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Energy transfer mediated by asymmetric hydrogen-bonded interfaces.

ABSTRACT: Amidine-appended ferrocene derivatives form a supramolecular assembly with Ru(ii)(bpy-COOH) (L)22+ complexes (bpy-COOH is 4-CO2H-4'-CH3-bpy and L = bpy, 2,2'-bipyridine or btfmbpy, 4,4'-bis (trifluoromethyl)-2,2'-bipyridine). Steady-state, time-resolved spectroscopy and kinetic isotope effects establish that the metal-to-ligand charge transfer excited states of the Ru(ii) complexes are quenched by proton-coupled energy transfer (PCEnT). These results show that proton motion can be effective in mediating not only electron transfer (ET) but energy transfer (EnT) as well.

SUBMITTER: Young ER

PROVIDER: S-EPMC3868475 | biostudies-literature | 2012 Feb

REPOSITORIES: biostudies-literature

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Energy transfer mediated by asymmetric hydrogen-bonded interfaces.

Young Elizabeth R ER Rosenthal Joel J Nocera Daniel G DG

Chemical science 20120201 2

Amidine-appended ferrocene derivatives form a supramolecular assembly with Ru(ii)(bpy-COOH) (L)22+ complexes (bpy-COOH is 4-CO2H-4'-CH3-bpy and L = bpy, 2,2'-bipyridine or btfmbpy, 4,4'-bis (trifluoromethyl)-2,2'-bipyridine). Steady-state, time-resolved spectroscopy and kinetic isotope effects establish that the metal-to-ligand charge transfer excited states of the Ru(ii) complexes are quenched by proton-coupled energy transfer (PCEnT). These re ...[more]

PMID: 24363889

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