Direct Evidence for the Sulfonium-Mediated Photopolymerization of 1,2-Dithiolanes

Light-induced, initiatorless homopolymerization of 1,2-dithiolanes is widely attributed to radical propagation. However, several experimental observations, including copolymerization behavior and EPR measurements, are inconsistent with this assignment. Here, this reaction is examined using in situ photoNMR, revealing first-order monomer consumption that is incompatible with a propagating radical mechanism. PhotoNMR further enables direct observation of a sulfonium intermediate attributed to a charge-transfer complex, corroborated through steady-state and transient absorption spectroscopy. Together, these data establish an activated-monomer-type polymerization, proceeding through a cationic rather than radical pathway. This same intermediate also enables controlled chain growth and is leveraged as a photoinitiator for cationic vinyl ether polymerization, extending the scope of dithiolane photochemistry beyond homopolymer formation and opening new opportunities for dithiolane-based photopolymerization strategies.

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Journal
Journal of the American Chemical Society
Published
2026-06-27
DOI
https://doi.org/10.1021/jacs.6c08542
Primary Topic
Photopolymerization techniques and applications
Type
article
Field-Weighted Citation Impact
0.00

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article

Direct Evidence for the Sulfonium-Mediated Photopolymerization of 1,2-Dithiolanes

Niels H. Damrauer, Christopher N. Bowman, Benjamin R. Nelson, Taime R. Clark et al.
Journal of the American Chemical Society
Photopolymerization techniques and applications
article

Direct Evidence for the Sulfonium-Mediated Photopolymerization of 1,2-Dithiolanes

Niels H. Damrauer, Christopher N. Bowman, Benjamin R. Nelson, Taime R. Clark, John F. Rynk, Keith J. Fritzsching, Emeline C. Lochmaier, Benjamin D. Fairbanks, Kristi S. Anseth, Bruce E. Kirkpatrick, Leah N. Appelhans
article en

Abstract

Light-induced, initiatorless homopolymerization of 1,2-dithiolanes is widely attributed to radical propagation. However, several experimental observations, including copolymerization behavior and EPR measurements, are inconsistent with this assignment. Here, this reaction is examined using in situ photoNMR, revealing first-order monomer consumption that is incompatible with a propagating radical mechanism. PhotoNMR further enables direct observation of a sulfonium intermediate attributed to a charge-transfer complex, corroborated through steady-state and transient absorption spectroscopy. Together, these data establish an activated-monomer-type polymerization, proceeding through a cationic rather than radical pathway. This same intermediate also enables controlled chain growth and is leveraged as a photoinitiator for cationic vinyl ether polymerization, extending the scope of dithiolane photochemistry beyond homopolymer formation and opening new opportunities for dithiolane-based photopolymerization strategies.

Journal of the American Chemical Society
Energy Institute (GB), University of Colorado Boulder (US), University of Colorado System (US), Infrafrontier (DE), Sandia National Laboratories (US), Division of Materials Science and Engineering (AU), National Student Clearinghouse Research Center (US), University of Colorado Anschutz Medical Campus (US)
National Heart, Lung, and Blood Institute, Workforce Development for Teachers and Scientists
Openalex Percentile: Top 12%
Photopolymerization techniques and applications
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