Design and synthesis of low‐dieclectric polyaryl ethers containing bulky tetraphenyl vinyl pendant group

Abstract A tetraphenylethylene‐containing bisphenol monomer 5‐[4‐(triphenylvinyl)phenyl]benzene‐1,3‐diol (TPE‐OH) was designed and synthesized by Suzuki coupling and nucleophilic substitution reaction. By adjusting the proportion of TPE‐OH, a series of rigid polyaryl ether, namely PPTES, were facilely synthesized by homopolymerization or copolymerization with 4‐(4‐hydroxyphenyl)‐2,3‐diazepine‐1‐one (DHPZ) and 4,4′‐difluorodiphenyl sulfone (DFS). The following characterization of their structures with nuclear magnetic resonance and infrared spectroscopy confirmed successful synthesis of both monomers and polymers. Large, volume‐twisted and non‐coplanar rigid tetraphenylethylene could effectively increase the molecular chain spacing and reduce the regularity of the molecular chain, as evidenced by molecular dynamics simulation with Materials Studio, in turn to form an amorphous nature of PPTES phase state. In addition, such PPTESs have excellent solubility, heat resistance, and other comprehensive properties. Their glass transition temperature ( T g ) is between 219 and 300°C, and the 5% thermogravimetric temperature of PPTESs locates at 490–539°C under N 2 atmosphere. At 1 GHz, the intrinsic dielectric permittivity of polymer films is between 2.32 and 2.61, gradually decreases with TPE‐OH content. This work would provide new idea and choice for the selection of polyaryl ether resin bisphenol monomer, and promote the development and application of low‐dielectric polyarylether materials.