UCR-CNRS Joint Research Chemistry Laboratory (UMI 2957), Department of Chemistry, University of California, Riverside, CA 92521-0403, USA.
Angew Chem Int Ed Engl. 2010 Jun 28;49(28):4759-62. doi: 10.1002/anie.201001864.
Until recently, the availability of neutral carbon-based κC ligands was limited to carbon monoxide, isocyanides, and carbenes. Compared to phosphorus-based ligands, carbenes tend to bind more strongly to metal centers, avoiding the necessity for the use of excess ligand in catalytic reactions. The corresponding complexes are often less sensitive to air and moisture, and are remarkably resistant to oxidation. As the robustness of carbene complexes is largely due to the presence of strong carbon–metal bonds, other types of carbon-based ligands are highly desirable. It is noteworthy that, although complexes between a carbene and a transition metal have been known for a long time, the recent developments in their application in catalysis have been greatly facilitated by the availability of carbenes that are stable enough to be bottled. Moreover, carbenes, especially imidazol-2-ylidenes and 1,2,4-triazol-5-ylidenes , are also excellent organocatalysts (Scheme 1).
直到最近,中性碳基 κC 配体的可用性还仅限于一氧化碳、异氰化物和卡宾。与磷基配体相比,卡宾往往与金属中心结合得更牢固,从而避免了在催化反应中使用过量配体的必要性。相应的配合物通常对空气和水分的敏感性较低,并且对氧化具有显著的抵抗力。由于卡宾配合物的稳健性在很大程度上归因于存在强的碳-金属键,因此非常需要其他类型的碳基配体。值得注意的是,尽管卡宾与过渡金属之间的配合物已经存在了很长时间,但由于能够稳定地装瓶的卡宾的可用性,它们在催化中的应用最近得到了极大的促进。此外,卡宾,特别是咪唑-2-亚基和 1,2,4-三唑-5-亚基,也是出色的有机催化剂(方案 1)。