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Journal ArticleDOI

Metal-phosphido and -phosphinidene complexes in P–E bond-forming reactions

Rory Waterman
- 07 Jan 2009 - 
- Iss: 1, pp 18-26
TLDR
A selection of recent advances in metal complexes bearing terminal phosphido or phosphinidene ligands in the stoichiometric and catalytic preparation of phosphorus-element bonds are described.
Abstract
Metal complexes bearing terminal phosphido or phosphinidene ligands have become versatile tools in the stoichiometric and catalytic preparation of phosphorus–element bonds. This Perspective describes a selection of recent advances in this field, and certain emphasis has been placed on reactions that vary from what has been previously observed. Some of the general reactivity trends and mechanistic understanding in these metal-mediated reactions that has emerged are also described. Much of what is chronicled herein comes from a flux of reports over the last decade describing unique metal-mediated phosphorus–element bond formation reactions that are likely to stimulate further discoveries.

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σ-Bond Metathesis: A 30-Year Retrospective

TL;DR: A review of σ-bond metathesis is presented using Watson's 1983 observation of degenerative methyl ligand exchange at metallocene compounds as a starting point in this paper.
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Development of ruthenium catalysts for the enantioselective synthesis of P-stereogenic phosphines via nucleophilic phosphido intermediates.

TL;DR: This work details the development of ruthenium(II) catalysts for the enantioselective alkylation of chiral racemic secondary phosphines through the intermediacy of nucleophilic phosphido species, which have low barriers to pyramidal inversion.
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Mechanisms of metal-catalyzed dehydrocoupling reactions

TL;DR: A comparative approach considering dehydrocoupling reactions that appear to proceed by certain mechanistic steps is taken here, beginning with steps that are well established and general then moving to those that are newer, at least to this application.
Journal ArticleDOI

Triamidoamine-uranium(IV)-stabilized terminal parent phosphide and phosphinidene complexes

TL;DR: DFT calculations reveal a polarized-covalent UP bond with a Mayer bond order of 1.92 and the unprecedented metal-stabilized terminal parent phosphinidene complex.
Journal ArticleDOI

Metal complexes of planar PR2 ligands: Examining the carbene analogy

TL;DR: In this article, the authors classify planar M-PR2 complexes in the same way as planar CR2 complexes, based on their structures, reactivities, and/or syntheses.
References
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