Polar Thermoplastics with Tunable Physical Properties Enabled by the Stereoregular Copolymerization of Vinyl Ethers

27 September 2019, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

A series of isotactic, semicrystalline vinyl ether copolymers (up to 94% meso diads) were synthesized using a chiral BINOL-based phosphoric acid in combination with a titanium Lewis acid. This stereoselective cationic polymerization enabled the systematic tuning of both glass-transition (Tg) and melting temperature (Tm) in copolymers derived from alkyl vinyl ethers (i.e., ethyl, butyl, isobutyl). Additionally, a vinyl ether comonomer bearing an acyl-protected alcohol was utilized as a platform for post-functionalization. Copolymers containing the masked alcohols were shown to undergo facile deprotection and subsequent coupling with a desired acid chloride. Collectively, these results highlight the diverse material properties and expanded chemical space accessible through stereoselective cationic polymerization mediated by a chiral anion.

Keywords

Stereoselective Polymerization
chiral acids
poly(vinyl ether)
polar thermoplastic
polymers

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