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Highly Electrophilic Titania Hole as a Versatile and Efficient Photochemical Free Radical Source

Hainer, Andrew; Marina, Nancy; Rincon, Stefanie; Costa, Paolo; Lanterna, Anabel E.; Scaiano, Juan C.

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Authors

Andrew Hainer

Nancy Marina

Stefanie Rincon

Paolo Costa

Juan C. Scaiano



Abstract

Photogenerated holes in nanometric semiconductors, such as TiO2, constitute remarkable powerful electrophilic centers, capable of capturing an electron from numerous donors such as ethers, or nonactivated substrates like toluene or acetonitrile, and constitute an exceptionally clean and efficient source of free radicals. In contrast with typical free radical precursors, semiconductors generate single radicals (rather than pairs), where the precursors can be readily removed by filtration or centrifugation after use, thus making it a convenient tool in organic chemistry. The process can be described as an example of dystonic proton coupled electron transfer.

Citation

Hainer, A., Marina, N., Rincon, S., Costa, P., Lanterna, A. E., & Scaiano, J. C. (2019). Highly Electrophilic Titania Hole as a Versatile and Efficient Photochemical Free Radical Source. Journal of the American Chemical Society, 141(11), 4531-4535. https://doi.org/10.1021/jacs.8b13422

Journal Article Type Article
Acceptance Date Mar 4, 2019
Online Publication Date Mar 4, 2019
Publication Date Mar 20, 2019
Deposit Date Jun 22, 2020
Publicly Available Date Aug 7, 2020
Journal Journal of the American Chemical Society
Print ISSN 0002-7863
Electronic ISSN 1520-5126
Publisher American Chemical Society
Peer Reviewed Peer Reviewed
Volume 141
Issue 11
Pages 4531-4535
DOI https://doi.org/10.1021/jacs.8b13422
Keywords Colloid and Surface Chemistry; Biochemistry; General Chemistry; Catalysis
Public URL https://nottingham-repository.worktribe.com/output/4442864
Publisher URL https://pubs.acs.org/doi/10.1021/jacs.8b13422
Additional Information This document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of the American Chemical Society, copyright © 2019 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://pubs.acs.org/doi/10.1021/jacs.8b13422

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