Wednesday, 16 May 2007 - 10:40 AM
Auditorium (100) (Pfahler Hall)
28

Terminal Olefins through Cobalt-Catalyzed Alkene Dimerization

Richard D. Broene1, Ethan Van Arnam1, Laura Onderko1, William M. Lamanna2, Anthony Volpe Jr3, and Maurice Brookhart3. (1) Bowdoin College, Brunswick, ME, (2) 3M Company, St. Paul, MN, (3) University of North Carolina, Chapel Hill, NC

[Cp*P(OMe)3CoCH2CH3]+ [BArF]-, generated by the addition of HBArF to Cp*P(OMe)3Co(ethene) catalyzes the oligomerization of 1-hexene to give dimers and trimers. When a deficit of the acid is used, linear &alpha olefin dimers are produced at the expense of trimeric products: e. g. 1-butene, 1-hexene, and 1-octene give 1-octene, 1-dodecene, and 1-hexadecene, respectively. The size of the phosphine ligand determines the ratio of linear to branched dimer formed in the reaction. We will discuss a novel mechanism for the reaction and the synthesis of several new complexes designed to favor linear over branched products in this reaction.


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