Výsledky vyhledávání - "A. I. Poddel'sky"

Akademický článek

Synthesis, electrochemical properties, and antioxidant activity of sterically hindered catechols with 1,3,4-oxadiazole, 1,2,4-triazole, thiazole or pyridine fragments

Autor: Daria A. Burmistrova, Andrey Galustyan, Nadezhda P. Pomortseva, Kristina D. Pashaeva, Maxim V. Arsenyev, Oleg P. Demidov, Mikhail A. Kiskin, Andrey I. Poddel’sky, Nadezhda T. Berberova, Ivan V. Smolyaninov

Publikováno v: Beilstein Journal of Organic Chemistry, Vol 20, Iss 1, Pp 2378-2391 (2024)

A series of new RS−, RS−CH2− and R2N−CH2-functionalized сatechols with heterocyclic fragments such as 1,3,4-oxadiazole, 1,2,4-triazole, thiazole, or pyridine were synthesized by the reaction of 3,5-di-tert-butyl-o-benzoquinone or 3,5-di-tert

Externí odkaz: https://doaj.org/article/0e7cbdabb2fe425c9582c25afa879309

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Akademický článek

Imine-Based Catechols and o‑Benzoquinones: Synthesis, Structure, and Features of Redox Behavior

Autor: Tatiana V. Astaf’eva, Maxim V. Arsenyev, Roman V. Rumyantcev, Georgy K. Fukin, Vladimir K. Cherkasov, Andrey I. Poddel’sky

Publikováno v: ACS Omega, Vol 5, Iss 35, Pp 22179-22191 (2020)

Externí odkaz: https://doaj.org/article/7bc9e02f557a446db7b354a16817d277

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Akademický článek

Low-Coordinate Mixed Ligand NacNac Complexes of Rare Earth Metals

Autor: Svetlana V. Klementyeva, Taisiya S. Sukhikh, Pavel A. Abramov, Andrey I. Poddel’sky

Publikováno v: Molecules, Vol 28, Iss 4, p 1994 (2023)

We report the synthesis and characterization of two types of new mixed-ligand rare earth complexes: tetracoordinate (NacNacMes)Ln(BIANdipp) (Ln = Dy (1), Er (2) and Y (3)) and pentacoordinate (NacNacMes)Ln(APdipp)(THF) (Ln = Dy (4), Er (5) and Y (6))

Externí odkaz: https://doaj.org/article/257f42aa7f7d47ecabe5758b60da5c1f

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Akademický článek

Heteroligand α-Diimine-Zn(II) Complexes with O,N,O′- and O,N,S-Donor Redox-Active Schiff Bases: Synthesis, Structure and Electrochemical Properties

Autor: Ivan V. Smolyaninov, Andrey I. Poddel’sky, Daria A. Burmistrova, Julia K. Voronina, Nadezhda P. Pomortseva, Vasiliy A. Fokin, Ekaterina D. Tselukovskaya, Ivan V. Ananyev, Nadezhda T. Berberova, Igor L. Eremenko

Publikováno v: Molecules, Vol 27, Iss 23, p 8216 (2022)

A number of novel heteroligand Zn(II) complexes (1–8) of the general type (Ln)Zn(NN) containing O,N,O′-, O,N,S-donor redox-active Schiff bases and neutral N,N′-chelating ligands (NN) were synthesized. The target Schiff bases LnH2 were obtained

Externí odkaz: https://doaj.org/article/481e4fd7f9fa47aba9e87303b2d31754

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Akademický článek

Binuclear Triphenylantimony(V) Catecholates through N-Donor Linkers: Structural Features and Redox Properties

Autor: Andrey I. Poddel’sky, Ivan V. Smolyaninov, Aleksandra I. Shataeva, Evgenii V. Baranov, Georgy K. Fukin

Publikováno v: Molecules, Vol 27, Iss 19, p 6484 (2022)

A series of binuclear triphenylantimony(V) bis-catecholato complexes 1–11 of the type (Cat)Ph3Sb-linker-SbPh3(Cat) was prepared by a reaction of the corresponding mononuclear catecholates (Cat)SbPh3 with a neutral bidentate donor linker ligands pyr

Externí odkaz: https://doaj.org/article/df2e39ad209949fbbdfed8f5d762bba2

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Akademický článek

Heteroligand Metal Complexes with Extended Redox Properties Based on Redox-Active Chelating Ligands of o-Quinone Type and Ferrocene

Autor: Svetlana V. Baryshnikova, Andrey I. Poddel’sky

Publikováno v: Molecules, Vol 27, Iss 12, p 3928 (2022)

A combination of different types of redox-active systems in one molecule makes it possible to create coordination compounds with extended redox abilities, combining molecular and electronic structures determined by the features of intra- and intermol

Externí odkaz: https://doaj.org/article/f1fd82023af54ddab9e60118d63250c2

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Akademický článek

Synthesis and Antioxidant Activity of New Catechol Thioethers with the Methylene Linker

Autor: Ivan V. Smolyaninov, Daria A. Burmistrova, Maxim V. Arsenyev, Maria A. Polovinkina, Nadezhda P. Pomortseva, Georgy K. Fukin, Andrey I. Poddel’sky, Nadezhda T. Berberova

Publikováno v: Molecules, Vol 27, Iss 10, p 3169 (2022)

Novel catechol thio-ethers with different heterocyclic substituents at sulfur atom were prepared by reacting 3,5-di-tert-butyl-6-methoxymethylcatechol with functionalized thiols under acidic conditions. A common feature of compounds is a methylene br

Externí odkaz: https://doaj.org/article/a0a3c71aff694d73afb6a348d2e6d76d

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