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

      Dalton Trans.
      Royal Society of Chemistry (RSC)

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          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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          Most cited references129

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          Organophosphorus pi-conjugated materials.

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            Stoichiometric and catalytic hydroamination of alkynes and allene by zirconium bisamides Cp2Zr(NHR)2

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              Synthetic development and chemical reactivity of transition-metal silylene complexes.

              A variety of transition-metal complexes with terminal silylene ligands have become available in recent years, because of the discovery of several preparative methods. In particular, three general synthetic routes to these complexes have emerged, on the basis of anionic group abstraction, coordination of a free silylene, and alpha-hydrogen migration. The direct transformation of organosilanes to silylene ligands at a metal center (silylene extrusion) has also been observed, and this has further spurred the exploration of silylenes as ligands. This Account describes the synthetic development of silylene ligands in our laboratory and resulting investigations of stoichiometric and catalytic chemistry for these species.

                Author and article information

                Journal
                ICHBD9
                Dalton Trans.
                Dalton Trans.
                Royal Society of Chemistry (RSC)
                1477-9226
                1477-9234
                2009
                2009
                : 1
                : 18-26
                Article
                10.1039/B813332H
                19081965
                923a4d6e-68e2-4e00-8842-cee2017816be
                © 2009
                History

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