Abstract
We have studied details of the molecular origin of slow secondary relaxation near in a series of neat polyalcohols by means of dielectric spectroscopy and NMR. From glycerol to threitol, xylitol, and sorbitol the appearance of the secondary relaxation changes gradually from a wing-type scenario to a pronounced peak. It is found that in sorbitol the dynamics of the whole molecule contributes equally to the process, while in glycerol the hydrogen bond forming OH groups remain rather rigid compared to the hydrogens bonded to the carbon skeleton.
- Received 10 August 2001
DOI:https://doi.org/10.1103/PhysRevLett.88.095701
©2002 American Physical Society