Probing photophysical processes in individual multichromophoric dendrimers by single-molecule spectroscopy

被引:221
作者
Hofkens, J
Maus, M
Gensch, T
Vosch, T
Cotlet, M
Köhn, F
Herrmann, A
Müllen, K
De Schryver, F
机构
[1] Katholieke Univ Leuven, Dept Chem, BE-3001 Heverlee, Belgium
[2] Max Planck Inst Polymer Res, G-55128 Mainz, Germany
关键词
D O I
10.1021/ja0012570
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Individual multichromophoric dendrimer molecules, bearing eight perylenecarboximide chromophores at the rim, immobilized in a thin polyvinylbutyral (PVB) film were studied by far-field fluorescence microscopy. Fluorescence intensity trajectories as a function of time (transients), spectra, and decay traces were recorded separately or simultaneously. For comparison, similar measurements have been performed on a model compound containing one perylenecarboximide chromophore. Collective on/off jumps of the fluorescence intensity were observed for single dendrimer molecules, resembling previously reported collective jumps for the emission of single light-harvesting antenna systems. Spectra and decays of both non-interacting and dimer-like interacting chromophoric sites could be distinguished within an individual dendrimer. Transitions between the different spectral forms and decay times, observed for a single molecule, underline the dynamic character of the interactions among the chromophores. Evidence for a stepwise bleaching process of the multichromophoric system was found. Furthermore, the single-molecule data incontestably prove the assumptions stated in the ensemble model.
引用
收藏
页码:9278 / 9288
页数:11
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