Issue 18, 1970

Steric effects on the proton transfer rates of formic acid solutions of methylamines

Abstract

Deprotonation of monomethylammonium ion in formic acid involves exclusively the formate anion as the reacting base, in contrast with di- and tri-methyl-amine solutions.

Article information

Article type
Paper

J. Chem. Soc. D, 1970, 1187-1188

Steric effects on the proton transfer rates of formic acid solutions of methylamines

J. J. Delpuech, J. Ducom and V. Michon, J. Chem. Soc. D, 1970, 1187 DOI: 10.1039/C29700001187

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