Г. С. Бородкин

1.5k total citations
181 papers, 1.2k citations indexed

About

Г. С. Бородкин is a scholar working on Organic Chemistry, Materials Chemistry and Oncology. According to data from OpenAlex, Г. С. Бородкин has authored 181 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 124 papers in Organic Chemistry, 59 papers in Materials Chemistry and 39 papers in Oncology. Recurrent topics in Г. С. Бородкин's work include Metal complexes synthesis and properties (39 papers), Photochromic and Fluorescence Chemistry (30 papers) and Synthesis and Characterization of Heterocyclic Compounds (25 papers). Г. С. Бородкин is often cited by papers focused on Metal complexes synthesis and properties (39 papers), Photochromic and Fluorescence Chemistry (30 papers) and Synthesis and Characterization of Heterocyclic Compounds (25 papers). Г. С. Бородкин collaborates with scholars based in Russia, Belarus and Egypt. Г. С. Бородкин's co-authors include Владимир И. Минкин, А. Д. Гарновский, А. С. Бурлов, В. Г. Власенко, А. В. Метелица, А. И. Ураев, Igor S. Vasilchenko, А. Г. Стариков, Л. Н. Диваева and Yu. V. Koshchienko and has published in prestigious journals such as SHILAP Revista de lepidopterología, Inorganic Chemistry and The Journal of Organic Chemistry.

In The Last Decade

Г. С. Бородкин

167 papers receiving 1.2k citations

Peers

Г. С. Бородкин
Г. С. Бородкин
Citations per year, relative to Г. С. Бородкин Г. С. Бородкин (= 1×) peers Л. Д. Попов

Countries citing papers authored by Г. С. Бородкин

Since Specialization
Citations

This map shows the geographic impact of Г. С. Бородкин'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 Г. С. Бородкин with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Г. С. Бородкин more than expected).

Fields of papers citing papers by Г. С. Бородкин

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Г. С. Бородкин. 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 Г. С. Бородкин. The network helps show where Г. С. Бородкин may publish in the future.

