The Journal of Physical Chemistry · 1996 · 244 citations · 33 references
Natural SciencesChemistryMaterials ScienceInorganic ChemistryPhysical ChemistrySpectroscopyCoordination ChemistryInorganic MaterialsInorganic SpectroscopyMetal-ligand BondingTransition Metal ChemistryTransition Metal ComplexesCoordinationCoordination GeometryCoordination Geometry DeterminationSpectroscopic Characterization Of Metal-ligand BondsThermal TreatmentZeolite AdsorbentsZeolite AdsorptionZeolites
The characterization of the coordination geometry of copper ions included within zeolites has been carried out with a combination of in-situ XAFS, photoluminescence, and IR measurements in order to obtain a detailed description of the formation of isolated Cu + monomers with planar 3-coordinate or linear 2-coordinate geometry in the zeolite channels by thermal treatment under vacuum. The Cu + ions within the zeolites were found to exist as isolated Cu + monomers and (Cu + −Cu + ) dimers, their relative concentrations strongly depending on the type of zeolite used. With ZSM-5 and mordenite zeolites, most of the copper cations were found to exist as isolated Cu + monomers, in contrast to the case of the Y-zeolite. CO molecules were adsorbed selectively only on isolated Cu + monomers, distorting the coordination geometry to form stable one-on-one Cu + −CO complexes.
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