Gleb Morozkov

Gleb Morozkov

orcid

Research Focus & Metrics

Academic Career Length

5Years (2022-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 June 2022 in Dalton Transactions
Verified
Journal Article
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GMGleb Morozkov
Gleb Morozkov
AAAnton Abel
Anton Abel
MFMikhail A. Filatov
Mikhail A. Filatov
SNSergei E. Nefedov
Sergei E. Nefedov
VRVitaly Roznyatovsky
Vitaly Roznyatovsky
Alla Bessmertnykh-LemeuneAlla Bessmertnykh-Lemeune
Alla Bessmertnykh-Lemeune
[Ru(phen)(bpy) 2 ] 2+ -type complexes with a P(O)(OEt) 2 -substituted phen ligand are efficient photocatalysts for photoreactions proceeding via the electron transfer and energy transfer pathways.

21 November 2023 in Dalton Transactions
Verified
Journal Article
Closed access
PDF file
GMGleb Morozkov
Gleb Morozkov
AAAnton Abel
Anton Abel
KLKonstantin Lyssenko
Konstantin Lyssenko
VRVitaly Roznyatovsky
Vitaly Roznyatovsky
AAAlexei Averin
Alexei Averin
Alla Bessmertnykh-LemeuneAlla Bessmertnykh-Lemeune
Alla Bessmertnykh-Lemeune
Ru(ii) complexes with phosphonate-substituted phenanthroline ligands exhibited higher efficiency than the benchmark photocatalyst [Ru(bpy)3]2+ in photoredox-catalyzed reactions and could be recycled through water extraction for reuse.

25 November 2024 in Molecules
Verified
Journal Article
Open access
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GMGleb Morozkov
Gleb Morozkov
ATArtem A. Troickiy
Artem A. Troickiy
AAAlexei Averin
Alexei Averin
AMAlexander Yu. Mitrofanov
Alexander Yu. Mitrofanov
AAAnton Abel
Anton Abel
Irina Petrovna  BeletskayaIrina Petrovna Beletskaya
Irina Petrovna Beletskaya
Photoredox-catalyzed phosphonylation of bromo-substituted 1,10-phenanthrolines under visible light irradiation was studied. The reaction was shown to proceed under mild conditions with Eosin Y as a photocatalyst in DMSO under blue light irradiation. It is transition-metal-free and affords the target phosphonate-substituted 1,10-phenanthrolines in moderate yields (26–51%) in 22 to 40 h. The rate and selectivity of the reaction depend largely on the position of the bromine atom, as well as on the nature and position of other substituents in the 1,10-phenanthroline core.