Hydration of tetraphenylphosphonium and tetraphenylborate ions by dielectric relaxation spectroscopy

Wachter, Wolfgang and Buchner, Richard and Hefter, Glenn (2006) Hydration of tetraphenylphosphonium and tetraphenylborate ions by dielectric relaxation spectroscopy. JOURNAL OF PHYSICAL CHEMISTRY B, 110 (10). pp. 5147-5154. ISSN 1520-6106,

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Abstract

A systematic study of the dielectric relaxation spectra of aqueous solutions of NaBPh4 and Ph4PCl has been made at solute concentrations of 0.02 <= c/M <= 0.82 and 0.20, respectively, and over a wide range of frequencies (0.2 <= nu/GHz <= 89) at 25 degrees C. The spectra were best described by a superposition of four Debye processes, consisting of a very small ion-pair contribution with an average relaxation time of about 300 ps, a "slow" water relaxation at 17 ps, and two bulk-water relaxations at 8 ps and 0.25 ps, respectively. The slow-water process has been assigned to the presence of a sheath of water molecules surrounding BPh4- and Ph4P+, whose structure has been enhanced by its proximity to the bulky hydrophobic phenyl rings. A structure-making effect on the remaining solvent water can also be observed at low concentrations. More importantly, BPh4- and Ph4P+ show almost identical hydration characteristics, which provides indirect support for the use of the tetraphenylphosphonium tetraphenylborate reference electrolyte assumption in deriving single-ion thermodynamic properties.

Item Type: Article
Uncontrolled Keywords: AQUEOUS-ELECTROLYTE SOLUTIONS; TEMPERATURE-DEPENDENCE; HEAT-CAPACITIES; SODIUM TETRAPHENYLBORATE; HYDROPHOBIC HYDRATION; SOLVENT RELAXATION; ORGANIC SOLVENTS; WATER-STRUCTURE; B-COEFFICIENTS; LIQUID WATER;
Subjects: 500 Science > 540 Chemistry & allied sciences
Divisions: Chemistry and Pharmacy > Institut für Physikalische und Theoretische Chemie > Chair of Chemistry VI - Physical Chemistry (Solution Chemistry) > PD Dr. Richard Buchner
Depositing User: Dr. Gernot Deinzer
Date Deposited: 17 Feb 2021 12:39
Last Modified: 17 Feb 2021 12:39
URI: https://pred.uni-regensburg.de/id/eprint/34784

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