Е. Н. Шепеленко

616 total citations
94 papers, 473 citations indexed

About

Е. Н. Шепеленко is a scholar working on Materials Chemistry, Organic Chemistry and Spectroscopy. According to data from OpenAlex, Е. Н. Шепеленко has authored 94 papers receiving a total of 473 indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Materials Chemistry, 59 papers in Organic Chemistry and 38 papers in Spectroscopy. Recurrent topics in Е. Н. Шепеленко's work include Photochromic and Fluorescence Chemistry (45 papers), Molecular Sensors and Ion Detection (36 papers) and Luminescence and Fluorescent Materials (19 papers). Е. Н. Шепеленко is often cited by papers focused on Photochromic and Fluorescence Chemistry (45 papers), Molecular Sensors and Ion Detection (36 papers) and Luminescence and Fluorescent Materials (19 papers). Е. Н. Шепеленко collaborates with scholars based in Russia, Belarus and Israel. Е. Н. Шепеленко's co-authors include В. А. Брень, Владимир И. Минкин, А. Д. Дубоносов, Г. С. Бородкин, А. В. Метелица, Nadezhda I. Makarova, L. Yu. Ukhin, А. Г. Стариков, T. N. Gribanova and B. S. Lukyanov and has published in prestigious journals such as Tetrahedron, Tetrahedron Letters and Journal of Photochemistry and Photobiology A Chemistry.

In The Last Decade

Е. Н. Шепеленко

88 papers receiving 458 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Е. Н. Шепеленко Russia 12 278 276 187 78 42 94 473
Daria V. Berdnikova Germany 15 240 0.9× 273 1.0× 140 0.7× 82 1.1× 146 3.5× 42 503
Anatoly V. Chernyshev Russia 13 239 0.9× 461 1.7× 128 0.7× 294 3.8× 52 1.2× 75 592
Srinivasan Rajagopal Canada 7 170 0.6× 149 0.5× 74 0.4× 45 0.6× 64 1.5× 11 416
Peter Czerney Germany 16 297 1.1× 236 0.9× 104 0.6× 32 0.4× 61 1.5× 44 583
Shuna Sun China 11 95 0.3× 271 1.0× 193 1.0× 31 0.4× 200 4.8× 20 520
Mikhail Yu. Ievlev Russia 15 428 1.5× 295 1.1× 113 0.6× 34 0.4× 56 1.3× 78 646
Olena Vakuliuk Poland 15 357 1.3× 328 1.2× 82 0.4× 19 0.2× 50 1.2× 36 684
Meijiao Cao China 11 133 0.5× 359 1.3× 336 1.8× 61 0.8× 104 2.5× 11 585
Zeus A. De los Santos United States 13 232 0.8× 115 0.4× 260 1.4× 19 0.2× 114 2.7× 20 494
Seyma Ozturk United States 8 225 0.8× 229 0.8× 188 1.0× 22 0.3× 102 2.4× 11 484

Countries citing papers authored by Е. Н. Шепеленко

Since Specialization
Citations

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

Fields of papers citing papers by Е. Н. Шепеленко

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Е. Н. Шепеленко. 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 Е. Н. Шепеленко. The network helps show where Е. Н. Шепеленко may publish in the future.

