Peruzzini Maurizio, Gonsalvi Luca, Romerosa Antonio
Istituto di Chimica dei Composti Organometallici ICCOM-CNR, Via Madonna del Piano 10, 50019 Sesto Fiorentino, Firenze, Italy.
Chem Soc Rev. 2005 Dec;34(12):1038-47. doi: 10.1039/b510917e. Epub 2005 Oct 13.
The chemistry of phosphorus is nowadays rivaling that of carbon in terms of complexity and diversity. This tutorial review highlights the state-of-the-art in the field of metal-mediated activation and functionalization of white phosphorus. Particular attention is given to an illustration of the coordination abilities of the intact molecule as well as the disaggregating and reaggregating metal-mediated processes resulting in different polyphosphorus ligands from P(1) to P(12). The metal-promoted P-C and P-H bond forming processes are also reviewed showing that an ecoefficient catalytic protocol for transforming P(4) into high value organophosphorus compounds is a concrete possibility for chemical companies. This tutorial review deals with the activation and functionalization of white phosphorus in the coordination sphere of transition metal complexes. Particular attention is given to the coordination abilities of the intact molecule as well as to the disaggregating and reaggregating metal-mediated processes yielding various polyphosphorus ligands from P(1) to P(12). The metal-promoted processes for P-C and P-H bond formation are also reviewed showing that an ecoefficient catalytic protocol for transforming P(4) into high value organophosphorus compounds offers good opportunities for chemical companies.
如今,磷的化学在复杂性和多样性方面可与碳的化学相媲美。本专题综述重点介绍了白磷金属介导的活化和功能化领域的最新进展。特别关注完整分子的配位能力以及金属介导的分解和重新聚集过程,这些过程会产生从P(1)到P(12)的不同多磷配体。还综述了金属促进的P-C和P-H键形成过程,表明将P(4)转化为高价值有机磷化合物的生态高效催化方案对化工公司来说是切实可行的。本专题综述涉及过渡金属配合物配位领域中白磷的活化和功能化。特别关注完整分子的配位能力以及产生从P(1)到P(12)的各种多磷配体的金属介导的分解和重新聚集过程。还综述了金属促进的P-C和P-H键形成过程,表明将P(4)转化为高价值有机磷化合物的生态高效催化方案为化工公司提供了良好机遇。