Nylon 6 structure in solid state as studied by high‐resolution 13C‐NMR spectroscopy

High resolution 13C‐NMR spectra of nylon 6 samples crystallized under various conditions and of a drawn sample were measured at room temperature by the cross polarization/magic angle spinning (CP/MAS) and pulse saturation transfer/magic angle spinning techniques. Additionally, 13C‐NMR spectra of the drawn sample were measured at temperatures from 20 to 100°C by the CP/MAS technique and at 20 and 100°C by the low‐power decoupling/magic angle spinning technique. The nylon 6 structure in the solid‐state is discussed on the basis of these results. The solid‐state 13C chemical shift data are used for reference in a study of conformation in solution.