SYNTHESIS OF ORGANOMETALLIC POLYMERS
Abstract
In connection with a program to synthesize new siloxane polymers with superior resistance to attack by heat, studies were undertaken to determine the molecular structure of a thermally resistant resinous product obtained from Ph3SiOH and AlCl3, which showed a weight loss of only 9% when heated to 500 C at a rate of 180 C/hr. Efforts were also made to obtain information about the reaction mechanism. Results indicate that the material is probably a branched open-chain silicone polymer with attached cyclic siloxane trimer groups. Such materials are more thermally stable than siloxanes with only open-chain or non-cyclic branched molecular configurations. When the polymer is crosslinked through phenyl-silicon bond cleavage and transfer reactions, the thermal resistance is markedly reduced. The course of the catalytic polymer reaction involves a partial scission of the phenyl g oups bonded to the central Si atom, accompanied by a redistribution of groups, to form siloxane polymers of branched structure with attached cyclic trimer units. Exploratory studies were initiated to synthesize open-chain copolymers with SiO and M-O backbone units and branches consisting of Si-O and M-O cyclic rimer groups. Under similar catalysis conditions, Ph3SnOH is disproportionated to give (Ph2SnO)n and Ph4Sn. (Author)
Document Details
- Document Type
- Technical Report
- Publication Date
- May 08, 1962
- Accession Number
- AD0275501
Entities
People
- A.d. Delman
- A.e. Ruff
- R.j. Katzenstein