Mononuclear and dinuclear heteroleptic Cu(I) complexes based on pyridyl-triazole and DPEPhos with long-lived excited-state lifetimes

被引:13
作者
Bizzarri, Claudia [1 ]
Arndt, Andreas P. [2 ]
Kohaut, Stephan [3 ]
Fink, Karin [3 ]
Nieger, Martin [4 ]
机构
[1] Karlsruhe Inst Technol, Inst Organ Chem, Fritz Haber Weg 6, D-76131 Karlsruhe, Germany
[2] Karlsruhe Inst Technol, Light Technol Inst, Karlsruhe, Germany
[3] Karlsruhe Inst Technol, Inst Nanotechnol, Karlsruhe, Germany
[4] Univ Helsinki, Dept Chem, Helsinki, Finland
关键词
Heteroleptic Copper(I) complexes; photosensitizers; carbon dioxide reduction; Ster-Volmer quenching; cooperativity; PHOTOCATALYTIC HYDROGEN-PRODUCTION; TRANSFER RADICAL-ADDITION; GAUSSIAN-BASIS SETS; COPPER(I) COMPLEXES; C-C; PHOTOPHYSICAL PROPERTIES; PHOTOREDOX CATALYSIS; METAL-COMPLEXES; ATOMS LI; LIGHT;
D O I
10.1016/j.jorganchem.2018.07.013
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A mononuclear and two dinuclear heteroleptic Cu(I) complexes have been successfully prepared, using the chelating bis [(2-diphenylphosphino)phenyl] ether (DPEPhos) and pyrid-2'-yl-1H-1,2,3-triazole as chelating ligands. They show good luminescence in solution at room temperature with long-lived excited states. Furthermore, bimolecular quenching experiments of these new complexes with the catalyst Ni(cyclam)Cl-2 encourage the use of such compounds as photosensitizers for the photoreduction of carbon dioxide. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:140 / 149
页数:10
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