Photocatalytic C–H activation and the subtle role of chlorine radical complexation in reactivity

Author:

Yang Qiaomu1ORCID,Wang Yu-Heng1ORCID,Qiao Yusen1ORCID,Gau Michael1ORCID,Carroll Patrick J.1,Walsh Patrick J.1ORCID,Schelter Eric J.1ORCID

Affiliation:

1. P. Roy and Diana T. Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, 231 South 34th Street, Philadelphia, PA 19104, USA.

Abstract

A complex role for chlorine radicals Radicals are atoms or molecules that are highly reactive because they have an unpaired electron. A common means of investigating whether they are involved in a particular reaction is to try to trap them with an acceptor compound. Yang et al. reinvestigated a photoinduced alkane oxidation reaction for which a trapping study had previously implicated alkoxy radicals. Their spectroscopic, kinetic, and isotopic labeling studies revealed that chlorine, rather than alkoxy, was the key radical intermediate; the prior trapping results had stemmed from its complexation with alcohols. Science , abd8408, this issue p. 847

Funder

National Science Foundation

Basic Energy Sciences

Vagelos Institute for Energy Science and Technology

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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