School of Chemical Sciences, University of Illinois, Urbana, Illinois 61801, United States.
J Am Chem Soc. 2012 Mar 14;134(10):4525-8. doi: 10.1021/ja211778j. Epub 2012 Feb 27.
The diiron hydride (μ-H)Fe(2)(pdt)(CO)(4)(dppv) (H2, dppv = cis-1,2-C(2)H(2)(PPh(2))(2)) is shown to be an effective photocatalyst for the H(2) evolution reaction (HER). These experiments establish the role of hydrides in photocatalysis by biomimetic diiron complexes. Trends in redox potentials suggests that other unsymmetrically substituted diiron hydrides are promising catalysts. Unlike previous catalysts for photo-HER, H2 functions without sensitizers: irradiation of H2 in the presence of triflic acid (HOTf) efficiently affords H(2). Instead of sacrificial electron donors, ferrocenes can be used as recyclable electron donors for the photocatalyzed HER, resulting in 4 turnovers.
[(μ-H)Fe2(pdt)(CO)4(dppv)]+(H2+,dppv = cis-1,2-C2H2(PPh2)2)被证明是氢气生成反应 (HER) 的有效光催化剂。这些实验确立了仿生二铁配合物中氢化物在光催化中的作用。氧化还原电位的趋势表明,其他不对称取代的二铁氢化物是有前途的催化剂。与之前的光 HER 催化剂不同,[H2]+无需敏化剂即可发挥作用:在三氟甲磺酸 (HOTf) 的存在下辐照 [H2]+可有效地得到 H2。与牺牲电子供体不同,二茂铁可用作光催化 HER 的可回收电子供体,从而实现 4 次周转。