Sulfur-Containing Silsesquioxane Derivatives Obtained by the Thiol-ene Reaction: Synthesis and Thermal Degradation

Abstract

This article presents the synthesis of new derivatives of octa(3-thiopropyl)silsesquioxane (SSQ-8SH) via thiol-ene reaction with simple olefins bearing alkyl groups as well as methoxysilyl, substituted aryl or fluoroalkyl groups. All products were characterized by ¹ H NMR, ¹³ C NMR, ²⁹ Si NMR, FTIR, GPC, MALDI-TOF-MS, as well as thermal analysis (TGA) to confirm their structures, purity and thermal stability, and finally give some insight into their thermal degradation pathway. In some of the structures obtained, the T_5% values take place at high temperatures and are close to 230 °C. The thiol-ene reaction allowed to obtain 7 new compounds with high yield (>92 %), no by-products and in a relatively short time (24 h). All products are characterized by high conversion >99 %. New derivatives can find potential use as modifiers of plastics to improve their certain properties for example hydrophobicity or thermo-oxidative stability.

Keywords: cage compounds; silsesquioxanes; sulfur; thermal degradation; thiol-ene reaction.