Novel family of triphenylamine-containing, hole-transporting, amorphous, aromatic polyamides with stable electrochromic properties

[[abstract]]We report the preparation and characterization of a series of novel electrochromic, aromatic poly(amine amide)s with pendent triphenylamine units. The synthesis proceeded via direct phosphorylation polycondensation between a novel diamine, N,N-bis(4-aminophenyl)-N',N'-diphenyl-1,4-phenylenediamine, and various aromatic dicarboxylic acids. All the poly(amine amide)s were amorphous and readily soluble in many common organic solvents and could be solution-cast into transparent, tough, and flexible films with good mechanical properties. They exhibited good thermal stability and 10% weight-loss temperatures above 540 degrees C. Their glass-transition temperatures were 263-290 degrees C. These polymers in N-methyl-2-pyrrolidinone solutions exhibited strong ultraviolet-visible absorption peaks at 307-358 nm and photoluminescence peaks around 532-590 nm in the green region. The hole-transporting and electrochromic properties were studied with electrochemical and spectroelectrochemical methods. Cyclic voltammograms of poly(amine amide) films prepared by the casting of polymer solutions onto an indium tin oxide coated glass substrate exhibited two reversible oxidation redox couples at 0.65 and 1.03 V versus Ag/AgCl in an acetonitrile solution. All the poly(amine amide)s showed excellent stability with respect to their electrochromic characteristics; the color of the films changed from pale yellow to green and then blue at 0.85 and 1.25 V, respectively. (c) 2005 Wiley Periodicals, Inc.[[note]]SC