CORRELATIONS OF RELAXING DIPOLE ENTITIES AND CONDUCTIVITY EFFECTS ON MODEL COMPOUNDS AND MOLECULAR CHAINS WITH 2-CHLOROCYCLOHEXYL ESTERS INTHEIR STRUCTURE
R. Diazcalleja et al., CORRELATIONS OF RELAXING DIPOLE ENTITIES AND CONDUCTIVITY EFFECTS ON MODEL COMPOUNDS AND MOLECULAR CHAINS WITH 2-CHLOROCYCLOHEXYL ESTERS INTHEIR STRUCTURE, Macromolecules, 27(8), 1994, pp. 2092-2101
The temperature and frequency dependence of the complex dielectric per
mittivity epsilon for both 2-chlorocyclohexyl isobutyrate (CCHI) and
poly(2-chlorocyclohexyl acrylate) (PCCHA) is reported. The polymer exh
ibits an ostensible beta relaxation, centered at -60-degrees-C at 5 Hz
, whose activation energy at constant frequency seems to increase with
temperature followed by a glass-rubber relaxation or a process, cente
red at 70-degrees-C at 5 Hz, in which conductive processes become domi
nant at low frequencies. The model compound only exhibits a glass-liqu
id relaxation whose maximum is located at -92-degrees-C at 1 Hz. The a
nalysis of the dielectric results in terms of the electric modulus sug
gests that whereas the conductive processes in CCHI are produced only
by free charges, the conductivity observed in PCCHA involves both free
charges and interfacial phenomena. The experimental intramolecular di
polar correlation g(intra) is somewhat larger than 1 for both CCHI and
PCCHA, suggesting that correlations of orientation enhance the polari
ty of these systems. A 4 X 4 rotational states scheme which accounts f
or two rotational states about the CH-CO bonds of the side group repro
duces very satisfactorily the intramolecular correlation coefficient o
f the polymer. Finally, the critical interpretation of the dielectric
results obtained in the bulk indicates that intermolecular dipolar int
eractions do not play a significant role in the dielectric behavior of
these systems.