Organo-f-element catalysts for efficient and highly selective hydroalkoxylation and hydrothiolation

Dalton Trans. 2010 Aug 7;39(29):6576-88. doi: 10.1039/c003089a. Epub 2010 May 20.

Abstract

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.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Alkynes / chemistry
  • Catalysis
  • Coordination Complexes / chemistry*
  • Lanthanoid Series Elements / chemistry*
  • Models, Molecular
  • Sulfhydryl Compounds / chemistry
  • Transition Elements / chemistry*

Substances

  • Alkynes
  • Coordination Complexes
  • Lanthanoid Series Elements
  • Sulfhydryl Compounds
  • Transition Elements