Solid-state 19F MAS NMR study on the conformation and molecular mobility of poly(chlorotrifluoroethylene)

Hiroto Tatsuno; Keitaro Aimi; Shinji Ando

doi:10.1002/mrc.1982

Solid-state 19F MAS NMR study on the conformation and molecular mobility of poly(chlorotrifluoroethylene)

Magn Reson Chem. 2007 May;45(5):401-9. doi: 10.1002/mrc.1982.

Authors

Hiroto Tatsuno¹, Keitaro Aimi, Shinji Ando

Affiliation

¹ Department of Organic and Polymeric Materials, Tokyo Institute of Technology, Ookayama, Meguro-ku, Tokyo 152-8552, Japan.

PMID: 17372960
DOI: 10.1002/mrc.1982

Abstract

The temperature dependence of molecular mobility and conformational changes of poly(chlorotrifluoro- ethylene) (PCTFE) have been investigated by solid-state (19)F magic angle spinning (MAS) NMR spectroscopy. The pulse techniques of dipolar-filter and T(1rho)-filter allow selective observation of the amorphous and crystalline domains, respectively. The temperature dependence of T(1rho) (F) revealed that the segmental motion in the amorphous domain becomes vigorous above ca 80 degrees C, which is well above the glass transition (T(g)) temperature (52 degrees C) and more close to the beta-relaxation temperature (95 degrees C). On the other hand, vigorous molecular motions in the crystalline domain occur above 120 degrees C, which is much below the melting temperature (212 degrees C). This indicates that the polymer chains in the PCTFE crystallites are more mobile than those of typical semicrystalline fluoropolymers like poly(vinylidene fluoride) (PVDF), which can be associated with structural imperfections in the crystallites. In addition, the density functional theory (DFT) calculations of (19)F magnetic shielding suggest that the high-frequency shifts observed for the crystalline signals above 80 degrees C can be ascribed to the conformational change around meso diads toward more twisted and/or helical conformations in the main chain.