Co-authorship network of co-authors of Е. Н. Шепеленко

This figure shows the co-authorship network connecting the top 25 collaborators of Е. Н. Шепеленко. A scholar is included among the top collaborators of Е. Н. Шепеленко 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 Е. Н. Шепеленко. Е. Н. Шепеленко 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.
Шепеленко, Е. Н., et al.. (2024). Coumarinyl(pyrrolyl)ethenes for the detection of Pd2+, CN− and F− ions, test strips based on them and logic gates. Tetrahedron. 159. 134012–134012. 3 indexed citations
2.
Ukhin, L. Yu., et al.. (2023). New reactions of 2,3-diaminonaphthaline with carbonyl electrophiles. Mendeleev Communications. 33(1). 115–117.
3.
Шепеленко, Е. Н., Л. Д. Попов, Т. М. Валова, et al.. (2023). Bifunctional photo- and ionochromic hybrids of indolyl(thienyl) diarylethenes and rhodamine. Journal of Photochemistry and Photobiology A Chemistry. 448. 115310–115310. 1 indexed citations
4.
Шепеленко, Е. Н., et al.. (2023). Rhodamine 6G-Based Molecular Ion-Active Switches of Optical and Fluorescent Properties. Russian Journal of General Chemistry. 93(8). 1989–1997.
5.
Шепеленко, Е. Н., et al.. (2023). Photo- and Ionochromic Diarylethenes with Receptor Fragments in the Thiazole Bridge. Russian Journal of General Chemistry. 93(2). 278–285. 1 indexed citations
6.
Попов, Л. Д., et al.. (2023). Synthesis, Spectral-Luminescent, and Ionochromic Properties of a Rhodamine B Derivative Containing a Terminal (4-Hydroxybenzyl)triphenylphosphonium Chloride Substituent. Russian Journal of General Chemistry. 93(3). 535–541. 1 indexed citations
7.
Шепеленко, Е. Н., et al.. (2023). Photo- and ionochromic diarylethenes containing tetrazolo[1,5-a]quinoline receptor groups in a thiazole bridge and their application in test strips. Chemistry of Heterocyclic Compounds. 59(8). 618–622. 2 indexed citations
8.
Шепеленко, Е. Н., et al.. (2022). Solvent-dependent selective “naked eye” chromofluorogenic multifunctional rhodamine-based probe for Al3+, Cu2+, Hg2+, S2− and CN− ions. Tetrahedron. 110. 132710–132710. 9 indexed citations
9.
Шепеленко, Е. Н., et al.. (2018). Photo- and ionochromic thienyl(coumarinyl)thiazoles. Journal of Molecular Structure. 1163. 221–226. 4 indexed citations
10.
Шепеленко, Е. Н., et al.. (2017). SYNTHESIS OF NOVEL NONSYMMETRIC DIHETARYLETHENES WITH 1,3-THIAZOLE BRIDGE. 13(3). 34–38. 1 indexed citations
11.
Шепеленко, Е. Н., Л. Д. Попов, А. Д. Дубоносов, et al.. (2017). Bifunctional terpyridine/ o -hydroxyimine chemosensors. Journal of Molecular Structure. 1154. 219–224. 3 indexed citations
12.
Ukhin, L. Yu., et al.. (2013). Synthesis of 6’ H-spiro(indene-2,2’ -[1,3]oxathiane)-1,3,5’ -triones. Mendeleev Communications. 23(6). 352–353. 5 indexed citations
13.
Шепеленко, Е. Н., et al.. (2012). New chemosensor systems of the benzo-[de]Isoquinoline-1,3-Dione Series. Chemistry of Heterocyclic Compounds. 48(9). 1325–1331. 2 indexed citations
14.
Ukhin, L. Yu., et al.. (2011). 2-Aminothiophene derivatives in a novel synthesis of phthalimidines. Russian Chemical Bulletin. 60(2). 352–360. 3 indexed citations
15.
Шепеленко, Е. Н., et al.. (2009). Chemosensors based on N-(2-aminophenyl)-N-(9-anthrylmethyl)amine: II. Russian Journal of Organic Chemistry. 45(2). 161–165. 5 indexed citations
16.
Дубоносов, А. Д., Владимир И. Минкин, В. А. Брень, et al.. (2008). Tautomeric crown-containing chemosensors for alkali-earth metal cations. Tetrahedron. 64(14). 3160–3167. 29 indexed citations
17.
Дубоносов, А. Д., et al.. (2001). Benzoid-Quinoid Tautomerism of Schiff Bases and Their Structural Analogs: LI. Photoacylotropic Enaminoketones with a Fluorophoric Migrant. Russian Journal of Organic Chemistry. 37(9). 1318–1322. 5 indexed citations
18.
Lukyanov, B. S., et al.. (2000). Novel indolinospiropyrans containing a condensed furan moiety. Chemistry of Heterocyclic Compounds. 36(7). 872–873.
19.
Брень, В. А., et al.. (1991). Photoisomerization of Hydrazones of 2-Acetyl-3-hydroxy-benzo[b]furan and -benzo[b]thiophene. Mendeleev Communications. 1(2). 72–73. 8 indexed citations
20.

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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