Evidence map›Paper›PMID 21303143›Full record

ArticleThe Journal of chemical physics2011

Water dynamics in small reverse micelles in two solvents: two-dimensional infrared vibrational echoes with two-dimensional background subtraction.

Emily E Fenn, Daryl B Wong, M D Fayer

Abstract read
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Article in The Journal of chemical physics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Mechanisms of the viscosity decrease and increase of aqueous CsCl.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Vibrational spectroscopy of water at interfaces.Accounts of chemical research · 2012
    Article
  4. Article
  5. Molecular Dynamics Simulations of Macromolecular Crystals.Wiley interdisciplinary reviews. Computational molecular science
    Article
4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Emily E FennDepartment of Chemistry, Stanford University, Stanford, California 94305, USA.
Daryl B Wong
M D Fayer

Funding

Protein, Enzyme, and Biological Water Dynamics: 2D Vibrational Echo SpectroscopyR01GM061137 · NIGMS · STANFORD UNIVERSITY · PI FAYER, MICHAEL D · 2000 to 2011
$3.1M
NIGMS NIH HHS 2-R01-GM061137-09NIGMS NIH HHS R01 GM061137
6 · The paper itself

Abstract

Water dynamics as reflected by the spectral diffusion of the water hydroxyl stretch were measured in w(0) = 2 (1.7 nm diameter) Aerosol-OT (AOT)/water reverse micelles in carbon tetrachloride and in isooctane solvents using ultrafast 2D IR vibrational echo spectroscopy. Orientational relaxation and population relaxation are observed for w(0) = 2, 4, and 7.5 in both solvents using IR pump-probe measurements. It is found that the pump-probe observables are sensitive to w(0), but not to the solvent. However, initial analysis of the vibrational echo data from the water nanopool in the reverse micelles in the isooctane solvent seems to yield different dynamics than the CCl(4) system in spite of the fact that the spectra, vibrational lifetimes, and orientational relaxation are the same in the two systems. It is found that there are beat patterns in the interferograms with isooctane as the solvent. The beats are observed from a signal generated by the AOT/isooctane system even when there is no water in the system. A beat subtraction data processing procedure does a reasonable job of removing the distortions in the isooctane data, showing that the reverse micelle dynamics are the same within experimental error regardless of whether isooctane or carbon tetrachloride is used as the organic phase. Two time scales are observed in the vibrational echo data, ~1 and ~10 ps. The slower component contains a significant amount of the total inhomogeneous broadening. Physical arguments indicate that there is a much slower component of spectral diffusion that is too slow to observe within the experimental window, which is limited by the OD stretch vibrational lifetime.

Indexed as

Carbon TetrachlorideDioctyl Sulfosuccinic AcidMicellesOctanesSolventsSpectrophotometry, InfraredSurface-Active AgentsWater2,2,4-trimethylpentaneCarbon TetrachlorideDioctyl Sulfosuccinic AcidMicellesOctanesSolventsSurface-Active AgentsWater

Identifiers

PMID21303143
PMCPMC3055695

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.