1H NMR relaxometry was applied to investigate dynamic processes in the isotropic liquid, cholesteric, and crystalline phases of the chiral mesogen 4?-butyl-4-(S)-(2-methylbutoxy)azoxybenzene (4ABO5*). To this aim, 1H longitudinal relaxation rates were measured as a function of temperature (between 257 and 319 K) and Larmor frequency (from 10 kHz to 35 MHz by a fast field-cycling relaxometer and at 400 MHz by an NMR spectrometer). The NMR relaxation dispersion (NMRD) curves so obtained were analyzed in terms of models suitable for the description of dynamic processes in the different phases, thus quantitatively determining values of characteristic motional parameters. In particular, internal and overall rotations/reorientations, molecular translational diffusion, and collective motions contribute to relaxation in the isotropic and cholesteric phases, whereas, in the crystalline phase, relaxation is mainly determined by internal motions and molecular reorientations. The results were discussed and compared with those previously obtained on the same compound by dielectric relaxation spectroscopy.

Dynamics of the Chiral Liquid Crystal 4?-Butyl-4-(S)-(2-methylbutoxy)azoxybenzene in the Isotropic, Cholesteric, and Solid Phases: A Fast Field-Cycling NMR Relaxometry Study

Calucci Lucia;Forte Claudia;Geppi Marco;Geppi Marco
2016

Abstract

1H NMR relaxometry was applied to investigate dynamic processes in the isotropic liquid, cholesteric, and crystalline phases of the chiral mesogen 4?-butyl-4-(S)-(2-methylbutoxy)azoxybenzene (4ABO5*). To this aim, 1H longitudinal relaxation rates were measured as a function of temperature (between 257 and 319 K) and Larmor frequency (from 10 kHz to 35 MHz by a fast field-cycling relaxometer and at 400 MHz by an NMR spectrometer). The NMR relaxation dispersion (NMRD) curves so obtained were analyzed in terms of models suitable for the description of dynamic processes in the different phases, thus quantitatively determining values of characteristic motional parameters. In particular, internal and overall rotations/reorientations, molecular translational diffusion, and collective motions contribute to relaxation in the isotropic and cholesteric phases, whereas, in the crystalline phase, relaxation is mainly determined by internal motions and molecular reorientations. The results were discussed and compared with those previously obtained on the same compound by dielectric relaxation spectroscopy.
2016
Istituto di Chimica dei Composti OrganoMetallici - ICCOM -
Liquid Crystals
NMR relaxometry
Fast Field Cycling
Dielectric Relaxation
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/318812
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