Not all third-row elements experience the fluorine gauche effect: β-fluorinated organophosphorus compounds

Author:

Andrade Laize A. F.1234,Freitas Matheus P.1234ORCID

Affiliation:

1. Department of Chemistry

2. Federal University of Lavras

3. Lavras

4. Brazil

Abstract

Conformational analyses of β-fluorinated organophosphorus compounds were theoretically carried out to probe the role of a possible fluorine–phosphorus gauche effect in conformer stabilization, specifically using a phosphine, a phosphine oxide, phosphinic and phosphonic acids, and the corresponding anions as model compounds.

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Fundação de Amparo à Pesquisa do Estado de Minas Gerais

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Reference33 articles.

1. D. Voet , J. G.Voet and C. W.Pratt, Fundamentals of Biochemistry, John Wiley & Sons, Hoboken, 1999

2. K. D. Racke , in Organophosphates: Chemistry, Fate, and Effects, ed. J. E. Chambers and P. E. Levi, Academic Press, San Diego, 1992, ch. 3, pp. 47–73

3. Anomeric effect plays a major role in the conformational isomerism of fluorinated pnictogen compounds

4. Conformational Analysis in Heterocyclic Systems: Recent Results and Applications

5. Origin of Fluorine/Sulfur Gauche Effect of β-Fluorinated Thiol, Sulfoxide, Sulfone, and Thionium Ion

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