3d Element Complexes of Pentadentate Bipyridine-Pyridine-Based Ligand Scaffolds: Structures and Photocatalytic Activities

被引:90
作者
Bachmann, Cyril [1 ]
Guttentag, Miguel [1 ]
Spingler, Bernhard [1 ]
Alberto, Roger [1 ]
机构
[1] Univ Zurich, Inst Inorgan Chem, CH-8057 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
DRIVEN HYDROGEN-PRODUCTION; SOLAR-ENERGY; COBALOXIME CATALYSTS; GENERATING HYDROGEN; HYDROXIDE COMPLEX; WATER; COBALT; REDUCTION; EVOLUTION; SYSTEM;
D O I
10.1021/ic4004017
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The synthesis of the two penta-pyridyl type ligands pyridine-2,6-diylbis(dipyridin-2-ylmethanol) (PPy, 1) and bis-2,2 ''-bipyridine-6-yl(pyridine-2-yl)methanol (aPPy, 2) is described. Both ligands coordinate rapidly to the 3d element cations Mn-II, Fe-II, Co-II, Ni-II, Cu-II, and Zn-II, thereby yielding complexes of the general composition [MBr(1)](+) and [MBr(2)](+), respectively. Further, the X-ray structures of selected complexes with ligands 1 and 2 are described. They show metal center dependent structural features and complexes with 2 exhibiting distinctly distorted octahedral geometries. Moreover, photocatalytic water reduction with [(CoBr)-Br-II(PPy)]Br (1c) and [(CoBr)-Br-II(aPPy)]Br (2c) as water reducing catalysts (WRC) was investigated. Both complexes showed catalytic activity in water when in presence of ascorbic acid as sacrificial electron donor and [Re(py)(bpy)(CO)(3)](+) (3) as photosensitizer (PS). Turnover numbers, TONs (H-2/Co), up to 11 000 were achieved. Complex 2c was more active than 1c, whereas none of the other complexes showed any activity.
引用
收藏
页码:6055 / 6061
页数:7
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