ABSTRACT
A series of polyesterimides based on aromatic bis(trimellitate) dian-hydride in main chain were prepared by polycondensation of t-butyl-p-phenylenebis(trimellitate) dianhydride (BPBDA) and phenylene bis(trimellitate) dianhydride (PBDA) with benzidine and its derivates. The results show that the incorporation of noncoplanar structure led by introducing alkyl substituents on dianhydride and benzidine can improve the solubility of polyesterimides in organic solvents. It also displays that the introducing substituents lead to a decrease in glass transition temperature and influence the β relaxation of PEsI. By comparing the chemical structure and the dynamical mechanic date, we suggest that the β relaxation correspond to the motion involving the imide ring and phenylene groups of the diamine.
ACKNOWLEDGMENT
This work project 50043011 was supported by the National Science Foundation of China.