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Journal ArticleDOI

Vibrational energy relaxation of the cyanide ion in aqueous solution

E. J. Heilweil, +3 more
- 01 Jun 1982 - 
- Vol. 76, Iss: 11, pp 5632-5634
TLDR
In this article, the authors reported the vibration energy relaxation (T1) of the CN− ion in saturated H2O/D2O and dilute H 2O solutions at room temperature.
Abstract
Vibrational energy relaxation (T1) of the CN− ion is reported for NaCN in saturated H2O/D2O and dilute H2O solutions at room temperature. Time domain measurements of the v = 1, 2080 cm−1 vibration shown T1 is on the order of a few picoseconds. The relaxation time increases with dilution and is apparently sensitive to cation (Na+,K+) and local solution structure.

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Citations
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Journal ArticleDOI

Structural dynamics of aqueous salt solutions.

TL;DR: Structural Dynamics of Ionic Hydrations Shells: A Beginner's Guide to the Physics of Shells 1457-1457 2.1.
Journal ArticleDOI

Applications of 2D IR spectroscopy to peptides, proteins, and hydrogen-bond dynamics.

TL;DR: Recent experiments on the hydrogen-bond dynamics of small ions, amide-I modes, nitrile probes, peptides, reverse transcriptase inhibitors, and amyloid fibrils are described.
Journal ArticleDOI

Vibrational energy relaxation of the cyanide ion in water

TL;DR: In this paper, the vibrational relaxation time of the cyanide ion in H2O and in D2O was measured by IR-pump-IR-probe experiments, where the isotopic composition of the ion was varied in order vary the oscillation frequency of the CN− vibrational mode.
Journal ArticleDOI

Vibrational relaxation of a dipolar molecule in water

TL;DR: In this article, the vibrational energy relaxation of a model methyl chloride molecule in water is studied through equilibrium and nonequilibrium molecular dynamics simulations, and an analysis of this friction is used to test the isolated binary interaction (IBI) approximation.
Journal ArticleDOI

Nonlinear spectroscopy and picosecond transient grating study of colloidal gold

TL;DR: In this paper, an analysis of the observed dispersion has revealed that the T1 and T2 lifetimes for the plasmon excitation are extremely rapid (2 ps).
References
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Journal ArticleDOI

Vibrational dynamics of liquids and solids investigated by picosecond light pulses

TL;DR: In this article, a detailed theoretical treatment of different excitation and probing processes are outlined and a variety of results are presented and discussed, including the population lifetime of known vibrational modes and evidence for inter-and intra-molecular interactions.
Journal ArticleDOI

Dephasing processes of molecular vibrations in liquids

TL;DR: In this article, a model based on semiclassical collision theory is presented to describe the dephasing of vibrationally excited molecules in a liquid, and it is shown that fluctuations of the vibrational frequencies which are caused by the intermolecular interaction, lead to phase relaxation of a coherently excited state.
Journal ArticleDOI

Raman Study of Liquids. I. Theory of the Raman Spectra of Diatomic Molecules in Inert Solutions

TL;DR: In this paper, a stochastic-type theory related to similar theories of infrared and NMR spectra was proposed to explain the Raman spectra of inert solutions of diatomic molecules.

Liquid state chemical physics

TL;DR: In this article, a liquid state chemical physics can be used to solve the problem of where to get the ideas for a novel, which can be one of the right sources to develop a writing skill.
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