6533b853fe1ef96bd12acc8a

RESEARCH PRODUCT

First donor stabilized-phosphenium rhodium complexes

Michèle AzouriPhilippe RichardJacques Andrieu

subject

Halidechemistry.chemical_elementCrystal structure010402 general chemistryPhotochemistry01 natural sciencesAdductRhodiumInorganic Chemistrychemistry.chemical_compounddonor–acceptor ligandPolymer chemistryMaterials ChemistryMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryphospheniumPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUS010405 organic chemistryChemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistryphosphine3. Good health0104 chemical sciencesPentaneYield (chemistry)rhodiumelectronic propertiesPhosphine

description

Abstract The coordination properties of a donor stabilized-phosphenium adduct have been examined in rhodium chemistry. The preparation as well as the characterization of the first examples of donor stabilized-phosphenium rhodium(I) complexes is reported in this paper. Indeed, mono- and di-cationic rhodium complexes were obtained in quantitative yield by the direct addition of this imidazolium P(III)-ligand to [RhCl(1,5-COD)] 2 in CH 2 Cl 2 solution with a 1:1 P/Rh ratio under argon and 2:1 P/Rh ratio under CO atmosphere, respectively. Crystal structure of the bis-cationic donor stabilized-phosphenium rhodium(I) complex has been obtained from an acetone/pentane mixture. Its molecular structure has revealed a particular arrangement in which the chloride atom is sandwiched between both imidazolium rings as a result of the electrostatic attractive interactions between the electron-deficient heterocarbene moieties and the electron rich halide atom. On the other hand, the basicity of N-donor-phosphenium adducts has been evaluated by measure of the CO stretching frequency in one rhodium complex, and was found halfway between the phosphites and the strong π-acceptor phosphines.

https://hal.archives-ouvertes.fr/hal-00468082