial agents and applications (9 papers), Advanced Polymer Synthesis and Characterization (6 papers) and Molecular Spectroscopy and Structure (4 papers). L. М. Timofeeva collaborates with scholars based in Russia. L. М. Timofeeva's co-authors include N. A. Kleshcheva, М. П. Филатова, A. K. Lyashchenko, Margarita O. Shleeva, Arseny S. Kaprelyants, G.E. Chudinov, M. V. Basilevsky, N. P. Yevlampieva, Г. И. Тимофеева and Г. Н. Бондаренко and has published in prestigious journals such as Applied Microbiology and Biotechnology, Biomacromolecules and Journal of Molecular Liquids.

In The Last Decade

L. М. Timofeeva

19 papers receiving 676 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Antimicrobial polymers: mechanism of action, factors of activity, and applications

2010 485 citations L. М. Timofeeva, N. A. Kleshcheva Applied Microbiology and Biotechnology profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
L. М. Timofeeva Russia	8	545	183	173	91	84	21	686
N. A. Kleshcheva Russia	8	521 1.0×	178 1.0×	167 1.0×	90 1.0×	82 1.0×	17	651
O. Bouloussa France	9	350 0.6×	245 1.3×	94 0.5×	75 0.8×	139 1.7×	13	797
M. Firat Ilker United States	5	539 1.0×	249 1.4×	281 1.6×	90 1.0×	39 0.5×	5	704
Matthias Haeussler Australia	9	335 0.6×	138 0.8×	188 1.1×	76 0.8×	63 0.8×	15	513
Pinar Kurt United States	10	265 0.5×	58 0.3×	49 0.3×	73 0.8×	82 1.0×	11	454
Rocío Cuervo‐Rodríguez Spain	17	360 0.7×	98 0.5×	42 0.2×	231 2.5×	83 1.0×	39	621
Kristen P. Miller United States	7	243 0.4×	225 1.2×	99 0.6×	66 0.7×	261 3.1×	11	681
Qiao Yuan China	12	281 0.5×	85 0.5×	123 0.7×	76 0.8×	62 0.7×	45	573

Countries citing papers authored by L. М. Timofeeva

Since Specialization

Citations

This map shows the geographic impact of L. М. Timofeeva's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by L. М. Timofeeva with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites L. М. Timofeeva more than expected).

Fields of papers citing papers by L. М. Timofeeva

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by L. М. Timofeeva. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by L. М. Timofeeva. The network helps show where L. М. Timofeeva may publish in the future.

Co-authorship network of co-authors of L. М. Timofeeva

This figure shows the co-authorship network connecting the top 25 collaborators of L. М. Timofeeva. A scholar is included among the top collaborators of L. М. Timofeeva based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with L. М. Timofeeva. L. М. Timofeeva is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Еременко, И.Л., et al.. (2025). Antimicrobial protonated polydiallylamines: how to retain bactericidal efficiency at minimal toxicity. Mendeleev Communications. 35(4). 450–453.

Еременко, И.Л., М. П. Филатова, N. P. Yevlampieva, et al.. (2024). Optimization of Methodology of Protonated Diallylammonium Monomers Free Radical Polymerization for the Obtaining Polymers with a Low Molecular Weight. Russian Journal of Applied Chemistry. 97(6). 550–560. 1 indexed citations

Timofeeva, L. М., Г. Н. Бондаренко, Vadim Nikitushkin, et al.. (2022). On the molecular mechanism of nonspecific antimicrobial action of protonated diallylammonium polymers on mycobacterial cells. European Polymer Journal. 171. 111214–111214. 5 indexed citations

Topchiy, Maxim A., М. П. Филатова, N. P. Yevlampieva, et al.. (2019). Impact of the RAFT/MADIX agent on protonated diallylammonium monomer cyclopolymerization with efficient chain transfer to monomer. European Polymer Journal. 122. 109363–109363. 7 indexed citations

