Conformation-Restricted Partially and Fully Fused BODIPY Dimers as Highly Stable Near-Infrared Fluorescent Dyes
Author(s) -
Jun Wang,
Qinghua Wu,
Shaowu Wang,
Changjiang Yu,
Jin Li,
Erhong Hao,
Yun Wei,
Xiaolong Mu,
Lijuan Jiao
Publication year - 2015
Publication title -
organic letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.94
H-Index - 239
eISSN - 1523-7060
pISSN - 1523-7052
DOI - 10.1021/acs.orglett.5b02717
Subject(s) - bodipy , chemistry , fluorescence , photochemistry , benzene , density functional theory , condensation , absorption (acoustics) , monomer , molecule , infrared , electrochemistry , near infrared spectroscopy , computational chemistry , polymer , materials science , organic chemistry , optics , physics , electrode , composite material , thermodynamics
A set of highly stable conformation-restricted partially and fully fused BODIPY dimers (α,β-cyclohexadiene-fused and α,β-benzene-fused dimers) were synthesized from a one-pot condensation of 2-formylpyrroles with α,β-cyclohexadiene-fused bipyrrole 3. Effective expansion of π-conjugation over these fused BODIPY dimers was observed by X-ray analysis, density functional theory (DFT) calculations, and electrochemical and optical measurements, as demonstrated by their strong absorption and emissions in the near-infrared (NIR) range (650 to 820 nm).
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