Products Cited in Publications Worldwide Tuning Porosity in Triptycene-Poly(arylene ether)s

Tuning Porosity in Triptycene-Poly(arylene ether)s

Kayla R. Storme; Benedikt S. Schreib; Zachary P. Smith; Timothy M. Swager

DOI:

Abstract

We report a scalable synthesis of high-molecular-weight poly(arylene ether)s (PAEs) using decafluorobiphenyl under SNAr reaction conditions and the preparation of enantiopure (R,R)-6,11-di(tert-butyl)triptycene-1,4-hydroquinone. The nonfluorinated biphenyl-based PAE was also synthesized using Pd-catalyzed C–O coupling methods, and structure–property comparisons were made from the different biphenyl-based polymers. The integration of free-volume-promoting triptycene moieties on the main chain gives rise to intrinsic porosity, which can be further modulated by incorporating biphenyl or perfluorobiphenyl comonomers. The nonfluorinated PAE exhibited a BET surface area of 270 m2 g–1, whereas the racemic and enantiopure fluorinated PAEs showed higher BET surface areas of 454 and 368 m2 g–1, respectively. WAXS analysis revealed that all of the polymers tested have a greater disruption of chain packing compared to related polyimides, with the fluorinated PAEs having the highest average interchain spacing. The fluorinated PAEs also demonstrated high gas permeability as a result of their free volume. The triptycene-based PAEs also were resistant to plasticization even at CO2 pressures of ∼31 bar.

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