Co-authorship network of co-authors of Г. С. Бородкин

This figure shows the co-authorship network connecting the top 25 collaborators of Г. С. Бородкин. A scholar is included among the top collaborators of Г. С. Бородкин 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 Г. С. Бородкин. Г. С. Бородкин is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Пугачев, Артем Д., И. Н. Бардасов, Г. С. Бородкин, et al.. (2025). New Benzimidazole-Based pH-Sensitive Fluorescent Probes. Molecules. 30(23). 4622–4622.
2.
Butova, Vera V., Ilya V. Ozhogin, Артем Д. Пугачев, et al.. (2024). Introduction of photochromic properties to UiO-66-NH2 via “click”-modification by spiropyran molecule. Microporous and Mesoporous Materials. 374. 113151–113151. 2 indexed citations
3.
Пугачев, Артем Д., Ilya V. Ozhogin, Ирина А. Ростовцева, et al.. (2024). Structure–Properties Correlations in the Range of Cationic Spiropyrans as Analogues of Cyanine Dyes. ChemistrySelect. 9(10). 1 indexed citations
4.
Makarova, Nadezhda I., et al.. (2024). Facile approach to N,O,S-heteropentacycles via condensation of sterically crowded 3 H -phenoxazin-3-one with ortho- substituted anilines. Beilstein Journal of Organic Chemistry. 20. 336–345.
5.
Ozhogin, Ilya V., Peter V. Zolotukhin, Nadezhda I. Makarova, et al.. (2024). Meta-stable state photoacid containing β-estradiol fragment with photomodulated biological activity and anti-cancer stem cells properties. Journal of Photochemistry and Photobiology B Biology. 257. 112964–112964. 4 indexed citations
6.
Ozhogin, Ilya V., Артем Д. Пугачев, Ирина А. Ростовцева, et al.. (2024). Synthesis, experimental and theoretical studies of nitrosubstituted symmetric bis(spiropyran) of the indoline series. Russian Chemical Bulletin. 73(9). 2708–2724.
7.
Ukhin, L. Yu., et al.. (2023). New reactions of 2,3-diaminonaphthaline with carbonyl electrophiles. Mendeleev Communications. 33(1). 115–117.
8.
Пугачев, Артем Д., Nadezhda I. Makarova, Ирина А. Ростовцева, et al.. (2023). Molecular design and synthesis of methoxy-substitued spiropyrans with photomodulated NIR-fluorescence. Photochemical & Photobiological Sciences. 22(11). 2651–2673. 5 indexed citations
9.
Ozhogin, Ilya V., Артем Д. Пугачев, Ирина А. Ростовцева, et al.. (2023). New cationic spiropyrans with photoswitchable NIR fluorescence. Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy. 297. 122712–122712. 9 indexed citations
10.
11.
Пугачев, Артем Д., Ilya V. Ozhogin, Valery V. Tkachev, et al.. (2023). Comprehensive study of substituent effects on structure and photochromic properties of 1,3-benzoxazine-4-one spiropyrans. Journal of Molecular Structure. 1277. 134898–134898. 8 indexed citations
12.
Пугачев, Артем Д., Ilya V. Ozhogin, Г. С. Бородкин, et al.. (2023). Condensation of formyl-substituted indoline spiropyrans with 3H-indolium salts: specific features. Russian Chemical Bulletin. 72(4). 979–989. 2 indexed citations
13.
Koshchienko, Yu. V., et al.. (2023). Bromination of 1(9)H-2,3-Dihydroimidazo[1,2-a]benzimidazole and Its N-Derivatives. Russian Journal of General Chemistry. 93(6). 1344–1351. 1 indexed citations
14.
Ozhogin, Ilya V., Артем Д. Пугачев, Ирина А. Ростовцева, et al.. (2023). Methyl 5′-Chloro-8-formyl-5-hydroxy-1′,3′,3′-trimethyl-spiro-[chromene-2,2′-indoline]-6-carboxylate. SHILAP Revista de lepidopterología. 2023(1). M1549–M1549. 1 indexed citations
15.
Ozhogin, Ilya V., Артем Д. Пугачев, Nadezhda I. Makarova, et al.. (2023). Novel Indoline Spiropyrans Based on Human Hormones β-Estradiol and Estrone: Synthesis, Structure, Chromogenic and Cytotoxic Properties. Molecules. 28(9). 3866–3866. 4 indexed citations
16.
Пугачев, Артем Д., Ilya V. Ozhogin, Nadezhda I. Makarova, et al.. (2021). Novel polychromogenic fluorine-substituted spiropyrans demonstrating either uni- or bidirectional photochromism as multipurpose molecular switches. Dyes and Pigments. 199. 110043–110043. 25 indexed citations
17.
Babkov, Denis A., E. V. Sokolova, Alexandra A. Kolodina, et al.. (2019). Towards multi-target antidiabetic agents: Discovery of biphenyl-benzimidazole conjugates as AMPK activators. Bioorganic & Medicinal Chemistry Letters. 29(17). 2443–2447. 37 indexed citations
18.
Зарубаев, Владимир В., et al.. (2016). Tautomeric and non-tautomeric N-substituted 2-iminobenzimidazolines as new lead compounds for the design of anti-influenza drugs: An in vitro study. Bioorganic & Medicinal Chemistry. 24(22). 5796–5803. 6 indexed citations
19.
Бурлов, А. С., et al.. (2016). Synthesis and structure of enaminoketones of pyrazole containing 2-thione(selenone)benzimidazolyl fragments and their zinc and cadmium complexes. Russian Journal of General Chemistry. 86(4). 876–884. 2 indexed citations
20.
Бородкин, Г. С., et al.. (2011). Heteronuclear NMR spectroscopy in the coordination chemistry. Russian Journal of Coordination Chemistry. 37(8). 565–571. 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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