Departament de Química, Universitat Autònoma de Barcelona, 08193 Cerdanyola del Vallès, Spain.
Beilstein J Org Chem. 2013 Jul 9;9:1352-82. doi: 10.3762/bjoc.9.153. eCollection 2013.
Although four-coordinate square-planar geometries, with a formally 16-electron counting, are absolutely dominant in isolated Pt(II) complexes, three-coordinate, 14-electron Pt(II) complexes are believed to be key intermediates in a number of platinum-mediated organometallic transformations. Although very few authenticated three-coordinate Pt(II) complexes have been characterized, a much larger number of complexes can be described as operationally three-coordinate in a kinetic sense. In these compounds, which we have called masked T-shaped complexes, the fourth position is occupied by a very weak ligand (agostic bond, solvent molecule or counteranion), which can be easily displaced. This review summarizes the structural features of the true and masked T-shaped Pt(II) complexes reported so far and describes synthetic strategies employed for their formation. Moreover, recent experimental and theoretical reports are analyzed, which suggest the involvement of such intermediates in reaction mechanisms, particularly C-H bond-activation processes.
虽然具有四配位平面正方形几何形状、形式上具有 16 个电子计数的 Pt(II) 配合物是绝对占主导地位的,但三配位、14 个电子的 Pt(II) 配合物被认为是许多铂介导的有机金属转化中的关键中间体。尽管已经证实的三配位 Pt(II) 配合物很少,但在动力学意义上可以描述更多的配合物为操作上的三配位。在这些化合物中,我们称之为掩蔽的 T 形配合物,第四个位置被一个非常弱的配体(螯合键、溶剂分子或抗衡阴离子)占据,它很容易被取代。这篇综述总结了迄今为止报道的真实和掩蔽的 T 形 Pt(II) 配合物的结构特征,并描述了用于它们形成的合成策略。此外,还分析了最近的实验和理论报告,这些报告表明这些中间体参与了反应机制,特别是 C-H 键活化过程。