Origin of the Microsolvation Effect on the Central Barriers of S<sub>N</sub>2 Reactions-Reference-Cited by-同舟云学术

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Origin of the Microsolvation Effect on the Central Barriers of S_N2 Reactions

Published:2022-07-02 Issue:27 Volume:126 Page:4342-4348
ISSN:1089-5639
Container-title:The Journal of Physical Chemistry A
language:en
Short-container-title:J. Phys. Chem. A

Author:

Yu Feng¹^ORCID

Affiliation:

1. Department of Physics, School of Freshmen, Xi’an Technological University, No. 4 Jinhua North Road, Xi’an, Shaanxi 710032, China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jpca.2c01677

Reference108 articles.

1. Fifty years of nucleophilic substitution in the gas phase

2. Uggerud, E. Advances in Physical Organic Chemistry; Williams, I. H., Williams, N. H., Eds. Academic Press: New York, 2017; Vol. 51, pp 1–57.

3. Nucleophilic Substitution (SN 2): Dependence on Nucleophile, Leaving Group, Central Atom, Substituents, and Solvent

4. Gas-Phase Ionic Reactions: Dynamics and Mechanism of Nucleophilic Displacements

5. Gas phase nucleophilic substitution

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1. Solvent-induced dual nucleophiles and the α-effect in the S_N2 versus E2 competition;Physical Chemistry Chemical Physics;2024

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