Н. Г. Бичан
About
Н. Г. Бичан is a scholar working on Materials Chemistry, Organic Chemistry and Electrical and Electronic Engineering.
According to data from OpenAlex, Н. Г. Бичан has authored 70 papers receiving a total of 564 indexed citations (citations by other indexed papers that have themselves been cited), including 66 papers in Materials Chemistry, 40 papers in Organic Chemistry and 18 papers in Electrical and Electronic Engineering. Recurrent topics in Н. Г. Бичан's work include Porphyrin and Phthalocyanine Chemistry (59 papers), Fullerene Chemistry and Applications (33 papers) and Molecular Junctions and Nanostructures (15 papers). Н. Г. Бичан is often cited by papers focused on Porphyrin and Phthalocyanine Chemistry (59 papers), Fullerene Chemistry and Applications (33 papers) and Molecular Junctions and Nanostructures (15 papers). Н. Г. Бичан collaborates with scholars based in Russia, France and Italy. Н. Г. Бичан's co-authors include Т. Н. Ломова, Е. Н. Овченкова, N.O. Kudryakova, Alexander A. Ksenofontov, М. С. Груздев, I. V. Shelaev, А. С. Семейкин, Arshak A. Tsaturyan, F. E. Gostev and Ilya A. Khodov and has published in prestigious journals such as The Journal of Physical Chemistry C, Inorganic Chemistry and Tetrahedron.
In The Last Decade
Н. Г. Бичан
67 papers receiving 559 citations
Peers
Н. Г. Бичан
Е. Н. Овченкова Russia
Catherine Bronner Germany
Stephen M. Woessner United States
De‐Hong Wu China
Yi‐Hwa Song Taiwan
Issiah B. Lozada Canada
Takafumi Osuga Japan
Jorge H. S. K. Monteiro United States
Benjamin Hupp Germany
I.H.T. Sham Hong Kong
Citations per year, relative to Н. Г. Бичан Н. Г. Бичан (= 1×)
peers
Е. Н. Овченкова
Countries citing papers authored by Н. Г. Бичан
Since
Specialization
Citations
This map shows the geographic impact of Н. Г. Бичан'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 Н. Г. Бичан with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Н. Г. Бичан more than expected).
Fields of papers citing papers by Н. Г. Бичан
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by Н. Г. Бичан. 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 Н. Г. Бичан. The network helps show where Н. Г. Бичан may publish in the future.
Co-authorship network of co-authors of Н. Г. Бичан
This figure shows the co-authorship network connecting the top 25 collaborators of Н. Г. Бичан. A scholar is included among the top collaborators of Н. Г. Бичан 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 Н. Г. Бичан. Н. Г. Бичан is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Бичан, Н. Г., Е. Н. Овченкова, Arshak A. Tsaturyan, et al.. (2025). Coordination Self-Assembly and Photophysical Properties of Dyads Based on Carbazole-Substituted Cobalt(II) Phthalocyanine and Pyridyl-Functionalized Fullerene and Anthracene. Inorganic Chemistry. 64(28). 14249–14260.
2.
Овченкова, Е. Н., et al.. (2025). Soluble peripherally tert-butylphenoxy/tert-butylcarbazole substituted zinc phthalocyanines and their photophysical properties. Polyhedron. 270. 117447–117447.
3.
Chervonova, U. V., Н. Г. Бичан, Alexander A. Ksenofontov, & М. С. Груздев. (2024). Heterofunctional β-diketones incorporating ester linkages: Mesomorphism and solvatochromic effect. Journal of Molecular Liquids. 417. 126572–126572.
4.
Груздев, М. С., et al.. (2024). New Branched Iron(III) Complexes in Fluorescent Environment Created by Carbazole Moieties: Synthesis and Structure, Static Magnetic and Resonance Properties. Magnetochemistry. 10(6). 38–38.
5.
Груздев, М. С., et al.. (2024). Azomethine Fe3+ coordination compounds containing carbazole units: Synthetic approach, spectral characterization, and magnetic studies. Applied Organometallic Chemistry. 38(5).
6.
Овченкова, Е. Н., Arshak A. Tsaturyan, Н. Г. Бичан, et al.. (2024). Axial Coordinated Manganese(III) Porphyrin/Tetraazaporphyrin – 4‐(10‐phenylanthracen‐9‐yl)Pyridine Dyads: Self‐Assembly, Structure and Spectral Properties in Ground and Excited States. Chemistry - An Asian Journal. 19(13). e202400095–e202400095.
7.
