Hyperbranched Poly(phenylenesilolene)s: Synthesis, Thermal Stability, Electronic Conjugation, Optical Power Limiting, and Cooling-Enhanced Light Emission

Abstract

Silole-containing hyperbranched polyphenylenes ( 1 ) are synthesized, which exhibit high thermal stability, extended electronic conjugation, excellent optical power limiting performance, and novel cooling-enhanced photoluminescence. The homopolycyclotrimerization of 1,1-diethynyl-2,3,4,5-tetraphenylsilole ( 2 ) and its copolycyclotrimerizations with 1-octyne catalyzed by TaCl 5 −Ph 4 Sn proceed smoothly at room temperature and produce completely soluble polymers in high yields (up to ∼85%). The molecular structures of 1 are characterized by spectroscopic analyses. The thermal stability of 1 is evaluated by thermogravimetric analyses, which detect virtually no weight losses when the polymers are heated to ∼300 °C. The hyperbranched polyphenylenes are electronically conjugated, as suggested by their strong absorption in the visible spectral region ( λ max ∼ 520 nm). Because of this extended electronic conjugation, polymers 1 are nonlinear optically active and strongly attenuate the optical power of intense laser pulses, whose optical limiting performances are superior to that of C 60, the best-known optical limiter. The photoluminescence of the polymers is dramatically enhanced by cooling their solutions to low temperatures. This unique phenomenon of cooling-enhanced emission is probably caused by the restricted intramolecular rotations of the phenyl rings upon the axes of the single bonds linked to the silole cores at the cryogenic temperatures.