А. В. Афонин
About
А. В. Афонин is a scholar working on Organic Chemistry, Physical and Theoretical Chemistry and Spectroscopy.
According to data from OpenAlex, А. В. Афонин has authored 231 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 182 papers in Organic Chemistry, 43 papers in Physical and Theoretical Chemistry and 43 papers in Spectroscopy. Recurrent topics in А. В. Афонин's work include Synthesis and Reactions of Organic Compounds (40 papers), Fluorine in Organic Chemistry (34 papers) and Synthesis and Characterization of Pyrroles (34 papers). А. В. Афонин is often cited by papers focused on Synthesis and Reactions of Organic Compounds (40 papers), Fluorine in Organic Chemistry (34 papers) and Synthesis and Characterization of Pyrroles (34 papers). А. В. Афонин collaborates with scholars based in Russia, Poland and Argentina. А. В. Афонин's co-authors include Alexander V. Vashchenko, Б. А. Трофимов, Igor А. Ushakov, Lina P. Nikitina, Kseniya V. Belyaeva, M. V. SIGALOV, Anastasiya G. Mal’kina, Ludmila V. Andriyankova, А. Й. Михалева and Elena Yu. Schmidt and has published in prestigious journals such as SHILAP Revista de lepidopterología, Chemical Communications and Physical Chemistry Chemical Physics.
In The Last Decade
А. В. Афонин
216 papers receiving 1.7k citations
Peers
А. В. Афонин
Régis Goumont France
Alexander V. Vashchenko Russia
А. Ф. Пожарский Russia
Benzion Fuchs Israel
Dmitrii S. Yufit United Kingdom
Sebastian M. Walter Germany
Kenneth B. Ling United Kingdom
N. N. Chípanina Russia
T. Połoński Poland
Michael G. Chudzinski Canada
Citations per year, relative to А. В. Афонин А. В. Афонин (= 1×)
peers
Régis Goumont
Countries citing papers authored by А. В. Афонин
Since
Specialization
Citations
This map shows the geographic impact of А. В. Афонин'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 А. В. Афонин with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites А. В. Афонин more than expected).
Fields of papers citing papers by А. В. Афонин
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by А. В. Афонин. 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 А. В. Афонин. The network helps show where А. В. Афонин may publish in the future.
Co-authorship network of co-authors of А. В. Афонин
This figure shows the co-authorship network connecting the top 25 collaborators of А. В. Афонин. A scholar is included among the top collaborators of А. В. Афонин 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 А. В. Афонин. А. В. Афонин is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Афонин, А. В., Danuta Rusińska‐Roszak, & Dmitry I. Pavlov. (2025). Fine tuning the optical properties and Frontier orbital energy in pyrrolylenones as an example of D–π–A sensitizers via functionalization of the molecular backbone. New Journal of Chemistry. 49(9). 3672–3687.
2.
Belyaeva, Kseniya V., et al.. (2024). Annulation of 1-methylisoquinoline with pyrrolylacetylenic ketones: catalyst-free stereoselective synthesis of (E)-acylethenylpyrrolo[1’,2’:3,4]imidazo[2,1-a]isoquinolines. Mendeleev Communications. 34(5). 691–693.
3.
Афонин, А. В. & Danuta Rusińska‐Roszak. (2024). Evidence for the O−H⋅⋅⋅O=C Resonance‐Assisted Hydrogen Bond in Tropolones and Quantification of its σ‐ and π‐Components Using Molecular Tailoring Approach. ChemPhysChem. 25(23). e202400698–e202400698.
4.
Афонин, А. В. & Danuta Rusińska‐Roszak. (2023). Revealing the Reasons for Degeneration of Resonance-Assisted Hydrogen Bond on the Aromatic Platform: Calculations of Ortho-, Meta-, Para-Disubstituted Benzenes, and (Z)-(E)-Olefins. Molecules. 28(2). 536–536.
5.
Nikitina, Lina P., Kseniya V. Belyaeva, А. В. Афонин, Igor А. Ushakov, & Б. А. Трофимов. (2023). One-pot synthesis of <i>N</i>-acylethenyl4-acylethenyliminodihydroquinolines from 4-aminoquinoline and alkynones. Журнал органической химии. 59(3). 316–322.
6.
Афонин, А. В. & Danuta Rusińska‐Roszak. (2023). Quantification of hydrogen bond energy based on equations using spectroscopic, structural, QTAIM-based, and NBO-based descriptors which calibrated by the molecular tailoring approach. Journal of Molecular Modeling. 30(1).
7.
