Structural Characterization of Supported Rh^I(CO)₂/γ-Al₂O₃ Catalysts by Periodic DFT Calculations

Abstract

Microscopic structures of monodispersed rhodium dicarbonyl species chemisorbed on a ceramic metal-oxide support (γ-alumina) have been obtained by density functional theory (DFT) calculations with periodic boundary conditions applied. Several minimum energy structures of species were obtained and their relative energies indicate that, in the most energetically stable geometry, the rhodium atom is coordinated in a square-planar environment and forms a four-membered Rh–O–Al–O ring, with one Al atom octahedrally coordinated. Another docking geometry, close lying in energy, also has a square-planar coordination for the rhodium atom and involves a six-membered Rh–O–Al–O–Al–O ring with one Al octahedrally coordinated and one Al tetrahedrally coordinated. Computed bond lengths were found to be in reasonable agreement with experimental bond lengths as determined by EXAFS spectroscopy. Theoretical Rh K-edge XANES spectra suggest that the pre-edge region probes electronic states localized on the Rh^I(CO)₂ unit, while postedge features probe the electronic states arising from the Rh^I(CO)₂ interaction with the support, which partly depends on the docking geometry of the Rh^I(CO)₂ units