
Journal of Physical Chemistry p. 711 - 716 (1984)
Update date:2022-08-11
Topics:
Chao, J.
Desando, M. A.
Gourlay, D. L.
Orr, D. E.
Walker, S.
Several symmetrically substituted diaryl ethers have been studied in a polystyrene matrix and bis(4-nitrophenyl) ether also in glassy o-terphenyl by dielectric adsorption techniques in the frequency range 10-1E5 Hz over temperatures of 77-323 K.Bis(4-cyanophenyl) ether in polystyrene was also examined at many temperatures in the frequency range E-4-E-7Hz.In the polystyrene matrix both the molecular and intramolecular relaxation processes were detected for diphenyl ether and bis(4-nitrophenyl) ether.An intramolecular relaxation process was detected for most of the aromatic ethers, and the associated Eyring enthalpy of activation is ca. 10 kJ mol-1.Which is similar to that observed for some alkyl aryl ethers in the same media.The present work establishes that the energy barrier for rotation around the C-O bonds is symmetrically substituted diphenyl ethers is very low and that intramolecular motion would be expected to occur quite readily about these bonds.
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