Published March 5, 1997
| public
Journal Article
Femtosecond Nucleophilic Substitution Reaction Dynamics
- Creators
- Zhong, D.
- Ahmad, S.
- Cheng, P. Y.
- Zewail, A. H.
Abstract
A general class of reactions termed aromatic nucleophilic substitution (S_NAr) is central to organic syntheses, reaction mechanisms, and electron transfer processes. A textbook example is the following reaction which is generally considered as a two-step process, the addition of the nucleophile (a → b) and the elimination to form final products (b → c). However, if the processes of addition and elimination are concerted, the so-called σ-complex (b) becomes a transition state, similar in nature to S_N2 reactions.
Additional Information
© 1997 American Chemical Society. Received November 8, 1996. Publication Date (Web): March 5, 1997. This work was supported by a grant from the National Science Foundation.Additional details
- Eprint ID
- 69877
- Resolver ID
- CaltechAUTHORS:20160824-074504153
- NSF
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