Aza boron-pyridyl-isoindoline isomers: Synthesis and photophysical properties

Hui Liu, Yanping Wu, Zhifang Li, Hua Lu

研究成果: Article査読

6 被引用数 (Scopus)

抄録

By changing benzo-fused position on pyridyl unit, three aza boron-pyridyl-isoindoline isomers, a new type of BODIPY analog, are synthesized through a facile two step reaction. These isomers show broad envelopes of intense vibrational bands in the absorption and emission spectra with moderate fuorescence quantum yields. In comparison to those of classical BODIPYs, signifcant fuorescence intensity are observed for these isomers in flm and powder. An analysis of the structureproperty relationships has been carried out based on X-ray crystallography, optical spectroscopy, and theoretical calculation.

本文言語English
ページ(範囲)679-685
ページ数7
ジャーナルJournal of Porphyrins and Phthalocyanines
18
DOI
出版ステータスPublished - 2014 8

ASJC Scopus subject areas

  • 化学 (全般)

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