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N‐Substituted Dicyanomethylphenyl Radicals: Dynamic Covalent Properties and Formation of Stimuli‐Responsive Cyclophanes by Self‐Assembly
Author(s) -
Kobashi Toshiyuki,
Sakamaki Daisuke,
Seki Shu
Publication year - 2016
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.201603409
Subject(s) - diradical , covalent bond , radical , triphenylamine , dynamic covalent chemistry , carbazole , chemistry , dimer , monomer , photochemistry , bond cleavage , polymer chemistry , supramolecular chemistry , molecule , organic chemistry , polymer , physics , nuclear physics , singlet state , catalysis , excited state
Dynamic covalent bonds and their chemistry have been of particular interest both from a fundamental and materials science aspect. Demonstrated herein is that triphenylamine (TPA) and carbazole (Cz), substituted with a dicyanomethyl radical, are useful motifs for dynamic covalent chemistry as they have the appropriate bond strength between monomer units as well as high stability and synthetic simplicity. TPA and Cz units substituted by two dicyanomethyl radicals formed macrocyclic oligomers classified as novel types of azacyclophanes, and in particular, the TPA‐based diradical gave a cyclic dimer in almost quantitative yield. The cyclic oligomers exhibited thermo‐ and mechanochromic behavior resulting from the generation of radical species by intermonomer C−C bond cleavage.