Issue 3, 1979

Linear solvation energy relationships. Part 3. Some reinterpretations of solvent effects based on correlations with solvent π* and α values

Abstract

Solvent polarity and hydrogen bonding effects on a number of physical and chemical properties and reaction parameters are unravelled and rationalized by means of the solvatochromic comparison method and equations of the form XYZ=XYZ0+sπ*+aα, where π* is a measure of solvent polarity and α a measure of solvent hydrogen bond donor acidity. XYZ's considered include ET values for eight electronic spectral transitions, two sets of nitrogen hyperfine splitting constants, a set of fluorescence lifetimes, logarithms of rate constants for four nucleophilic substitution reactions, and the ‘electrophilicity parameter,’E, of Koppel and Palm.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1979, 349-356

Linear solvation energy relationships. Part 3. Some reinterpretations of solvent effects based on correlations with solvent π* and α values

M. J. Kamlet and R. W. Taft, J. Chem. Soc., Perkin Trans. 2, 1979, 349 DOI: 10.1039/P29790000349

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