Synthesis and photophysical properties of novel oxadiazole substituted BODIPY fluorophores

Maria D. Matveeva; Dmitry I. Zhilyaev; Almira R. Miftyakhova; Pavel Chulkin; Patryk Janasik; Leonid G. Voskressensky; Giovanni Talarico; Ilya V. Efimov

doi:10.1039/d1nj05317e

Synthesis and photophysical properties of novel oxadiazole substituted BODIPY fluorophores

Maria D. Matveeva
, Dmitry I. Zhilyaev
, Almira R. Miftyakhova
, Pavel Chulkin
, Patryk Janasik
, Leonid G. Voskressensky
, Giovanni Talarico
, Ilya V. Efimov

Russian Academy of Sciences
People's Friendship University of Russia
University of Naples Federico II

Research output: Contribution to journal › Article › peer-review

5 Citations (Scopus)

Abstract

Using 3-phenyl-5-(5-phenyl-1H-pyrrol-3-yl)-1,2,4-oxadiazole, BODIPYs with the oxadiazole groups at the 1,7-positions were prepared and their photophysical properties were characterized. The method employs 2,4-diphenyl substituted pyrrole and various aromatic aldehydes under solvent-free conditions. Due to the attachment of the oxadiazole groups at the 1,7-positions, the BODIPYs show long-wavelength absorption and emission in the near-infrared region.

Original language	English
Pages (from-to)	5725-5729
Number of pages	5
Journal	New Journal of Chemistry
Volume	46
Issue number	12
DOIs	https://doi.org/10.1039/d1nj05317e
Publication status	Published - 9 Feb 2022

ASJC Scopus subject areas

Catalysis
General Chemistry
Materials Chemistry

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title = "Synthesis and photophysical properties of novel oxadiazole substituted BODIPY fluorophores",

abstract = "Using 3-phenyl-5-(5-phenyl-1H-pyrrol-3-yl)-1,2,4-oxadiazole, BODIPYs with the oxadiazole groups at the 1,7-positions were prepared and their photophysical properties were characterized. The method employs 2,4-diphenyl substituted pyrrole and various aromatic aldehydes under solvent-free conditions. Due to the attachment of the oxadiazole groups at the 1,7-positions, the BODIPYs show long-wavelength absorption and emission in the near-infrared region.",

author = "Matveeva, \{Maria D.\} and Zhilyaev, \{Dmitry I.\} and Miftyakhova, \{Almira R.\} and Pavel Chulkin and Patryk Janasik and Voskressensky, \{Leonid G.\} and Giovanni Talarico and Efimov, \{Ilya V.\}",

note = "Publisher Copyright: {\textcopyright} 2022 The Royal Society of Chemistry",

year = "2022",

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day = "9",

doi = "10.1039/d1nj05317e",

language = "English",

volume = "46",

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publisher = "Royal Society of Chemistry",

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TY - JOUR

T1 - Synthesis and photophysical properties of novel oxadiazole substituted BODIPY fluorophores

AU - Matveeva, Maria D.

AU - Zhilyaev, Dmitry I.

AU - Miftyakhova, Almira R.

AU - Chulkin, Pavel

AU - Janasik, Patryk

AU - Voskressensky, Leonid G.

AU - Talarico, Giovanni

AU - Efimov, Ilya V.

PY - 2022/2/9

Y1 - 2022/2/9

N2 - Using 3-phenyl-5-(5-phenyl-1H-pyrrol-3-yl)-1,2,4-oxadiazole, BODIPYs with the oxadiazole groups at the 1,7-positions were prepared and their photophysical properties were characterized. The method employs 2,4-diphenyl substituted pyrrole and various aromatic aldehydes under solvent-free conditions. Due to the attachment of the oxadiazole groups at the 1,7-positions, the BODIPYs show long-wavelength absorption and emission in the near-infrared region.

AB - Using 3-phenyl-5-(5-phenyl-1H-pyrrol-3-yl)-1,2,4-oxadiazole, BODIPYs with the oxadiazole groups at the 1,7-positions were prepared and their photophysical properties were characterized. The method employs 2,4-diphenyl substituted pyrrole and various aromatic aldehydes under solvent-free conditions. Due to the attachment of the oxadiazole groups at the 1,7-positions, the BODIPYs show long-wavelength absorption and emission in the near-infrared region.

UR - https://www.scopus.com/pages/publications/85127198382

U2 - 10.1039/d1nj05317e

DO - 10.1039/d1nj05317e

M3 - Article

AN - SCOPUS:85127198382

SN - 1144-0546

VL - 46

SP - 5725

EP - 5729

JO - New Journal of Chemistry

JF - New Journal of Chemistry

IS - 12

ER -

Synthesis and photophysical properties of novel oxadiazole substituted BODIPY fluorophores

Abstract

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