An Efficient Synthesis of Geminal-Dialkyl Dienes for Olefin Metathesis Polymerization.

Macromolecules

The Arnold and Mabel Beckman Laboratory of Chemical Synthesis, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, United States.

Published: September 2020

A robust synthesis of -dialkyl acyclic diene monomers has been developed. This route is scalable, flexible, and biorenewable, allowing for the production of a wide range of diene monomers of different lengths and different -dialkyl substitution starting from unsaturated esters derived from seed oils. The metathesis polymerization of these monomers and the hydrogenation of the resulting polyolefins leads to telechelic -dialkyl polyethylenes, which can be used as elastomers in the synthesis of polyurethanes and other block polymers.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8297823PMC
http://dx.doi.org/10.1021/acs.macromol.0c01606DOI Listing

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