Towards hydrogen evolution initiated by LED light: 2-(1H-1,2,3-Triazol-4-yl)pyridine-containing polymers as photocatalyst.
Macromol Rapid Commun
; 36(7): 671-7, 2015 Apr.
Article
em En
| MEDLINE
| ID: mdl-25656046
ABSTRACT
Two- and three-component polymethacrylates, featuring a 2-(1-substituted-1H-1,2,3-triazol-4-yl)pyridine-based metal complex as photosensitizer, a viologen-type electron mediator, and a triethylene glycol methyl ether as solubilizing part are synthesized by statistical reversible addition-fragmentation chain transfer (RAFT) radical polymerization allowing the construction of well-defined copolymers. Thereby, heteroleptic ruthenium(II) and iridium(III) complexes serve as charged photosensitizers. In hydrogen evolution experiments, as proof-of-concept, triethylamine is utilized as a sacrificial donor and colloidal platinum as hydrogen evolving catalyst. The macromolecules bearing heteroleptic iridium(III) complexes of the general formula [Ir(ppy)2 (trzpy)]PF6 (ppy 2-phenylpyridine; trzpy 2-(1-substituted-1H-1,2,3-triazol-4-yl)pyridine) and [Ir(btac)2 (trzpy)]PF6 (btac 3-(2-benzothiazolyl)-7-(diethylamino)coumarin) are photocatalytically active producing molecular hydrogen in water upon illumination at 470 nm. By changing the cyclometalating ligand from ppy to btac, the photocatalytic performance of the copolymer as reflected in the turnover number increases by two orders of magnitude.
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MEDLINE
Assunto principal:
Polímeros
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Piridinas
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Triazóis
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Fármacos Fotossensibilizantes
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Hidrogênio
Idioma:
En
Ano de publicação:
2015
Tipo de documento:
Article