Bercaw, John E. and Labinger, Jay A. and Leitch, David and Steelman, Keith (2016) Homogeneous Ta/Ir tandem catalytic alkane/alkene coupling. In: 251st American Chemical Society National Meeting & Exposition, March 13-17, 2016, San Diego, CA. https://resolver.caltech.edu/CaltechAUTHORS:20160413-140044903
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Abstract
Light alkanes and alkenes are abundant but under-utilized energy carriers due to their high volatility and low energy d. A tandem catalytic approach for the coupling of alkanes and alkenes has been developed in order to upgrade these light hydrocarbons into heavier fuel mols. This process involves alkane dehydrogenation by pincer- ligated iridium complexes, and alkene dimerization by a Cp*TaCl_2(alkene) catalyst. These two homogeneous catalysts operate with up to 60 /30 cooperative turnovers (Ir/Ta) in the dimerization of 1- hexene /n- heptane, giving C_(13)/C_(14) products in 40 % yield. Because there is no kinetically relevant interaction between the two catalysts, the tandem mechanism can be entirely described using the two independent catalytic cycles. A nickel dimerization catalyst produces largely linear dimers, unlike the tantalum dimerization catalyst that produces gem- substituted dimers. Attempts to realize a truly catalytic Ni/Ir version that produces only a C_(2n) alkane from a C_n olefin and C_n alkane feed will be described.
Item Type: | Conference or Workshop Item (Paper) | ||||||
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Additional Information: | © 2016 American Chemical Society. | ||||||
Record Number: | CaltechAUTHORS:20160413-140044903 | ||||||
Persistent URL: | https://resolver.caltech.edu/CaltechAUTHORS:20160413-140044903 | ||||||
Usage Policy: | No commercial reproduction, distribution, display or performance rights in this work are provided. | ||||||
ID Code: | 66129 | ||||||
Collection: | CaltechAUTHORS | ||||||
Deposited By: | Tony Diaz | ||||||
Deposited On: | 13 Apr 2016 21:29 | ||||||
Last Modified: | 03 Oct 2019 09:53 |
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