Rate acceleration and subsequent retardation of Diels-Alder reactions in LiClO4-diethyl ether: an experimental investigation

Anil Kumar, ; Pawar, S. S. (2001) Rate acceleration and subsequent retardation of Diels-Alder reactions in LiClO4-diethyl ether: an experimental investigation Journal of Organic Chemistry, 66 (23). pp. 7646-7652. ISSN 0022-3263

Full text not available from this repository.

Official URL: http://pubs.acs.org/doi/abs/10.1021/jo010459r?prev...

Related URL: http://dx.doi.org/10.1021/jo010459r

Abstract

The experimental kinetic data for several Diels-Alder reactions show why a 5 M LiClO4-diethyl ether (LPDE) solution offers maximum enhancement of reaction rates, endo/exo ratios, and yields. These reactions, if carried out in LPDE solutions of concentrations higher than 5 M, show a substantial decrease in these kinetic parameters. This decrease is attributed to the very high viscosity of LPDE solutions near saturation, though this interpretation is not consistent when considered in terms of sizes of the diene and dienophile. The monoetherates, dietherates, and higher other clusters in LPDE solutions and their relationship with the Lewis acid catalysis by Li+ offer a more plausible explanation of both the enhancement and the decrease of the rate of Diels-Alder reactions in this medium.

Item Type:Article
Source:Copyright of this article belongs to American Chemical Society.
ID Code:1596
Deposited On:05 Oct 2010 12:13
Last Modified:12 May 2011 06:14

Repository Staff Only: item control page