Mechanism of Side Reactions in Alkane C-H Bond Functionalization by Diazo Compounds Catalyzed by Ag and Cu Homoscorpionate Complexes-A DFT Study

作者：Braga Ataualpa A C; Caballero Ana; Urbano Juan; Mar Diaz Requejo M; Perez Pedro J^*; Maseras Feliu

来源：ChemCatChem, 2011, 3(10): 1646-1652.

DOI：10.1002/cctc.201100082

• carbene ligands
• C-H activation
• density functional calculations
• diazo compounds
• homoscorpionate ligands

DFT computational methods were applied to the mechanistic study of the formation of fumarate and maleate derivatives in a solution containing alkane, Tp(Br3)M [M = Cu, Ag; Tp(Br3) = hydrotris(3,4,5-tribromopyrazolyl)borate] and methyl diazoacetate. These solutions are the experimentally reported conditions for carbene insertion into alkane C-H bonds, a procedure that usually competes with a nondesired reaction, producing fumarate and/or maleate derivatives. Several mechanisms are analyzed. The preferred mechanism proceeds through a direct reaction between a metallocarbene complex intermediate and a diazo molecule. The computational results explain all of the available experimental evidence and provide important information on the behavior of these systems.

• 出版日期2011-10