V. V. Kurdyukov

445 total citations
32 papers, 368 citations indexed

About

V. V. Kurdyukov is a scholar working on Materials Chemistry, Physical and Theoretical Chemistry and Organic Chemistry. According to data from OpenAlex, V. V. Kurdyukov has authored 32 papers receiving a total of 368 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Materials Chemistry, 18 papers in Physical and Theoretical Chemistry and 11 papers in Organic Chemistry. Recurrent topics in V. V. Kurdyukov's work include Porphyrin and Phthalocyanine Chemistry (19 papers), Photochemistry and Electron Transfer Studies (17 papers) and Photochromic and Fluorescence Chemistry (8 papers). V. V. Kurdyukov is often cited by papers focused on Porphyrin and Phthalocyanine Chemistry (19 papers), Photochemistry and Electron Transfer Studies (17 papers) and Photochromic and Fluorescence Chemistry (8 papers). V. V. Kurdyukov collaborates with scholars based in Ukraine, Germany and United States. V. V. Kurdyukov's co-authors include А. И. Толмачев, Wolfgang Rettig, А. I. Tolmachev, Marina L. Dekhtyar, Oleg Dimitriev, A.D. Kachkovski, Davorin Peceli, Eric W. Van Stryland, Honghua Hu and David J. Hagan and has published in prestigious journals such as The Journal of Physical Chemistry B, Chemical Communications and Physical Chemistry Chemical Physics.

In The Last Decade

V. V. Kurdyukov

29 papers receiving 361 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
V. V. Kurdyukov Ukraine 10 256 146 78 75 59 32 368
А. С. Старухин Belarus 10 374 1.5× 169 1.2× 60 0.8× 44 0.6× 50 0.8× 57 444
Andriy O. Gerasov Ukraine 10 411 1.6× 163 1.1× 189 2.4× 79 1.1× 70 1.2× 14 529
Joscha Hoche Germany 10 292 1.1× 130 0.9× 64 0.8× 83 1.1× 131 2.2× 13 460
Els Braeken Belgium 6 250 1.0× 93 0.6× 98 1.3× 54 0.7× 90 1.5× 7 423
Cloé Azarias France 14 381 1.5× 261 1.8× 56 0.7× 169 2.3× 129 2.2× 23 542
Л. Л. Гладков Belarus 10 279 1.1× 101 0.7× 35 0.4× 41 0.5× 29 0.5× 60 354
Ulrich Rösch Germany 5 405 1.6× 99 0.7× 50 0.6× 130 1.7× 86 1.5× 5 548
И. А. Михайлов United States 11 277 1.1× 100 0.7× 146 1.9× 67 0.9× 36 0.6× 16 383
R.B.M. Koehorst Netherlands 10 310 1.2× 110 0.8× 40 0.5× 50 0.7× 120 2.0× 17 411
O.D. Kachkovsky Ukraine 14 392 1.5× 139 1.0× 205 2.6× 184 2.5× 62 1.1× 83 630

Countries citing papers authored by V. V. Kurdyukov

Since Specialization
Citations

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

Fields of papers citing papers by V. V. Kurdyukov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by V. V. Kurdyukov. 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 V. V. Kurdyukov. The network helps show where V. V. Kurdyukov may publish in the future.

