Department of Chemistry and Center for Photochemical Sciences, Bowling Green State University , Bowling Green, Ohio 43403, United States.
J Am Chem Soc. 2013 Sep 25;135(38):14068-70. doi: 10.1021/ja407816f. Epub 2013 Sep 17.
The Cu(I) metal-to-ligand charge-transfer complex, Cu(dsbtmp)2 (dsbtmp = 2,9-di(sec-butyl)-3,4,7,8-tetramethyl-1,10-phenanthroline), exhibits outstanding stability as a visible-light-absorbing photosensitizer in hydrogen-evolving homogeneous photocatalysis. In concert with the Co(dmgH)2(py)Cl water reduction catalyst and N,N-dimethyl-p-toluidine sacrificial donor in 1:1 H2O:CH3CN, this Cu(I) sensitizer remains active even after 5 days of visible-light-pumped (λex = 452 ± 10 nm) hydrogen evolution catalysis. Deuteration studies illustrate that the hydrogen produced from this composition does indeed originate from aqueous protons.
Cu(I) 金属-配体电荷转移配合物 Cu(dsbtmp)2(dsbtmp = 2,9-二(仲丁基)-3,4,7,8-四甲基-1,10-菲咯啉)作为可见光吸收光催化剂,在氢析出均相光催化中表现出优异的稳定性。在 1:1 H2O:CH3CN 中与 Co(dmgH)2(py)Cl 水还原催化剂和 N,N-二甲基-p-甲苯胺牺牲供体协同作用,即使在可见光激发(λex = 452 ± 10nm) 5 天后进行氢析出催化,这种 Cu(I) 敏化剂仍然保持活性。氘代研究表明,该组成产生的氢气确实来自水相质子。