A. Isogai et al., SOLID-STATE CP MAS C-13-NMR ANALYSIS OF CELLULOSE AND TRI-O-SUBSTITUTED CELLULOSE ETHERS/, Carbohydrate polymers, 21(4), 1993, pp. 277-281
Highly crystalline tri-O-substituted cellulose ethers having ethyl, n-
propyl, n-butyl, allyl, and methallyl substituents were prepared from
low-molecular weight cellulose (DP = 15). Influences of conformational
and packing effects on solid-state C-13-NMR spectra were studied by u
sing X-ray diffraction and solid- and solution-state C-13-NMR analyses
of the cellulose derivatives. Unit-cell sizes tentatively obtained fr
om X-ray diffraction patterns of the cellulose derivatives indicated t
hat conformations and packing states of cellulose chains and alkyl cha
ins of substituents were different between the derivatives. Solid- and
solution-state C-13-NMR spectra of cellulose allomorphs, and effects
of hydrogen bonds present in celluloses I, II, and III on chemical shi
fts of their solid-state C-13-NMR spectra were proposed.