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Halochromic Phenolate Perylene Bisimides with Unprecedented NIR Spectroscopic Properties
Author(s) -
Lin MeiJin,
Fimmel Benjamin,
Radacki Krzysztof,
Würthner Frank
Publication year - 2011
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201105129
Subject(s) - perylene , steric effects , photochemistry , absorption (acoustics) , nucleophile , transition metal , ion , metal ions in aqueous solution , chemistry , nucleophilic substitution , carbon fibers , metal , catalysis , materials science , organic chemistry , molecule , composite number , composite material
CC coupling of 1,7‐dibromoperylene bisimide with sterically hindered 2,6‐di‐ tert ‐butylphenol by a carbon nucleophilic substitution reaction in the absence of transition‐metal catalysts gave novel halochromic perylene bisimides (see picture). The corresponding phenolate ions of these compounds exhibit unprecedented NIR spectroscopic properties including strong absorption with maxima at around 1200 nm.

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