Published November 7, 2005
| Supplemental Material
Journal Article
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Hydrovinylation of Olefins Catalyzed by an Iridium Complex via CH Activation
Chicago
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Abstract
Olefin dimerizations are typically proposed to proceed via a Cossee−Arlman type migratory mechanism involving relatively electron-rich metal hydrides. We provide experimental evidence and theoretical calculations that show, in contrast, relatively electron-poor O-donor Ir complexes can catalyze the dimerization of olefins via a mechanism that involves olefin CH bond activation and insertion into a metal−vinyl intermediate.
Additional Information
© 2005 American Chemical Society. Received 22 July 2005. Published online 14 October 2005. Published in print 1 November 2005. The authors acknowledge Chevron Energy Technology Company, the National Science Foundation (CHE-0328121), the Loker Hydrocarbon Institute, and the University of Southern California for financial support. We acknowledge Mr. M. Yousufuddin and Prof. Robert Bau for solving the crystal structure of Vinyl−Ir−Py. The preparative procedure, spectroscopic data, elemental analysis data, and crystallographic data sets for theVinyl-Ir-Py complex as well as experimental details of the reactions discussed are available free of charge via the Internet at http//pubs.acs.org.Attached Files
Supplemental Material - om050614isi20050721_115634.cif
Supplemental Material - om050614isi20050914_100753.pdf
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Additional details
- Eprint ID
- 79352
- Resolver ID
- CaltechAUTHORS:20170725-150701014
- Chevron Energy Technology Company
- NSF
- CHE-0328121
- Loker Hydrocarbon Institute
- University of Southern California
- Created
-
2017-07-25Created from EPrint's datestamp field
- Updated
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2021-11-15Created from EPrint's last_modified field