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Synthesis of polyimide oligomer attached with hemicyanine dye
Author(s) -
Qin Chuanxiang,
Wang Jianjun,
Li Yi,
Xie Hongde,
Wang Xinbo,
Dai Lixing,
Wang Xiaomei,
Chen Guoqiang
Publication year - 2009
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.29961
Subject(s) - polyimide , oligomer , tetraphenylborate , polymer chemistry , dimethylformamide , solvent , polymer , chemistry , condensation polymer , materials science , organic chemistry , ion , layer (electronics)
Two hemicyanine dyes, trans‐4‐[ p ‐( N,N ‐di(2‐hydroxyethyl)) amino‐styryl]‐ N ‐methylpyridinium tetraphenylborate (dye‐C 1 ) and trans‐4‐[ p ‐( N,N ‐di(2‐hydroxyethyl)) amino‐styryl]‐ N ‐octylpyridinium tetraphenylborate (dye‐C 8 ) were synthesized, and characterized by infrared, 1 H‐NMR, thermoanalysis, respectively. Then polyimide (PI) oligomers (referred to as P‐C 1 and P‐C 8 ) with these hemicyanine dyes attached to the polymer side chain were prepared through Mitsunobu condensation. When the linear optical properties of the two dyes and the two PI oligomers were studied in dimethylformamide solvent, there were obvious blue shifts in the spectra of the oligomers. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009

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