Abstract

Novel polysiloxane derivative having adamantyl moiety in the main chain (P1) was synthesized and characterized by differential scanning calorimetry (DSC), thermogravimetry (TG), and X-ray diffraction analysis. P1 was obtained by bulk polycondensation without catalysts as well as solution polycondensation of novel disilanol monomer, i.e., 1,3-bis[4-(dimethylhydroxysilyl)phenyl]adamantane (M1), which was prepared by the Grignard reaction using chlorodimethylsilane and 1,3-bis(4-bromophenyl)adamantane, followed by the hydrolysis catalyzed by 5% palladium on charcoal. The molecular weight of P1 was dependent on the concentration of M1 in solution polycondensation, and the high concentration of M1 would result in the high average molecular weight of P1. P1 exhibited the good solubility in common organic solvents, such as tetrahydrofuran (THF), chloroform, dichloromethane, and toluene. The glass transition temperature (Tg) of P1 determined from DSC would be dependent on the average molecular weight of P1. The highest Tg was 115°C and much higher than that of poly(tetramethyl-1,4-silphenylenesiloxane) (−20°C). The melting temperature (Tm) of P1 seemed to be independent of the average molecular weight of P1 and was in the range of 153–157°C, which was comparable to the Tm of poly(tetramethyl-1,4-silphenylenesiloxane). The temperature at 5% weight loss (Td5) of P1 determined by TG was also comparable to that of poly(tetramethyl-1,4-silphenylenesiloxane), indicating that P1 is a new polysiloxane derivative with the high Tg as well as good thermostability.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.