Skip to content Skip to navigation
University of Warwick
  • Study
  • |
  • Research
  • |
  • Business
  • |
  • Alumni
  • |
  • News
  • |
  • About

University of Warwick
Publications service & WRAP

Highlight your research

  • WRAP
    • Home
    • Search WRAP
    • Browse by Warwick Author
    • Browse WRAP by Year
    • Browse WRAP by Subject
    • Browse WRAP by Department
    • Browse WRAP by Funder
    • Browse Theses by Department
  • Publications Service
    • Home
    • Search Publications Service
    • Browse by Warwick Author
    • Browse Publications service by Year
    • Browse Publications service by Subject
    • Browse Publications service by Department
    • Browse Publications service by Funder
  • Statistics
  • Help & Advice
University of Warwick

The Library

  • Login

Solvation structure around aqueous alcohols

Tools
- Tools
+ Tools

UNSPECIFIED (1999) Solvation structure around aqueous alcohols. JOURNAL OF PHYSICAL CHEMISTRY B, 103 (36). pp. 7695-7703. ISSN 1089-5647

Full text not available from this repository.

Abstract

Molecular dynamics simulations have been used to characterize the structure of water around n-alcohols (methanol to butanol) in dilute aqueous solution. A number of different analyses have been used to examine the extent to which the alcohol modifies the behavior of neighboring water molecules. These include radial distribution functions, specific order parameters designed to probe for ice- and clathrate-like local structures, and velocity and orientational time correlation functions. The static structure of water around the hydrophobic end of the alcohol was found to be essentially the same as that found in bulk water; in particular, there was no evidence of clathrate-like cages around the hydrophobic end of the alcohol. Some enhancement of the water structure was found in the vicinity of the alcohol hydroxyl group, with the hydrogen bonding network being closer to tetrahedral in the solvation shell than in bulk water; however, this enhancement was unaffected by the length of the associated hydrophobic chain. In contrast, the dynamic behavior of water was considerably modified near all parts of the alcohols, with both translational and rotational motion being slower for water in the solvation shell than in the bulk. Only in the case of water solvating the hydroxyl group was the dynamical behavior found to vary between the different alcohols, with the dynamics getting slower along the series from methanol to n-butanol. This was found to be largely due to inertial effects and not due to variations in the strength of the hydrogen bonding networks.

Item Type: Journal Article
Subjects: Q Science > QD Chemistry
Journal or Publication Title: JOURNAL OF PHYSICAL CHEMISTRY B
Publisher: AMER CHEMICAL SOC
ISSN: 1089-5647
Date: 9 September 1999
Volume: 103
Number: 36
Number of Pages: 9
Page Range: pp. 7695-7703
Publication Status: Published
URI: http://wrap.warwick.ac.uk/id/eprint/14187

Data sourced from Thomson Reuters' Web of Knowledge

Request changes to a record

Actions (login required)

View Item View Item
twitter

Email us: publications@warwick.ac.uk
Contact Details
About Us