4.8 Article

Reappraising Schmidpeter's bis(iminophosphoranyl)phosphides: coordination to transition metals and bonding analysis

期刊

CHEMICAL SCIENCE
卷 12, 期 1, 页码 253-269

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0sc04736h

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资金

  1. Centre National de la Recherche Scientifique (CNRS)
  2. Universite de Bourgogne (UB)
  3. Agence Nationale de la Recherche (ALCATRAS) [ANR-16-CE07-0001-01]
  4. Conseil Regional de Bourgogne (PARI CDEA program)
  5. Conseil Regional de Bourgogne Franche-Comte
  6. Fonds Europeen de Developpement Regional (FEDER)
  7. PIA-excellence ISITE-BFC program (COMICS project)
  8. Agence Nationale de la Recherche (ANR) [ANR-16-CE07-0001] Funding Source: Agence Nationale de la Recherche (ANR)

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The synthesis and characterization of a range of bis(iminophosphoranyl)phosphide (BIPP) group 4 and coinage metals complexes is reported. Various computational tools show that the phosphorus-metal interaction is either electrostatic or dative, with the P-P bonds in both BIPP and TP being normal covalent.
The synthesis and characterization of a range of bis(iminophosphoranyl)phosphide (BIPP) group 4 and coinage metals complexes is reported. BIPP ligands bind group 4 metals in a pseudo fac-fashion, and the central phosphorus atom enables the formation of d(0)-d(10) heterobimetallic complexes. Various DFT computational tools (including AIM, ELF and NCI) show that the phosphorus-metal interaction is either electrostatic (Ti) or dative (Au, Cu). A bridged homobimetallic Cu-Cu complex was also prepared and its spectroscopic properties were investigated. The theoretical analysis of the P-P bond in BIPP complexes reveals that (i) BIPP are closely related to ambiphilic triphosphenium (TP) cations; (ii) the P-P bonds are normal covalent (i.e. not dative) in both BIPP and TP.

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