Issue 15, 1991

Enthalpies of transfer of some non-electrolytes from acetonitrile to acetonitrile–methanol mixtures

Abstract

The enthalpies of transfer of water, propan-1-ol, 2-methylpropan-2-ol, octan-1-ol, formamide, N-methyl-formamide, N,N-dimethylformamide, dimethyl sulphoxide and propylene carbonate from acetonitrile to methanol and acetonitrile–methanol mixtures are reported and analysed in terms of solvation theory. The analyses show that all of the solutes, except propylene carbonate, interact more strongly with methanol than acetonitrile, and are preferentially solvated by methanol in the mixed solvents. It is also found that the extent to which the solutes disrupt solvent–solvent bonding is greatest for the amides and dimethyl sulphoxide, which act only as hydrogen-bond acceptors, and is relatively insensitive to the size of the alkyl groups on the alcohols.

Article information

Article type
Paper

J. Chem. Soc., Faraday Trans., 1991,87, 2443-2446

Enthalpies of transfer of some non-electrolytes from acetonitrile to acetonitrile–methanol mixtures

A. Costigan, D. Feakins, I. McStravick, C. O'Duinn, J. Ryan and W. E. Waghorne, J. Chem. Soc., Faraday Trans., 1991, 87, 2443 DOI: 10.1039/FT9918702443

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements