TY - JOUR
T1 - Dielectric spectra broadening as a signature for dipole-matrix interaction. III. Water in adenosine monophosphateadenosine-5′-triphosphate solutions
AU - Puzenko, Alexander
AU - Levy, Evgeniya
AU - Shendrik, Andrey
AU - Talary, Mark S.
AU - Caduff, Andreas
AU - Feldman, Yuri
N1 - Funding Information:
This work has been supported by the Israel Science Foundation (ISF) (Grant No. 465/11).
PY - 2012/11/21
Y1 - 2012/11/21
N2 - In this, the third part of our series on the dielectric spectrum symmetrical broadening of water, we consider the nucleotide aqueous solutions. Where in Parts I [E. Levy, J. Chem. Phys. 136, 114502 (2012)10.1063/1.3687914] and II [E. Levy, J. Chem. Phys. 136, 114503 (2012)10.1063/1.3691183], the dipole-dipole or ion-dipole interaction had a dominant feature, now the interplay between these two types of dipole-matrix interactions will be considered. We present the results of high frequency dielectric measurements of different concentrations of adenosine monophosphateadenosine-5′- triphosphate aqueous solutions. We observed the Cole-Cole broadening of the main relaxation peak of the solvent in the solutions. Moreover, depending on the nucleotide concentration, we observed both types of dipole-matrix interaction. The 3D trajectory approach (described in detail in Part I) is applied in order to highlight the differences between the two types of interaction.
AB - In this, the third part of our series on the dielectric spectrum symmetrical broadening of water, we consider the nucleotide aqueous solutions. Where in Parts I [E. Levy, J. Chem. Phys. 136, 114502 (2012)10.1063/1.3687914] and II [E. Levy, J. Chem. Phys. 136, 114503 (2012)10.1063/1.3691183], the dipole-dipole or ion-dipole interaction had a dominant feature, now the interplay between these two types of dipole-matrix interactions will be considered. We present the results of high frequency dielectric measurements of different concentrations of adenosine monophosphateadenosine-5′- triphosphate aqueous solutions. We observed the Cole-Cole broadening of the main relaxation peak of the solvent in the solutions. Moreover, depending on the nucleotide concentration, we observed both types of dipole-matrix interaction. The 3D trajectory approach (described in detail in Part I) is applied in order to highlight the differences between the two types of interaction.
UR - http://www.scopus.com/inward/record.url?scp=84870174188&partnerID=8YFLogxK
U2 - 10.1063/1.4766256
DO - 10.1063/1.4766256
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C2 - 23181321
AN - SCOPUS:84870174188
SN - 0021-9606
VL - 137
JO - Journal of Chemical Physics
JF - Journal of Chemical Physics
IS - 19
M1 - 194502
ER -