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Published January 1, 2018 | Supplemental Material
Journal Article Open

Triphenylsulfonium topophotochemistry

Abstract

The products from the 193 nm irradiation of triphenylsulfonium nonaflate (TPS) embedded in a poly(methyl methacrylate) (PMMA) film have been characterized. The analysis of the photoproduct formation was performed using chromatographic techniques including HPLC, GPC and GC-MS as well as UV-vis and NMR spectroscopic methods. Two previously unreported TPS photoproducts, triphenylene and dibenzothiophene, were detected; additionally, GPC and DOSY-NMR spectroscopic analyses after irradiation suggested that TPS fragments had been incorporated into the polymer film. The irradiation of acetonitrile solutions containing 10% w/v PMMA and 1% w/v TPS in a 1 cm-path-length cuvette showed only a trace amount of triphenylene or dibenzothiophene, indicating that topochemical factors were important for the formation of these molecules. The accumulated evidence indicates that both products were formed by in-cage, secondary photochemical reactions: 2-(phenylthio)biphenyl to triphenylene, and diphenylsulfide to dibenzothiophene.

Additional Information

© 2017 The Royal Society of Chemistry and Owner Societies. The article was received on 25 Aug 2017, accepted on 03 Nov 2017 and first published on 03 Nov 2017. We thank Dr VanderVelde for his help on the DOSY-NMR experiment. This work was supported by the National Science Foundation Center for Chemical Innovation in Solar Fuels (CHE-1305124) and in part by The Dow Chemical Company through a university partnership program (Agreement # 227027AK). There are no conflicts to declare.

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August 19, 2023
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