Sarazin Yann, Carpentier Jean-François
Organometallics: Materials and Catalysis, Institut des Sciences Chimiques de Rennes UMR 6226 CNRS - Université de Rennes 1, Campus de Beaulieu, 35042, Rennes Cedex, France.
Chem Rec. 2016 Dec;16(6):2482-2505. doi: 10.1002/tcr.201600067. Epub 2016 Jun 29.
The large alkaline earths (Ae), calcium, strontium and barium, have in the past 15 years yielded a brand new generation of heteroleptic molecular catalysts for the production of fine chemicals. However, the integrity of these complexes is often plagued by ligand redistribution equilibria in solution. This personal account retraces the paths followed in our research group towards the design of stable heteroleptic alkalino-earth complexes, including the use of intramolecular noncovalent Ae···H-Si and Ae···F-C interactions. Their implementation as homogenous precatalysts for reactions such as the intramolecular and intermolecular hydroamination and hydrophosphination of activated alkenes, the hydrophosphonylation of ketones, and the dehydrogenative coupling of amines and hydrosilanes that enable the efficient and controlled formations of CP, CN, or SiN σ-bonds, is presented in a synthetic perspective that highlights their overall outstanding catalytic performance.
大型碱土金属(Ae),即钙、锶和钡,在过去15年中产生了用于精细化学品生产的全新一代杂配分子催化剂。然而,这些配合物的完整性常常受到溶液中配体再分布平衡的困扰。本个人综述追溯了我们研究小组在设计稳定的杂配碱土配合物方面所走的道路,包括使用分子内非共价Ae···H-Si和Ae···F-C相互作用。从合成角度介绍了它们作为均相预催化剂用于诸如活化烯烃的分子内和分子间氢胺化和氢膦化、酮的氢膦酰化以及胺与氢硅烷的脱氢偶联等反应,这些反应能够高效且可控地形成CP、CN或SiN σ键,突出了它们总体出色的催化性能。