Metal and Ligand Variations in [MX(diimine)(CO)3] (M=Tc, Re) Complexes: Effects on Photocatalytic CO2 Reduction
نویسندگان
چکیده
Two series of complexes MX(diimine)(CO)(3)] (M = Tc, Re) have been prepared, fully characterised and investigated for their ability to act as photocatalysts for the reduction of CO2 to CO. One series consists of complexes with different aromatic diimine ligands while keeping X = Brconstant. The second series describes complexes with diimine = 2,2-bipyridine and variations in the anionic ligand X-. Although numerous complexes of this type have been prepared and investigated before, a systematic study of their photocatalytic activity has not yet been carried out. Electrochemical and spectroscopic characterisation of these complexes has been performed with the objective of better understanding their respective activity in the photocatalytic CO2 reduction. Despite various modifications, catalytic activity is retained for all compounds exhibiting fluorescence, including (TcCl)-Tc-99(bipy)(CO)(3)], whereas nonfluorescing compounds did not convert CO2 to CO. The correlation of catalytic activity and spectroscopic or electrochemical properties such as absorption or emission wavelengths, redox potentials or Stern-Volmer constants for the reductive quenching of the excited complexes is difficult. Nevertheless, the study emphasises the possibility to obtain ReX(CO)(3)(diimine)] complexes with a wide range of physicochemical properties by ligand variations and the great potential of compounds of this class of complexes as inorganic photosensitisers. DOI: https://doi.org/10.1002/ejic.200600166 Posted at the Zurich Open Repository and Archive, University of Zurich ZORA URL: https://doi.org/10.5167/uzh-65733 Submitted Version Originally published at: Kurz, Philipp; Probst, Benjamin; Spingler, Bernhard; Alberto, Roger (2006). Ligand variations in ReX(diimine)(CO)(3)] complexes: Effects on photocatalytic CO2 reduction. European Journal of Inorganic Chemistry, (15):2966-2974. DOI: https://doi.org/10.1002/ejic.200600166 Metal and Ligand Variations in [MX(diimine)(CO)3] (M=Tc, Re) Complexes: Effects on Photocatalytic CO2 Reduction Philipp Kurz, Bernhard Spingler and Roger Alberto Institute of Inorganic Chemistry, University of Zürich, Winterthurerstrasse 190, 8057 Zürich,
منابع مشابه
Rhenium(i) trinuclear rings as highly efficient redox photosensitizers for photocatalytic CO2 reduction† †Electronic supplementary information (ESI) available: Franck–Condon analysis; photochemical one-electron-reduced species formation and characterisation; photophysical, electrochemical and quenching properties of R(4·5) in DMA; photophysical and electrochemical properties of the catalysts; photocatalytic CO2 reduction experiments and additional data. See DOI: 10.1039/c6sc01913g Click here for additional data file.
We developed new cyclic Re(I)-based trinuclear redox photosensitizers with both high oxidation power in the excited state and strong reduction power in the reduced form. These excellent properties were achieved by introducing electron-donating groups on the diimine ligand of the Re(I) metal centre and by connecting each Re(I) unit with polyphenyl–bisphosphine bridging ligands. These Re-rings we...
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