| Literature DB >> 17183598 |
Vanesa Lillo1, Manuel R Fructos, Jesús Ramírez, Ataualpa A C Braga, Feliu Maseras, M Mar Díaz-Requejo, Pedro J Pérez, Elena Fernández.
Abstract
The complexes [Cu(NHC)(NCMe)]BF4 (NHC=N-heterocyclic ligand), with bis(catecholato)diboron (B2(cat)2) as the boron source, efficiently catalyze the diboration of styrene with very high degrees of conversion. With the appropriate NHC ligand, the reaction proceeds quantitatively toward the diborated derivative PhCH(Bcat)--CH2(Bcat). The [styrene]/[B2(cat)2] ratio also has a strong effect on the selectivity: the use of an excess of styrene allows modification of the selectivity toward the formation solely of the monoborated derivative, PhCH2--CH2(Bcat). DFT calculations suggest that no oxidative addition processes take place at copper, but that intermediates containing coordinated sigma-bonds are involved in the catalytic cycle.Entities:
Year: 2007 PMID: 17183598 DOI: 10.1002/chem.200601146
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236