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Correlation between structural and solution calorimetric data for Cp*Ru(PR3)(2)Cl (Cp* = C5Me5) complexes

  • D C Smith
  • , C M Haar
  • , L B Luo
  • , C B Li
  • , M E Cucullu
  • , C H Mahler
  • , Steven Patrick Nolan
  • , W J Marshall
  • , N L Jones
  • , P J Fagan

Research output: Contribution to journalArticlepeer-review

Abstract

Single-crystal X-ray diffraction studies were conducted bn the following compounds: Cp*Ru(PMe3)(2)Cl (1), Cp*Ru(PPhMe2)(2)Cl (2), Cp*Ru(PMePh2)(2)Cl (3), Cp*Ru(PPh3)(2)Cl (4), Cp*Ru(PEt3)(2)Cl (5), Cp*Ru(AsEt3)(2)Cl (6), Cp*Ru((PBu3)-Bu-n)(2)Cl (7), and Cp*Ru(dmpm)Cl (8). Structural information obtained from these X-ray studies can be correlated with enthalpies of ligand substitution previously determined from solution calorimetry. The cone angle of the phosphine ligand (monodentate) and the Ru-P bond distance were found to be proportional to the enthalpy of reaction.

Original languageEnglish
Pages (from-to)2357-2361
Number of pages5
JournalOrganometallics
Volume18
Issue number12
DOIs
Publication statusPublished - 7 Jun 1999

Keywords

  • TERTIARY PHOSPHINE-LIGANDS
  • ORGANORUTHENIUM THERMOCHEMISTRY
  • PHOSPHORUS LIGANDS
  • ENTHALPIES
  • SUBSTITUTION
  • ENERGIES
  • SYSTEM
  • MONODENTATE
  • CHEMISTRY
  • FRAGMENT

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