Van Bochove, M.A., Swart, M. and Bickelhaupt, F.M. (2006) Nucleophilic Substitution at Phosphorus (SN2@P): Disappearance and Reappearance of Reaction Barriers. Journal of the American Chemical Society, 128, 10738-10744.
https://doi.org/10.1021/ja0606529

has been cited by the following article:

• TITLE: One-Electron-Addition to Pentavalent Phosphorus with the Phosphorus-Chlorine Bond as Acceptor Introducing a Fundamental Distinction in Substitution Mechanism between SN2(P) and SN2(C)

  AUTHORS: Henk M. Buck

  KEYWORDS: Pentavalent Phosphorus and Carbon Compounds, σ*-Electron-Addition, Single-Crystal Electron Spin Resonance (ESR), Model and Ab Initio Calculations, Differences in SN2(C) vs. SN2(P) Mechanism

  JOURNAL NAME: Open Journal of Physical Chemistry, Vol.9 No.3, August 30, 2019

  ABSTRACT: An electron-addition, under single-crystal conditions, to pentavalent phosphorus compounds as Cl-P (=O, S) Y, Z with the P-Cl bond as electron-accepting group, is selected as an additional model for SN2(P) like reactions. It is demonstrated that the geometric information stored in the tetrahedral configuration (substrate) can be transmitted in the corresponding trigonal bipyramidal (TBP) state for nucleophilic substitution. In this article, we focus on these specific mechanistic aspects of carbon and phosphorus. We consider our study as a contribution to the significance of these (bio)chemical intermediates.