2D-SOLID STATE NMR-STUDIES OF ULTRASLOW MOTIONS - PHENYLFLIPS AND CHAIN MOTIONS IN THE GLASSY STATE

被引:18
作者
SCHAEFER, D
HANSEN, M
BLUMICH, B
SPIESS, HW
机构
[1] Max-Planck-Institut für Polymerforschung, W-6500 Mainz
关键词
D O I
10.1016/0022-3093(91)90681-U
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The deuteron 2D exchange NMR experiment was applied to study ultraslow molecular reorientations in polymers below the glass transition. Experimental spectra are presented for phenyldeuterated polycarbonate (PC-d4) and an ionene polyelectrolyte [poly-(N, N-dimethylimino)decamethylenetetrafluoroborate] (I-10-Me-BF4), deuterated in the alpha-position of the alkylene chain. In PC the phenylflip motion in the glassy state does not involve rotations by exactly 180-degrees. Instead the reorientational angle distribution (RAD) of this local process is rather ill-defined and changes when mechanical stress is applied to the sample. The chain dynamics in the solid polyelectrolyte can be considered as a motion between fixed ends, due to the strong Coulomb interaction of the ionic centres. No evidence is found for trans-gauche isomerization; instead the spectra exhibit the characteristics of a restricted diffusive motion.
引用
收藏
页码:777 / 780
页数:4
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