Department of Chemistry, Northwestern University, Evanston, Illinois 60208, USA.
Dalton Trans. 2010 Aug 7;39(29):6576-88. doi: 10.1039/c003089a. Epub 2010 May 20.
Lanthanide and actinide catalysts have made significant contributions to many areas of homogeneous catalysis with hydroelementation of C-C unsaturation being a notable area of success. In this Perspective, we review recent advances in f-element hydroelementation for highly selective hydroalkoxylation and hydrothiolation processes. As will be discussed, f-element hydroalkoxylation and hydrothiolation catalysts exhibit selectivities unobtainable by many late transition metal complexes. First, we review lanthanide-mediated hydroalkoxylation processes with mechanistic, thermodynamic, and kinetic considerations discussed, and then compare/contrast them with analogous C-N and C-P bond-forming transformations. In addition, computational studies are discussed which provide further insight into this transformation and the observed selectivities. Next, actinide-mediated alkyne hydrothiolation is reviewed with a similar discussion of reactivity, mechanism, and thermodynamics.
镧系和锕系元素催化剂在均相催化的许多领域做出了重大贡献,其中 C-C 不饱和加氢是一个显著的成功领域。在本观点中,我们综述了近年来 f 族元素在高选择性氢烷氧基化和氢硫醚化反应中的应用进展。正如将讨论的那样,f 族元素氢烷氧基化和氢硫醚化催化剂表现出许多后过渡金属配合物无法获得的选择性。首先,我们综述了镧系元素介导的氢烷氧基化过程,并讨论了其反应机理、热力学和动力学方面的考虑因素,然后将其与类似的 C-N 和 C-P 键形成转化进行了比较/对比。此外,还讨论了计算研究,这些研究为这一转化和观察到的选择性提供了进一步的见解。接下来,综述了锕系元素介导的炔烃氢硫醚化反应,讨论了其反应性、机理和热力学。