Hinze G, Haase M, Nolde F, Müllen K, Basché Th
Institute for Physical Chemistry, Johannes Gutenberg-University, Jakob-Welderweg 11, D-55099 Mainz, Germany.
J Phys Chem A. 2005 Aug 4;109(30):6725-9. doi: 10.1021/jp0521003.
We have investigated electronic excitation energy transfer in a specifically designed bichromophoric donor/acceptor dyad in which the donor (perylenediimide) and acceptor (terrylenediimide) are linked by a rigid heptaphenyl-spacer. Because of the choice of the bridge, which defines the distance and orientation of the two chromophores, donor as well as acceptor emission is observed. The significantly smaller photostability of the donor allows for time-resolved measurements of the acceptor emission at the single-molecule level with and without energy transfer from the donor. By analyzing the differences of the rise/decay profiles for both pathways, we could determine time constants of energy transfer with high accuracy for single dyads. The results show that the experimental approach presented here works even for situations in which the energy transfer times are smaller than the temporal resolution of the detection system.
我们研究了一种经过特殊设计的双色团供体/受体二元体系中的电子激发能量转移,其中供体(苝二酰亚胺)和受体(并四苯二酰亚胺)通过刚性的七苯基间隔基相连。由于桥连基团的选择决定了两个发色团的距离和取向,因此同时观察到了供体和受体的发射。供体显著较低的光稳定性使得在有和没有来自供体的能量转移的情况下,都能够在单分子水平上对受体发射进行时间分辨测量。通过分析两种途径的上升/衰减曲线差异,我们能够高精度地确定单个二元体系的能量转移时间常数。结果表明,本文提出的实验方法即使在能量转移时间小于检测系统的时间分辨率的情况下也能奏效。