The influence of fluorination on the dynamics of the F + CH3CH2I reaction

Author:

Gstir Thomas1ORCID,Michaelsen Tim1,Long Bryan A.2,Nacsa András B.3ORCID,Ayasli Atilay1,Swaraj Dasarath1,Zappa Fabio1ORCID,Trummer Florian1ORCID,Ard Shaun G.2ORCID,Shuman Nicholas S.2ORCID,Czakó Gábor3ORCID,Viggiano Albert A.2ORCID,Wester Roland1ORCID

Affiliation:

1. Institut für Ionenphysik und Angewandte Physik, Universität Innsbruck, 6020 Innsbruck, Austria

2. Air Force Research Laboratory, Space Vehicles Directorate, Kirtland Air Force Base, NM 87117, USA

3. MTA-SZTE Lendület Computational Reaction Dynamics Research Group, Interdisciplinary Excellence Centre and Department of Physical Chemistry and Materials Science, Institute of Chemistry, University of Szeged, Rerrich Béla tér 1, Szeged H-6720, Hungary

Abstract

Fluorination at the beta-carbon of ethyl iodide leads to a set of new product channels in the reaction with fluorine anions, which show rich reaction dynamics.

Funder

Air Force Office of Scientific Research

Austrian Science Fund

Nemzeti Kutatási Fejlesztési és Innovációs Hivatal

Nemzeti Kutatási, Fejlesztési és Innovaciós Alap

Magyar Tudományos Akadémia

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Reference48 articles.

1. M. B.Smith and J.March , March's Advanced Organic Chemistry: Reactions, Mechanisms and Structure , John Wiley & Sons , 2007

2. Gas phase nucleophilic substitution

3. Ueber die gegenseitige Umwandlung optischer Antipoden

4. 55. Mechanism of substitution at a saturated carbon atom. Part IV. A discussion of constitutional and solvent effects on the mechanism, kinetics, velocity, and orientation of substitution

5. F. A.Carey and R. J.Sundberg , Nucleophilic substitution , Springer , 2007 , pp. 389–479

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