Single Molecule Probing of the Local Segmental Relaxation Dynamics in Polymer above the Glass Transition Temperature

被引:34
作者
Braeken, Els [2 ,3 ]
De Cremer, Gert [2 ,3 ]
Marsal, Philippe [4 ]
Pepe, Gerard [4 ]
Muellen, Klaus [5 ]
Vallee, Renaud A. L. [1 ]
机构
[1] CNRS, Ctr Rech Paul Pascal, UPR 8641, F-33600 Pessac, France
[2] Katholieke Univ Leuven, Dept Chem, B-3001 Heverlee, Belgium
[3] Katholieke Univ Leuven, Inst Nanoscale Phys & Chem, B-3001 Heverlee, Belgium
[4] CNRS, Ctr Interdisciplinaire Nanosci Marseille, UPR 3118, F-13288 Marseille 09, France
[5] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
关键词
SPATIALLY HETEROGENEOUS DYNAMICS; T-G; DIELECTRIC-RELAXATION; FLUORESCENCE LIFETIME; ROTATIONAL DIFFUSION; POLYSTYRENE; SPECTROSCOPY; EMISSION; MOTIONS; REORIENTATION;
D O I
10.1021/ja901636v
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We investigate the temporal dynamics of terrylene diimide molecule with four phenoxy rings (TDI) in a poly(styrene) (PS) matrix in the supercooled regime by use of single molecule spectroscopy. By recording both fluorescence lifetime and linear dichroism observables simultaneously, we show that the TDI dye molecule is a versatile probe of the local dynamics in the polymer. The molecule is able to undergo conformational changes, as indicated by lifetime fluctuations and/or reorientation jumps, as indicated by both observables on different time scales. Owing to molecular mechanics and quantum calculations, we could assign the conformational changes to folding/unfolding event(s) of one or more arms with respect to the conjugated core. We tentatively attribute the different spatial extents of the locally probed motions to the a and 0 relaxation processes occurring in the PS matrix.
引用
收藏
页码:12201 / 12210
页数:10
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