## Abstract Polyhedral oligomeric silsesquioxane (POSS) polymers were synthesized by the dehydrogenative condensation of (HSiO~3/2~)~8~ with water in the presence of diethylhydroxylamine followed by trimethylsilylation. Coating films were prepared by spin‐coating of the coating solution prepared by
Preparation and properties of polyhedral oligomeric silsesquioxane–polysiloxane copolymers
✍ Scribed by Takahiro Gunji; Takahiro Shioda; Koji Tsuchihira; Hiroyasu Seki; Takashi Kajiwara; Yoshimoto Abe
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 158 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0268-2605
- DOI
- 10.1002/aoc.1562
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✦ Synopsis
Abstract
All siloxane‐type siloxane–polyhedral oligomeric silsesquioxane [(HSiO~3/2~)~8~, T~8~^H^] copolymers were synthesized by the dehydrogenative condensation of T~8~^H^ with diphenylsilanediol, tetraphenyldisiloxane‐1,3‐diol or silanol‐terminated polydimethylsiloxanes in the presence of diethylhydroxylamine followed by trimethylsilylation. Coating films were prepared by spin‐coating of the coating solutions prepared from the dehydrogenative condensation products. The hardness of the coating films was evaluated by a pencil hardness test and was found to increase up to 6H with increases in the curing temperature. Silica gels were prepared by concentrating the coating solution following by pyrolysis. These silica gels showed a specific surface area 449 m^2^/g at 650 °C corresponding to the formation of a silica network in response to combustion of the phenyl groups. Copyright © 2009 John Wiley & Sons, Ltd.
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We report on the viscoelastic behavior of linear thermoplastic nonpolar hybrid inorganic-organic polymers. These materials have been synthesized through copolymerization of an oligomeric inorganic macromer with 4-methylstyrene where the inorganic portion of the material is a well-defined polyhedral