Light-Harvesting Three-Chromophore Systems Based on Biphenyl-Bridged Periodic Mesoporous Organosilica

被引:35
作者
Groesch, Lyubov [1 ]
Lee, Young Joo [1 ]
Hoffmann, Frank [1 ]
Froeba, Michael [1 ]
机构
[1] Univ Hamburg, Inst Inorgan Chem, D-20746 Hamburg, Germany
关键词
chromophores; donor-acceptor systems; fluorescence spectroscopy; organic-inorganic hybrid; mesoporous materials; RESONANCE ENERGY-TRANSFER; METAL-ORGANIC FRAMEWORKS; FLUORESCENT J-DIMERS; MESOSTRUCTURED ORGANOSILICA; OLIGO(P-PHENYLENE VINYLENE)S; SUPRAMOLECULAR ASSEMBLIES; ARTIFICIAL PHOTOSYNTHESIS; SILICA-GELS; EMISSION; HYBRIDS;
D O I
10.1002/chem.201403393
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Three-chromophore systems with light-harvesting behavior were prepared, which are based on periodic mesoporous organosilica (PMO) with crystal-like ordered structure. The organic bridges of biphenyl-PMO in the pore walls act as donors and two types of dye are incorporated in the one-dimensional channels. Consecutive two-step-Forster resonance energy transfer is observed from the biphenyl moieties to mediators (diethyl-aminocoumarin or aminoacridone), followed by energy transfer from mediators to acceptors (dibenzothiacarbocyanine, indodicarbocyanine, sulforhod-amine G). High energy-transfer efficiencies ranging from 70 to 80% are obtained for two-step-FRET, indicating that the mesochannel structure with one-dimensional ordering provides spatial arrangement of chromophore pairs for an efficient direct energy transfer. The emission wavelength can be tuned by a choice of acceptor dye: 477 nm (diethylaminocoumarin), 519 nm (aminoacridone), 567 nm (sulforhodamine G), 630 nm (dibenzothiacarbocyanine), and 692 nm (indodicarbocyanine).
引用
收藏
页码:331 / 346
页数:16
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