Yevlampieva, N. P., et al.. (2018). Protonated member of poly(diallylammonium) family: Hydrodynamic and conformational properties. International Journal of Polymer Analysis and Characterization. 23(5). 403–414. 5 indexed citations

Филатова, М. П., et al.. (2018). Radical Polymerization of Protonated Diallylammonium Monomers in Bidistilled Aqueous Solution: Kinetic Study. Polymer Science Series B. 60(4). 445–454. 5 indexed citations

Lyashchenko, A. K., et al.. (2017). Hydration and dielectrical properties of aqueous pyrrolidinium trifluoroacetate solutions. Russian Journal of Physical Chemistry A. 91(10). 1913–1918.

Timofeeva, L. М., et al.. (2017). General trends in concentration and temperature behavior of equivalent conductance of N,N-diallylammonium polymers aqueous solutions: Effect of counterion nature and amine structure. Polymer Science Series C. 59(1). 141–148. 2 indexed citations

Timofeeva, L. М., et al.. (2015). Nonquaternary poly(diallylammonium) polymers with different amine structure and their biocidal effect on Mycobacterium tuberculosis and Mycobacterium smegmatis. Applied Microbiology and Biotechnology. 99(6). 2557–2571. 22 indexed citations

10.

Lyashchenko, A. K., et al.. (2014). Microwave dielectric properties of aqueous trifluoroacetic acid solutions. Russian Journal of Inorganic Chemistry. 59(12). 1530–1537. 1 indexed citations

11.

Lyashchenko, A. K., et al.. (2013). Microwave dielectric permittivity and relaxation for aqueous potassium trifluoroacetate solutions. Russian Journal of Inorganic Chemistry. 58(7). 880–885. 4 indexed citations

12.

Timofeeva, L. М. & N. A. Kleshcheva. (2010). Antimicrobial polymers: mechanism of action, factors of activity, and applications. Applied Microbiology and Biotechnology. 89(3). 475–492. 485 indexed citations breakdown →

13.

Timofeeva, L. М., et al.. (2009). Secondary and Tertiary Polydiallylammonium Salts: Novel Polymers with High Antimicrobial Activity. Biomacromolecules. 10(11). 2976–2986. 71 indexed citations

14.

Timofeeva, L. М., et al.. (2008). Effect of dielectric properties and structure of aqueous solutions of diallylammonium salts on their reactivity in radical polymerization. Polymer Science Series A. 50(3). 273–282. 7 indexed citations

15.

Lyashchenko, A. K., et al.. (2006). The hydrophobic hydration in aqueous solutions of allyl-substituted ammonium salts. Journal of Molecular Liquids. 131-132. 101–104. 9 indexed citations

16.

Timofeeva, L. М., et al.. (2006). Effect of dielectric and structural properties of solutions on the polymerizability of diallylammonium-type monomers. Doklady Physical Chemistry. 406(2). 53–56. 3 indexed citations

17.

Timofeeva, L. М., et al.. (2002). Radical polymerization of diallylamine compounds: From quantum chemical modeling to controllable synthesis of high‐molecular‐weight polymers. International Journal of Quantum Chemistry. 88(5). 531–541. 16 indexed citations

18.

Timofeeva, L. М., et al.. (2002). Synthesis of High‐Molecular Weight Polymers Based on N,N‐Diallyl‐N‐Methylamine. Macromolecular Chemistry and Physics. 203(16). 2296–2304. 14 indexed citations

19.

Kleshcheva, N. A., et al.. (2000). Synthesis of high-molecular-weight polyamine by radical polymerization ofN,N-diallyl-N-methylamine. Russian Chemical Bulletin. 49(3). 431–437. 5 indexed citations

20.

Basilevsky, M. V., et al.. (1993). Application of the configuration interaction method for quantum-chemical calculations of solvation effects. Chemical Physics. 173(3). 345–355. 12 indexed citations

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