Electrostatic Switching between S N 1 and S N 2 Pathways

Li Juan Yu, Michelle L. Coote

Research output: Contribution to journalArticlepeer-review

19 Citations (Scopus)

Abstract

A test set 264 nucleophilic substitution reactions was studied via accurate quantum chemical reactions to establish the relative preferences for S N 1 versus S N 2 mechanisms. In low polar solvents, reactions involving anionic nucleophiles and leaving groups favored S N 2 pathways. In contrast, S N 1 is preferred for those reactions involving neutral nucleophiles and leaving groups except where the carbocation intermediates are exceptionally unstable. For neutral nucleophiles and anionic leaving groups, S N 2 is generally preferred over S N 1 except for exceptionally stable carbocation intermediates. On the basis of these studies, candidate reactions for which distinct S N 1 or S N 2 preferences could be reversed by electric fields were selected. As proof of concept, the S N 1/S N 2 preferences for the reaction of tBu-triflate with pyridine (S N 2 to S N 1) and with piperidine (S N 1 to S N 2) were switched by both charged functional groups and point charges (i.e., electric fields) along the reaction axis, with a positive charge on the nucleophile side favoring S N 1 and a negative charge favoring S N 2 for these reactions.

Original languageEnglish
Pages (from-to)582-589
Number of pages8
JournalJournal of Physical Chemistry A
Volume123
Issue number2
DOIs
Publication statusPublished - 17 Jan 2019
Externally publishedYes

Keywords

  • Electric fields
  • Free energy
  • Substitution reactions
  • Chemical reactions
  • Functional groups

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