Co-authorship network of co-authors of V. V. Kurdyukov

This figure shows the co-authorship network connecting the top 25 collaborators of V. V. Kurdyukov. A scholar is included among the top collaborators of V. V. Kurdyukov 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 V. V. Kurdyukov. V. V. Kurdyukov 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.
Kurdyukov, V. V., et al.. (2022). Bis-dicyanomethylene substituted indosquaraine: Synthesis, spectral properties, molecular and crystal structure. Journal of Molecular Structure. 1271. 134038–134038. 2 indexed citations
2.
Dmytruk, Andriy, et al.. (2021). Excited state relaxation in cationic pentamethine cyanines studied by time-resolved spectroscopy. Dyes and Pigments. 193. 109539–109539.
3.
Kulinich, Andrii V., V. V. Kurdyukov, & A. A. Ishchenko. (2019). Effect of bulky substituents in the donor and acceptor terminal groups on solvatochromism of Brooker's merocyanine. New Journal of Chemistry. 43(19). 7379–7385. 13 indexed citations
4.
Kurdyukov, V. V., et al.. (2019). Isomeric Bisdicyanomethylene-Substituted 1,3- and 1,2-Pyrilo-4-squaraines: Synthesis, Molecular, and Crystal Structure. Russian Journal of General Chemistry. 89(2). 212–218. 1 indexed citations
5.
Piryatinskiĭ, Yu. P., et al.. (2018). Suppression of Kasha’s rule in higher excited states of 4-pyrilocyanines. Molecular Crystals and Liquid Crystals. 672(1). 33–40. 2 indexed citations
6.
Dmytrenko, О. P., et al.. (2017). Spectral and Quantum-Chemical Studies of the Band Shape in Absorption of Merocyanine Derivatives of Cyclohexadienone. Journal of Advanced Physics. 6(4). 514–523.
7.
Letrun, Romain, Marius Koch, Marina L. Dekhtyar, et al.. (2013). Ultrafast Excited-State Dynamics of Donor–Acceptor Biaryls: Comparison between Pyridinium and Pyrylium Phenolates. The Journal of Physical Chemistry A. 117(49). 13112–13126. 32 indexed citations
8.
Толмачев, А. И., et al.. (2013). Synthesis, molecular, and crystal structure of 3,4-bis[(2,6-di-tert-butyl-4H-pyran-4-ylidene)methyl]cyclobut-3-ene-1,2-dione and -1,2-dithione. Russian Journal of General Chemistry. 83(11). 2088–2094. 2 indexed citations
9.
Rettig, Wolfgang, Marina L. Dekhtyar, А. И. Толмачев, & V. V. Kurdyukov. (2012). Two heterocyclic merocyanine classes and their optical properties in relation to the donor-acceptor strength of end substituents. Chemistry of Heterocyclic Compounds. 47(10). 1244–1257. 14 indexed citations
10.
Peceli, Davorin, Scott Webster, Dmitry A. Fishman, et al.. (2012). Optimization of the Double Pump–Probe Technique: Decoupling the Triplet Yield and Cross Section. The Journal of Physical Chemistry A. 116(20). 4833–4841. 10 indexed citations
11.
Bricks, J.L., et al.. (2011). Conformational analysis of polymethine dyes derived from the 2-azaazulene. Journal of Molecular Structure. 1007. 52–62. 3 indexed citations
12.
Peceli, Davorin, Scott Webster, Dmitry A. Fishman, et al.. (2011). Advance in Double Pump-Probe Technique for Triplet Quantum Yield Determination. Journal of International Crisis and Risk Communication Research. 71. CTuY4–CTuY4. 1 indexed citations
13.
García-Acosta, Beatriz, María Comes, J.L. Bricks, et al.. (2006). Sensory hybrid host materials for the selective chromo-fluorogenic detection of biogenic amines. Chemical Communications. 2239–2241. 61 indexed citations
14.
Kachkovsky, O.D., et al.. (2005). Electronic properties of polymethine systems. 10. Electron structure and absorption spectra of cyanine bases. Dyes and Pigments. 70(3). 212–219. 12 indexed citations
15.
Yarmoluk, S. M., et al.. (2002). Interaction of cyanine dyes with nucleic acids. New (pyrido)(thio)trimethincyanine dye CCyan 40 for fluorescent labeling of oligonucleotides. Biopolymers and Cell. 18(4). 340–346. 2 indexed citations
16.
Rettig, Wolfgang, et al.. (2001). The role of internal twisting in the photophysics of stilbazolium dyes. Physical Chemistry Chemical Physics. 3(17). 3555–3561. 26 indexed citations
17.
Kachkovski, A.D., et al.. (2000). Nature of the absorption bands of pyrylocyanines.2. Influence of t-Bu, Ph and Th ring substituents. Dyes and Pigments. 45(1). 1–7. 5 indexed citations
18.
Толмачев, А. И., et al.. (2000). Molecular and crystal structure of pyrylium squarylium dyes. Journal of Structural Chemistry. 41(4). 640–645. 2 indexed citations
19.
Ishchenko, A. A., et al.. (1992). Conformational structure of pyrylo-2-monomethinecyanine and its thio analogs. Journal of Structural Chemistry. 33(1). 117–122. 1 indexed citations
20.
Kurdyukov, V. V., et al.. (1987). Pyrilocyanines. 24. Symmetrical tetra-tert-butyl substituted pyrilo-2-cyanines. Chemistry of Heterocyclic Compounds. 23(6). 628–633. 3 indexed citations

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