Laboratorio de Catálisis Homogénea, Departamento de Química y Ciencias de los Materiales, Unidad Asociada al CSIC, Centro de Investigación en Química Sostenible (CIQSO), Universidad de Huelva, Campus de El Carmen s/n, 21007 Huelva, Spain.
Dalton Trans. 2013 Mar 28;42(12):4132-8. doi: 10.1039/c2dt32439c.
We examined the ability of Tp(x)M (Tp(x) = hydrotris(pyrazolyl)borate ligand; M = Cu and Ag) and IPrMCl (IPr = 1,3-bis(diisopropylphenyl)imidazol-2-ylidene; M = Cu, Ag, Au) complexes as catalyst precursors for the cross-coupling of diazo compounds. Experimental data showed that the metal centre can be tuned with the appropriate selection of the ligand to yield either the homo- or hetero-coupling (cross-coupling) products. A computational study of the reaction mechanism allowed the rationalization of the experimental reactivity patterns, and the identification of the key reaction step controlling the selectivity: the initial reaction between the metallocarbene intermediate and one of the diazo compounds.
我们考察了 Tp(x)M(Tp(x) = 氢三(吡唑基)硼酸盐配体;M = Cu 和 Ag)和 IPrMCl(IPr = 1,3-双(二异丙基苯基)咪唑-2-亚基;M = Cu、Ag、Au)配合物作为重氮化合物交叉偶联的催化剂前体的能力。实验数据表明,通过适当选择配体,可以调整金属中心,从而得到同偶联(交叉偶联)产物或异偶联产物。对反应机理的计算研究允许对实验反应性模式进行合理化,并确定控制选择性的关键反应步骤:金属卡宾中间体与重氮化合物之一的初始反应。