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Synthesis and characterization of organo‐soluble polyamides containing triaryl imidazole pendant and ether linkage moieties: thermal, photophysical, and chemiluminescent properties
Author(s) -
Ghaemy M.,
Nasab S. M. Amini
Publication year - 2011
Publication title -
polymers for advanced technologies
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.61
H-Index - 90
eISSN - 1099-1581
pISSN - 1042-7147
DOI - 10.1002/pat.1763
Subject(s) - polyamide , monomer , diamine , thermal stability , imidazole , polymer chemistry , solvatochromism , benzimidazole , ether , materials science , chemistry , organic chemistry , solvent , polymer
A new symmetrical diamine monomer containing a triaryl imidazole pendant group was successfully synthesized by the nucleophilic substitution of hydroquinone with the synthesized 2‐(2‐chloro‐5‐nitrophenyl)‐4, 5‐diphenyl‐1H‐imidazole (I). A series of novel polyamides were prepared from the diamine monomer and various aliphatic and aromatic dicarboxylic acids via phosphorylation polyamidation. These polyamides are readily soluble in many organic solvents; their inherent viscosities ranged from 0.68 to 0.89 dl/g and gave tough and flexible films by solution‐casting. They had useful levels of thermal stability associated with relatively high T g s (186–278°C), 10% weight loss temperatures in the range of 355–482°C, and char yields at 600°C in air up to 67%. All the polyamides have fluorescence emission in dilute (0.2 g/dl) DMAc solution with maxima at 425–495 nm and with the quantum yields in the range 14–28%. The chemiluminescence activity of polyamides was also studied in the presence of peroxyoxalate. Copyright © 2010 John Wiley & Sons, Ltd.