Issue 15, 2012

PCP-bridged chalcogen-centred anions: coordination chemistry and carbon-based reactivity

Abstract

Since the discovery of the stabilising influence of thiophosphinoyl groups in methanediides by Le Floch et al. (Angew. Chem. Int. Ed., 2004, 43, 6382), numerous transition metal, lanthanide and actinide complexes of bis(thiophosphinoyl) carbene ligands have been investigated with an emphasis on the electronic structure and reactivity of the metal–carbon bonds. This Perspective begins by discussing main group (s- and p-block) complexes of this ligand and draws attention to differences compared to their d and f-block analogues. Investigations targeting the heavy chalcogen analogues of the Le Floch ligand have revealed an unusual carbon-based reactivity that led to the discovery of novel multidentate chalcogen-centred ligands as both monomers and, upon oxidation, dimers linked by dichalcogenido functionalities. Studies of main group and coinage metal complexes have established the flexibility and redox-activity of these novel anionic ligands.

Graphical abstract: PCP-bridged chalcogen-centred anions: coordination chemistry and carbon-based reactivity

Article information

Article type
Perspective
Submitted
06 gruod. 2011
Accepted
18 saus. 2012
First published
06 kov. 2012

Dalton Trans., 2012,41, 4283-4295

PCP-bridged chalcogen-centred anions: coordination chemistry and carbon-based reactivity

T. Chivers, J. Konu and R. Thirumoorthi, Dalton Trans., 2012, 41, 4283 DOI: 10.1039/C2DT12361D

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements