Self-Assembled Cofacial Zinc-Porphyrin Supramolecular Nanocapsules as Tuneable 1O2 Photosensitizers

被引:28
|
作者
Colomban, Cedric [1 ]
Fuertes-Espinosa, Carles [1 ]
Goeb, Sebastien [2 ]
Salle, Marc [2 ]
Costas, Miquel [1 ]
Blancafort, Lluis [1 ]
Ribas, Xavi [1 ]
机构
[1] Univ Girona, Dept Quim, IQCC, Campus Montilivi, E-17003 Girona, Catalonia, Spain
[2] Univ Angers, Lab MOLTECH Anjou, CNRS, UMR 6200, 2 Bd Lavoisier, F-49045 Angers, France
关键词
host-guest systems; porphyrins; self-assembly; singlet oxygen; supramolecular photosensitizers; COBALT-PORPHYRIN; TETRAPHENYLPORPHYRIN DERIVATIVES; PHOTODYNAMIC THERAPY; WATER OXIDATION; OXYGEN; GENERATION; HYDROFORMYLATION; PHOTOOXIDATION; DEACTIVATION; CATALYST;
D O I
10.1002/chem.201705531
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We demonstrate the benefits of using cofacial Zn-porphyrins as structural synthons in coordination-driven self-assembled prisms to produce cage-like singlet oxygen (O-1(2)) photosensitizers with tunable properties. In particular, we describe the photosensitizing and emission properties of palladium- and copper-based supramolecular capsules, and demonstrate that the nature of the bridging metal nodes in these discrete self-assembled prisms strongly influences O-1(2) generation at the Zn-porphyrin centers. The Pd-II-based prism is a particularly robust photosensitizer, whereas the Cu-II self-assembled prism is a dormant photosensitizer that could be switched to a ON state upon disassembly of the suprastructure. Furthermore, the well-defined cavity within the prisms allowed encapsulation of pyridine-based ligands and fullerene derivatives, which led to a remarkable guest tuning of the O-1(2) production.
引用
收藏
页码:4371 / 4381
页数:11
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