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Article
Capturing Fleeting Intermediates in a Catalytic C-H Amination Reaction Cycle
Proceedings of the National Academy of Sciences of the United States of America
  • Richard H. Perry, Stanford University
  • Thomas J. Cahill, III, Stanford University
  • Jennifer L. Roizen, Stanford University
  • Justin Du Bois, Stanford University
  • Richard N. Zare, Stanford University
Document Type
Article
Publication Date
11-6-2012
Keywords
  • Mass spectrometry,
  • Transient intermediates,
  • C-H oxidation,
  • Catalysis
Abstract

We have applied an ambient ionization technique, desorption electrospray ionization MS, to identify transient reactive species of an archetypal C–H amination reaction catalyzed by a dirhodium tetracarboxylate complex. Using this analytical method, we have detected previously proposed short-lived reaction intermediates, including two nitrenoid complexes that differ in oxidation state. Our findings suggest that an Rh-nitrene oxidant can react with hydrocarbon substrates through a hydrogen atom abstraction pathway and raise the intriguing possibility that two catalytic C–H amination pathways may be operative in a typical bulk solution reaction. As highlighted by these results, desorption electrospray ionization MS should have broad applicability for the mechanistic study of catalytic processes.

Comments

©2012 National Academy of Sciences

Additional Comments
Air Force Office of Scientific Research grant #: FA 9550-10-1-0235; Center for Molecular Analysis and Design at Stanford University grant #: 1123893-1-AABGE; NIH fellowship #: 5F32GM089033-02
DOI
10.1073/pnas.1207600109
Citation Information
Richard H. Perry, Thomas J. Cahill, Jennifer L. Roizen, Justin Du Bois, et al.. "Capturing Fleeting Intermediates in a Catalytic C-H Amination Reaction Cycle" Proceedings of the National Academy of Sciences of the United States of America Vol. 109 Iss. 45 (2012) p. 18295 - 18299 ISSN: 0027-8424
Available at: http://works.bepress.com/richard-perry/16/