1991
DOI: 10.1021/ma00021a016
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On the dielectric properties of poly(glutamic acid) in aqueous solution in the frequency range 107-1010 Hz

Abstract: The permittivity spectra of aqueous poly(g1utamic acid) and adenosine triphosphate solutions have been measured by the dielectric time domain spectroscopy technique in the frequency range of 20 MHz to 5 GHz. No evidence of a reported dispersion in the 100-MHz region due to side-group motions in poly-(glutamic acid) was found. It is demonstrated experimentally and shown theoretically that the premature truncation of time domain line shapes may introduce seeming dispersions, the frequency region of which will de… Show more

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Cited by 6 publications
(6 citation statements)
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“…If the polymer is a rodlike polymer, we get ( |, (0) |"(0) = µ"2( cos2 0)0|,(í;n) (11) where 0 is the angle between the helical axis and the parallel component of each dipole. In the case of PGA, it changes from the randomly coiled polymer at fc = 1 to the rodlike polymer at /c = 0, and its fraction of the coiled part changes accordingly with the pH value.…”
Section: Discussionmentioning
confidence: 99%
“…If the polymer is a rodlike polymer, we get ( |, (0) |"(0) = µ"2( cos2 0)0|,(í;n) (11) where 0 is the angle between the helical axis and the parallel component of each dipole. In the case of PGA, it changes from the randomly coiled polymer at fc = 1 to the rodlike polymer at /c = 0, and its fraction of the coiled part changes accordingly with the pH value.…”
Section: Discussionmentioning
confidence: 99%
“…[1][2][3][4] Dielectric spectroscopy in the high-frequency region (up to some GHz) has been extensively used to characterize the dielectric relaxation due to dipolar orientational polarization associated the with side-chain dynamics. [5][6][7] In an our recent work, 8 we have investigated the high-frequency dielectric properties of two different polypeptides [poly(␣-glutamate) and poly(␥-glutamate)] in aqueous solutions, and the observed dielectric dispersion, located at about 50 -100 MHz, has been attributed to the micro-Brownian motion of the side-chain groups along the chain of these polymers.…”
Section: Introductionmentioning
confidence: 99%
“…On the other hand, looking from the complementary side, the fall in the normalized relaxation strengths of two of the B components, namely nB and rB (Fig. 3), indicates a structure breaking effect of Gly on these self-associating mono-alcohols, an explanation which has similarly been given for the addition of diols to normal alcohols [2]. A tendency to form hetero-complexes with a molar A : B ratio of about 1.3 may be inferred from the plots.…”
Section: Discussionmentioning
confidence: 63%