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Development of Palladium L-edge X-ray Absorption Spectroscopy and Its Application on Chloro Palladium Complexes

出版	Montana State University--Bozeman, 2005
URL	http://books.google.com.hk/books?id=M17CjwEACAAJ&hl=&source=gbs_api

註釋X-ray Absorption Spectroscopy (XAS) is a synchrotron-based experimental technique that can provide information about geometric and electronic structures of transition metal complexes with unoccupied d orbitals. Combination of metal L-edge and ligand K-edge XAS has the potential to define the experimental ground state electronic structure. We developed a quantitative treatment for Pd L-edge spectroscopy based on the already established Cl K-edge XAS for a series of chloro palladium complexes, which are precatalysts in numerous organic transformations. We found that Pd-Cl bonds are highly covalent (23% per Cl in [PdCl4]2−, 34% per Cl in [PdCl6]2−, and 46% in PdCl2). Dipole integrals for Pd(2p.4d) transitions of 42 eV for Pd(II) and 48 eV for Pd(IV) LIII-edges and 39 eV and 35 eV, respectively, at these Pd oxidation states for the LII-edges were determined. Application of the metal-ligand covalencies and transition dipole integrals by describing the ground state bonding in PdCl2 with bridging Cl ligands was demonstrated. In future studies, a similar approach will be utilized for palladium phosphine, allyl, olefin complexes in order to define their experimental electronic structure and correlate this with their observed reactivity.