| Autor: |
Geoghegan BL; Max Planck Institute for Chemical Energy Conversion, Stiftstrasse 34-36, 45470 Mülheim an der Ruhr, Germany. george.cutsail@cec.mpg.de.; Institute of Inorganic Chemistry, University of Duisburg-Essen, Universitätsstrasse 5-7, 45117 Essen, Germany.; Department of Chemistry, Imperial College London, Molecular Sciences Research Hub, W12 0BZ, London, UK., Bilyj JK; School of Chemistry and Molecular Biosciences, University of Queensland, Brisbane 4072, Australia., Bernhardt PV; School of Chemistry and Molecular Biosciences, University of Queensland, Brisbane 4072, Australia., DeBeer S; Max Planck Institute for Chemical Energy Conversion, Stiftstrasse 34-36, 45470 Mülheim an der Ruhr, Germany. george.cutsail@cec.mpg.de., Cutsail GE 3rd; Max Planck Institute for Chemical Energy Conversion, Stiftstrasse 34-36, 45470 Mülheim an der Ruhr, Germany. george.cutsail@cec.mpg.de.; Institute of Inorganic Chemistry, University of Duisburg-Essen, Universitätsstrasse 5-7, 45117 Essen, Germany. |
| Abstrakt: |
This study investigates the influence of ligand charge on transition energies in a series of CuN 2 S 2 complexes based on dithiocarbazate Schiff base ligands using Cu K-edge X-ray absorption spectroscopy (XAS) and Kβ valence-to-core (VtC) X-ray emission spectroscopy (XES). By comparing the formally Cu(II) complexes [CuII(HL1)] (HL1 2- = dimethyl pentane-2,4-diylidenebis[carbonodithiohydrazonate]) and [CuII(HL2)] (HL2 2- = dibenzyl pentane-2,4-diylidenebis[carbonodithiohydrazonate]) and the formally Cu(III) complex [CuIII(L2)], distinct changes in transition energies are observed, primarily attributed to the metal oxidation state. Density functional theory (DFT) calculations demonstrate how an increased negative charge on the deprotonated L2 3- ligand stabilizes the Cu(III) center through enhanced charge donation, modulating the core transition energies. Overall, significant shifts to higher energies are noted upon metal oxidation, emphasizing the importance of scrutinizing ligand structure in XAS/VtC XES analysis. The data further support the redox-innocent role of the Schiff base ligands and underscore the criticality of ligand protonation levels in future spectroscopic studies, particularly for catalytic intermediates. The combined XAS-VtC XES methodology validates the Cu(III) oxidation state assignment while offering insights into ligand protonation effects on core-level spectroscopic transitions. |
