Journal of Polymer Science Part B: Polymer Physics, Vol.33, No.3, 367-378, 1995
Local Chain Motions of Poly(Beta-Hydroxyoctanoate) in the Bulk - C-13 NMR Relaxation Study
Variable-temperature C-13 NMR spin-lattice relaxation times (T-1) and Nuclear Overhauser Enhancements (NOE) at two magnetic fields have been used to study the dynamics of the amorphous part of a semicrystalline sample (33% of crystallinity) of poly(beta-hydroxyoctanoate) (PHO). The interpretation of the relaxation data of the backbone carbons was made by employing a number of motional models. Among these, the DLM model offered the best interpretation of the relaxation data in terms of conformational transitions and librational motions of the backbone C - H vectors, and proved to be superior to unimodal distribution functions. The interpretation of temperature- and frequency-dependent T-1 and NOE data of the carbon nuclei in the n-pentyl side chain was made by employing a newly developed composite spectral density function for multiple internal C - C bond rotations of restricted amplitude and chain segmental motion. The temperature dependence of the linewidths of the various protonated carbon resonances of PHO has been discussed in terms of the semicrystalline character of this polymer.
Keywords:GLASS-TRANSITION TEMPERATURE;NUCLEAR MAGNETIC-RELAXATION;TIME-CORRELATION FUNCTIONS;SPIN-LATTICE RELAXATION;TETRACHLOROETHANE SOLUTION;MOLECULAR-MOTION;POLYMERS;DYNAMICS;STATE;WELL