Belyaeva, Kseniya V., et al.. (2022). A straightforward access to 2-hydroxyoxazino[3,2-f ]phenanthridines from phenanthridine, oxalylacetylenes and water. Mendeleev Communications. 32(4). 439–442.
8.
Афонин, А. В., Irina V. Sterkhova, Alexander V. Vashchenko, & M. V. SIGALOV. (2018). Estimating the energy of intramolecular bifurcated (three-centered) hydrogen bond by X-ray, IR and 1 H NMR spectroscopy, and QTAIM calculations. Journal of Molecular Structure. 1163. 185–196.
9.
Афонин, А. В., et al.. (2018). Case study of 2-vinyloxypyridine: Quantitative assessment of the intramolecular C H⋯N hydrogen bond energy and its contribution to the one-bond 13C1H coupling constant. Journal of Molecular Structure. 1176. 73–85.
10.
Короткова, О. Г., et al.. (2016). The Influence of Crushing of Wheat Bran on the Properties and Reactivity to Biocatalytic Conversion. Kataliz v promyshlennosti. 16(5). 75–82.
11.
Belyaeva, Kseniya V., Lina P. Nikitina, Irina Yu. Bagryanskaya, et al.. (2015). Reaction of 1-substituted benzimidazoles with acylacetylenes and water: ring-opening versus ring-expansion and isotopic effect of deuterium. Tetrahedron. 71(19). 2891–2899.
12.
Афонин, А. В., Igor А. Ushakov, Alexander V. Vashchenko, Evgeniy V. Kondrashov, & Alexander Yu. Rulev. (2010). GIAO, DFT, AIM and NBO analysis of the NH···O intramolecular hydrogen‐bond influence on the 1J(N,H) coupling constant in push–pull diaminoenones. Magnetic Resonance in Chemistry. 48(9). 661–670.
13.
Афонин, А. В., et al.. (2010). Study of conformations and hydrogen bonds in the configurational isomers of pyrrole‐2‐carbaldehyde oxime by 1H, 13C and 15N NMR spectroscopy combined with MP2 and DFT calculations and NBO analysis. Magnetic Resonance in Chemistry. 48(9). 685–692.
14.
Афонин, А. В. & Alexander V. Vashchenko. (2010). Theoretical study of bifurcated hydrogen bonding effects on the 1J(N,H), 1hJ(N,H), 2hJ(N,N) couplings and 1H, 15N shieldings in model pyrroles. Magnetic Resonance in Chemistry. 48(4). 309–317.
15.
Афонин, А. В., et al.. (2009). Comparative analysis of 13C shielding constants stereospecificity in the silicon and germanium derivatives of acetylenic aldehyde and ketone oximes based on the 13C NMR spectroscopy and GIAO calculations. Magnetic Resonance in Chemistry. 47(7). 601–604.
16.
Афонин, А. В., et al.. (2008). Comparative analysis of hydrogen bonding with participation of the nitrogen, oxygen and sulfur atoms in the 2(2′‐heteroaryl)pyrroles and their trifluoroacetyl derivatives based on the 1H, 13C, 15N spectroscopy and DFT calculations. Magnetic Resonance in Chemistry. 46(5). 441–447.
17.
Афонин, А. В., Igor А. Ushakov, Alexander V. Vashchenko, et al.. (2008). CH···N and CH···O intramolecular hydrogen bonding effects in the 1H, 13C and 15 N NMR spectra of the configurational isomers of 1‐vinylpyrrole‐2‐carbaldehyde oxime substantiated by DFT calculations. Magnetic Resonance in Chemistry. 47(2). 105–112.
18.
Афонин, А. В., Igor А. Ushakov, А. Й. Михалева, & Б. А. Трофимов. (2007). Bifurcated hydrogen‐bonding effect on the shielding and coupling constants in trifluoroacetyl pyrroles as studied by 1H, 13C and 15N NMR spectroscopy and DFT calculations. Magnetic Resonance in Chemistry. 45(3). 220–230.
19.
Афонин, А. В., Igor А. Ushakov, Lyubov N. Sobenina, et al.. (2005). Different types of hydrogen bonds in 2‐substituted pyrroles and 1‐vinyl pyrroles as monitored by 1H, 13C and 15N NMR spectroscopy and ab initio calculations. Magnetic Resonance in Chemistry. 44(1). 59–65.
20.
Афонин, А. В., et al.. (1989). Reaction of 1-vinylpyrazoles with tetracyanoethylene. Chemistry of Heterocyclic Compounds. 25(7). 768–771.
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