Influence of the Alkene Structure On the Mechanism and Kinetics of Thiol-Alkene Photopolymerizations With Real-Time Infrared Spectroscopy

Document Type

Article

Publication Date

12-15-2004

Department

Polymers and High Performance Materials

Abstract

The effect of the chemical structure on the reactivity of alkenes used in thiol-ene photopolymerizations has been investigated with real-time infrared spectroscopy. Model studies of thiol-ene photoreactions with various monofunctional hydrocarbon alkenes and the monofunctional thiol ethyl-3-mercaptopropionate have been performed to identify and understand structure-reactivity relationships. The results demonstrate that terminal enes react very rapidly with thiol, achieve complete conversion, and are independent of the aliphatic hydrocarbon substituent length. Disubstitution on a single carbon of a terminal ene significantly reduces the reactivity, whereas substitution on the carbon a to the terminal ene has a minimal influence on the reactivity. Internal trans enes display reduced reactivity and a lower overall conversion and deviate from the standard thiol-ene reaction mechanism because of steric strain induced by 1,3-interactions. The reactivity and conversion of internal trans enes decrease as the substituents on the ene become larger, reaching a minimum when the substituent size is greater than or equal to that of propyl groups. Internal cis enes react rapidly with thiol; however, they undergo a fast isomerization-elimination reaction sequence generating the trans ene, which proceeds to react at a reduced rate with thiol. The reactivity of cyclic enes is dictated by ring strain, stereoelectronic effects, and hydrogen abstractability. The reactivity trends in the model studies have been used to explain the photopolymerization mechanism and kinetics of a series of multifunctional thiol-ene systems. (C) 2004 Wiley Periodicals, Inc.

Publication Title

Journal of Polymer Science Part A-Polymer Chemistry

Volume

42

Issue

24

First Page

6283

Last Page

6298

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