High Tg and high organosolubility of novel polyimides containing twisted structures derived from 4-(4-amino-2-chlorophenyl)-1-(4-aminophenoxy)-2,6-di-tert-butylbenzene

Abstract

A series of new polyimides (PIs) containing di-tert-butyl side groups were synthesized via the polycondensation of 4-(4-amino-2-chlorophenyl)-1-(4-aminophenoxy)-2,6-di-tert-butylbenzene ( 3) with various aromatic tetracarboxylic dianhydrides. The introduction of the asymmetric di-tert-butyl groups and twisted-biphenyl structures is an effective way to increase the inter chain distance and decrease the intermolecular interaction and packing ability of the resulted polymers. Thus, these novel PIs exhibited low dielectric constants (2.83–3.10), low moisture absorption (0.95–1.69%), excellent solubility, and high glass transition temperatures (307–456 °C). The PIs derived from the new diamine and the rigid pyromellitic dianhydride (PMDA) were soluble in N-methyl-2-pyrrolidinone, N, N-dimethylacetamide, tetrahydrofuran, m-cresol, and cyclohexanone. The polymers also show good retention of storage modulus at high temperature (325 °C). In addition, 1H NMR spectrum of the diamine 3 revealed that the protons of 4-aminophenoxy moiety are not chemical shift equivalent.