The Journal of Physical Chemistry A · 2011 · 15 citations · 33 references
Natural SciencesChemistryPhysicsInorganic ChemistryPhysical ChemistrySpectroscopyChemical ReactionsCoordination ChemistryMolecular Orbital TheoryPhotocatalysisPhotochemical KineticsPhotochemistryCharge-transfer TransitionsElectronic Spectra Of Transition Metal ComplexesMetal-ligand Charge TransferPhotochemical Reaction MechanismsSpectral FeaturesUltraviolet Light ExposureUltraviolet Photochemistry
Irradiation of AuCl(4)(-) and AuCl(2)(OH)(2)(-) in the gas-phase using ultraviolet light (220-415 nm) leads to their dissociation. Observed fragment ions for AuCl(4)(-) are AuCl(3)(-) and AuCl(2)(-) and for AuCl(2)(OH)(2)(-) are AuCl(2)(-) and AuClOH(-). All fragment channels correspond to photoreduction of the gold atom to either Au(II) or Au(I) depending on the number of neutral ligands lost. Fragment branching ratios of AuCl(4)(-) are observed to be highly energy dependent and can be explained by comparison of the experimental data to calculated threshold energies obtained using density functional theory. The main observed spectral features are attributed to ligand-to-metal charge transfer transitions. These results are discussed in the context of the molecular-level mechanisms of Au(III) photochemistry.
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Generalized Gradient Approximation Made Simple
John P. Perdew, Kieron Burke, Matthias Ernzerhof · Physical Review Letters · 1996 · 211.5K citations · Full text
Natural Sciences, Chemistry, Physics +16
Density-functional theory of atoms and molecules
James D. Patterson · Annals of Nuclear Energy · 1989 · 12.6K citations
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