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Photophysical properties and application in live cell imaging of B,B-fluoro-perfluoroalkyl BODIPYs.


ABSTRACT: The photophysical properties of newly identified B,B-fluoro-perfluoroalkyl BODIPYs (2 and 3), which possess a fluoro group and a trifluoromethyl or pentafluoroethyl group at the boron center, were investigated. B,B-Fluoro-perfluoroalkyl BODIPYs 2 and 3 exhibited better photophysical/chemical properties than B,B-difluoro-BODIPY 1, as follows: (1) higher photostability both in methanol solvent and in a live cell environment, (2) higher stability against acid degradation, and (3) improved fluorescence signal-to-noise ratios in a cell system. These favorable properties of B,B-fluoro-perfluoroalkyl BODIPYs are likely due to the highly electron-withdrawing nature of the perfluoroalkyl groups on the boron atom, which reduces the reactivity to 1O2 and strengthens the complexation of the dipyrromethene ligands to the boron atom. Thus, B,B-fluoro perfluoroalkyl BODIPYs may be useful functional molecules for various applications.

SUBMITTER: Taniguchi A 

PROVIDER: S-EPMC6657624 | biostudies-literature | 2019 Jul

REPOSITORIES: biostudies-literature

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Photophysical properties and application in live cell imaging of B,B-fluoro-perfluoroalkyl BODIPYs.

Taniguchi Atsuhiko A   Sawazaki Taka T   Shimizu Yusuke Y   Sohma Youhei Y   Kanai Motomu M  

MedChemComm 20190316 7


The photophysical properties of newly identified B,B-fluoro-perfluoroalkyl BODIPYs (<b>2</b> and <b>3</b>), which possess a fluoro group and a trifluoromethyl or pentafluoroethyl group at the boron center, were investigated. B,B-Fluoro-perfluoroalkyl BODIPYs <b>2</b> and <b>3</b> exhibited better photophysical/chemical properties than B,B-difluoro-BODIPY <b>1</b>, as follows: (1) higher photostability both in methanol solvent and in a live cell environment, (2) higher stability against acid degr  ...[more]

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