1,7-isoxazolyl Substituted BODIPY Dyes – Synthesis and Photophysical Properties

A range of novel BODIPYs with the isoxazolyl groups at 1,7-positions were prepared from 3-(4-chlorophenyl)-5-(5-phenyl-1H-pyrrol-3-yl)isoxazole and their photophysical properties were characterized. The presence of the isoxazolyl groups at 1,7-positions, shifts long-wavelength absorption at 581±4 nm and emission at 622±3 nm in the near-infrared region. A comparison of three variants of substituents at positions 1,7 of BODIPY core is shown. © 2023 Wiley-VCH GmbH.

Авторы
Matveeva M.D. , Zheleznova T.Y. , Kostyuchenko A.S. , Miftyakhova A.R. , Zhilyaev D.I. , Voskressensky L.G. , Talarico G. , Efimov I.V.
Журнал
Издательство
Wiley-Blackwell
Номер выпуска
5
Язык
Английский
Статус
Опубликовано
Номер
e202204465
Том
8
Год
2023
Организации
  • 1 A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Moscow, 119991, Russian Federation
  • 2 Laboratory of New Organic Materials, Omsk State Technical University, Mira Ave. 11, Omsk, 644050, Russian Federation
  • 3 Research Center: Molecular Design and Synthesis of Innovative Compounds for Medicine, Peoples' Friendship University of Russia (RUDN University), Miklukho-Maklaya st, 6, Moscow, 117198, Russian Federation
  • 4 Dipartimento di Scienze Chimiche, Università di Napoli Federico II, Via Cintia, Napoli, 80124, Italy
Ключевые слова
BODIPY; Boron; Cyclization; Fluorophores; Pyrroles
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