Chervonova, U. V., et al.. (2023). Chemical functionalization and optical properties of new fluorescent building blocks bearing carbazole moieties. Optical Materials. 147. 114754–114754.
8.
Овченкова, Е. Н., Н. Г. Бичан, Alexander A. Ksenofontov, I. V. Shelaev, & Т. Н. Ломова. (2023). Spectroscopic and computational characterization of new promising donors – Manganese(III) porphyrins bearing carbazole groups. Polyhedron. 250. 116813–116813.
9.
Бичан, Н. Г., et al.. (2023). Spectral Studies of Coordination of 1-Methyl-2-(pyridin-4-yl)-3,4-fullero[60]pyrrolidine by Highly Substituted Cobalt(II) Porphyrin. Russian Journal of Inorganic Chemistry. 68(7). 853–860.
10.
Овченкова, Е. Н., Н. Г. Бичан, & Т. Н. Ломова. (2023). Synthesis, Chemical Structure, and Ground- and Excited-State Spectral Characteristics of (Porphyrinato)(chloro)indium(III) and Its Complexes with C60 and Pyridyl-Substituted Fullero[60]pyrrolidine. Russian Journal of Inorganic Chemistry. 68(11). 1562–1570.
11.
Бичан, Н. Г., Е. Н. Овченкова, Alexander A. Ksenofontov, et al.. (2022). Meso-carbazole substituted porphyrin complexes: Synthesis and spectral properties according to experiment, DFT calculations and the prediction by machine learning methods. Dyes and Pigments. 204. 110470–110470.
12.
Бичан, Н. Г., Е. Н. Овченкова, Alexander A. Ksenofontov, et al.. (2022). Donor–Acceptor Complexes of (5,10,15,20-Tetra(4-methylphenyl)porphyrinato)cobalt(II) with Fullerenes C60: Self-Assembly, Spectral, Electrochemical and Photophysical Properties. Molecules. 27(24). 8900–8900.
13.
Бичан, Н. Г., Arshak A. Tsaturyan, Е. Н. Овченкова, et al.. (2022). Donor–acceptor interactions of gold(iii ) porphyrins with cobalt(ii ) phthalocyanine: chemical structure of products, their spectral characterization and DFT study. Dalton Transactions. 51(23). 9072–9084.
14.
Овченкова, Е. Н., Н. Г. Бичан, М. С. Груздев, et al.. (2021). Carbazole-functionalized cobalt(ii ) porphyrin axially bonded with C60/C70 derivatives: synthesis and characterization. New Journal of Chemistry. 45(20). 9053–9065.
15.
Овченкова, Е. Н., Arshak A. Tsaturyan, Н. Г. Бичан, & Т. Н. Ломова. (2021). N Basicity of Substituted Fullero[60]/[70]pyrrolidines According to DFT/TD-DFT Calculations and Chemical Thermodynamics. The Journal of Physical Chemistry A. 125(24). 5365–5374.
16.
Овченкова, Е. Н., Н. Г. Бичан, Arshak A. Tsaturyan, et al.. (2020). Effects of a Central Atom and Peripheral Substituents on Photoinduced Electron Transfer in the Phthalocyanine–Fullerene Donor–Acceptor Solution-Processable Dyads. The Journal of Physical Chemistry C. 124(7). 4010–4023.
17.
Ksenofontov, Alexander A., et al.. (2020). Non-covalent supramolecular systems with photoinduced electron transfer based on zinc bis(dipyrromethenate)s and C60. Dyes and Pigments. 185. 108918–108918.
18.
Бичан, Н. Г., Е. Н. Овченкова, Arshak A. Tsaturyan, & Т. Н. Ломова. (2020). Spectral properties of supramolecular systems based on cobalt(ii )/manganese(iii ) phthalocyanine and fullero[60]pyrrolidines with PET. New Journal of Chemistry. 44(26). 11262–11270.
19.
Бичан, Н. Г., Е. Н. Овченкова, N.O. Kudryakova, et al.. (2018). Self-assembled cobalt(ii )porphyrin–fulleropyrrolidine triads via axial coordination with photoinduced electron transfer. New Journal of Chemistry. 42(15). 12449–12456.
20.
Бичан, Н. Г., et al.. (2018). Formation reaction and chemical structure of a novel supramolecular triade based on cobalt(II) 5,10,15,20-(tetra-4-tert-butylphenyl)-21H,23H-porphyrin and 1-methyl-2-(pyridin-4'-yl)-3,4-fullero[60]pyrrolidine. Журнал структурной химии. 59(3).
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