Highly efficient supramolecular photocatalysts for CO2 reduction using visible light

被引:120
|
作者
Sato, Shunsuke
Koike, Kazuhide
Inoue, Haruo
Ishitani, Osamu
机构
[1] Tokyo Inst Technol, Dept Chem, Grad Sch Sci & Engn, Meguro Ku, Tokyo 1528551, Japan
[2] Natl Inst Adv Ind Sci & Technol, Tsukuba, Ibaraki 3058569, Japan
[3] Tokyo Metropolitan Univ, Dept Appl Chem, Grad Sch Urban Environm Sci, Hachioji, Tokyo 1920397, Japan
[4] JST, CREST, Kawaguti, Saitama 3320012, Japan
关键词
D O I
10.1039/b613419j
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We report the most efficient homogeneous photocatalyst yet for CO2 reduction using a wide range of visible-light wavelength. We synthesized new Ru(II)-Re(I) binuclear complexes with 1,3-bis(4'-methyl[2,2']bipyridinyl-4-yl)-propan-2-ol (bpyC3bpy) as a bridge ligand, specifically [Ru-ReP(OEt)(3)](3+) and [Ru-Repy](3+) where a P(OEt)(3) or pyridine ligand coordinates on the Re site. Their photocatalytic activities were compared with [Ru-ReCl](2+), which has a Cl- ligand on the Re site and has recently been reported as a much better photocatalyst (Phi = 0.12, TNCO = 160) than a 1 : 1 mixed system of the corresponding Ru(II) and Re(I) mononuclear complexes. The best photocatalyst was [Ru-ReP(OEt)(3)](3+), for which Phi = 0.21 and TNCO = 232. A mechanistic study clearly showed that [Ru-ReP(OEt)(3)](3+) is rapidly converted into the solvento complex [Ru-ReSol](3+), (Sol = DMF or TEOA) which is the actual photocatalyst. Although similar rapid ligand substitution occurs with other supramolecules, the pyridine and Cl- anions accelerate the decomposition of the supramolecular photocatalysts.
引用
收藏
页码:454 / 461
页数:8
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