期刊
CHEMISTRY LETTERS
卷 52, 期 5, 页码 354-357出版社
CHEMICAL SOC JAPAN
DOI: 10.1246/cl.230072
关键词
Rigid pi-electron system; Thioindigo; Carbazole
A new class of rigid and planar compounds, carbazole-fused thioindigo oligomers (Cz(n)TI(n)11, n = 2, 3), was synthesized via palladium-catalyzed carbon-sulfur bond formation and intramolecular Friedel-Crafts acylation. The study focused on the reaction conditions for thioindigo moiety formation and the photoelectrochemical properties of the oligomers, including their photochromic behavior.
A new class of rigid and planar compounds, carbazole-fused thioindigo oligomers (Cz(n)TI(n)11, n = 2, 3), was prepared using palladium-catalyzed carbon -sulfur bond formation and intramolecular Friedel-Crafts acylation as the key reactions. The reaction conditions for the formation of the thioindigo moiety, as well as the basic photo-and electrochemical prop-erties of the oligomers, including photochromic behavior, were investigated.
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