1,7‐isoxazolyl Substituted BODIPY Dyes – Synthesis and Photophysical Properties-Reference-Cited by-同舟云学术

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

Published:2023-02 Issue:5 Volume:8 Page:
ISSN:2365-6549
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Author:

Matveeva Maria D.¹^ORCID,Zheleznova Tatyana Yu.²^ORCID,Kostyuchenko Anastasia S.²^ORCID,Miftyakhova Almira R.³^ORCID,Zhilyaev Dmitry I.³^ORCID,Voskressensky Leonid G.³^ORCID,Talarico Giovanni⁴^ORCID,Efimov Ilya V.³^ORCID

Affiliation:

1. A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences 119991 Moscow Russia

2. Laboratory of New Organic Materials Omsk State Technical University 644050 Omsk, Mira Ave. 11 Russia

3. Research Center: Molecular Design and Synthesis of Innovative Compounds for Medicine Peoples' Friendship University of Russia (RUDN University) 117198, Russia Moscow, Miklukho-Maklaya st, 6 Russia

4. Dipartimento di Scienze Chimiche Università di Napoli Federico II, Via Cintia 80124 Napoli Italy

Abstract

AbstractA 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.

Funder

Russian Foundation for Basic Research

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.202204465

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