Laboratory for Organic Chemistry, ETH Zürich, Wolfgang-Pauli-Strasse 10, 8093 Zürich, Switzerland.
Angew Chem Int Ed Engl. 2012 Jul 16;51(29):7226-30. doi: 10.1002/anie.201202504. Epub 2012 Jun 11.
Challenging a catalytic cycle: Pd(0) catalysts are readily oxidized by Cu and Ag salts to give dinuclear Pd(I) complexes and Cu(I) or Ag(I) cubanes (see scheme). The reactivities of the resulting Pd(I) dimers are consistent with several observations of additive effects in cross-coupling chemistry. The results indicate the possibility for alternative catalytic cycles involving dinuclear Pd(I) complexes over the currently accepted synergistic cycles involving Pd(0)/Pd(II) intermediates and Cu or Ag.
Pd(0)催化剂很容易被 Cu 和 Ag 盐氧化,生成双核 Pd(I)配合物和 Cu(I)或 Ag(I)立方烷(见方案)。所得 Pd(I)二聚体的反应活性与交叉偶联化学中加性效应的几个观察结果一致。这些结果表明,可能存在替代的催化循环,涉及双核 Pd(I)配合物,而不是目前公认的涉及 Pd(0)/Pd(II)中间体和 Cu 或 Ag 的协同循环。