Literature DB >> 12737570

Study of the lithiated phenylacetonitrile monoanions and dianions formed according to the lithiated base used (LHMDS, LDA, or n-BuLi). 1. Evidence of heterodimer ("Quadac") or dianion formation by vibrational spectroscopy.

Jacques Corset1, Martine Castellà-Ventura, Françoise Froment, Tekla Strzalko, Lya Wartski.   

Abstract

It is evidenced through vibrational spectroscopy that a heterodimer or "Quadac" is formed when an excess of base (LHMDS, LDA, or n-BuLi) is added to PhCH(2)CN in THF, THF-hexane, or THF-toluene solution. The amount of heterodimer increases with the pK(H)(a) of the lithiated base. A dianionic species may be formed through decomposition of this heterodimer if the pK(H)(a) of the base is sufficiently high, as in the case of n-BuLi. With LDA, only a very small amount of dianion is observed, and with LHMDS, no dianion is detected. The predominant dianionic species observed are the linear and bridged separated ion pairs of the dilithiated dianion. The presence of the amine in the medium is of paramount importance. The PhCHCNLi monomer-dimer equilibrium is entropy driven toward the dimer solvated by the amine.

Entities:  

Year:  2003        PMID: 12737570     DOI: 10.1021/jo020492t

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  1 in total

1.  How solvent determines the molecular reactive conformation and the selectivity: Solvation spheres and energy.

Authors:  Joseelyne Hernández-Lima; Karla Ramírez-Gualito; Beatriz Quiroz-García; Ana Luisa Silva-Portillo; Ernesto Carrillo-Nava; Fernando Cortés-Guzmán
Journal:  Front Chem       Date:  2022-09-29       Impact factor: 5.545

  1 in total

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