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Powerful Bispyridinylidene Organic Reducing Agents with Iminophosphorano π-Donor Substituents.
Hanson, Samuel S; Richard, Nicholas A; Dyker, C Adam.
Afiliación
  • Hanson SS; Department of Chemistry, University of New Brunswick, Fredericton, New Brunswick, E3B 5A3 (Canada).
  • Richard NA; Department of Chemistry, University of New Brunswick, Fredericton, New Brunswick, E3B 5A3 (Canada).
  • Dyker CA; Department of Chemistry, University of New Brunswick, Fredericton, New Brunswick, E3B 5A3 (Canada). cadyker@unb.ca.
Chemistry ; 21(22): 8052-5, 2015 May 26.
Article en En | MEDLINE | ID: mdl-25877958
ABSTRACT
Four members of a new family of powerful bispyridinylidene organic reducing agents have been prepared, which exploit iminophosphorano (-N=PR3; R = Ph, Cy) π-donor substituents. Electrochemical studies show exceptionally high oxidation potentials, ranging from 1.30 to 1.51 V versus SCE. These new reductants were shown to effectively convert 1-bromonaphthalene to naphthalene under mild reaction conditions. From the redox potentials, substituent constants (σp(+)) for the iminophosphorano groups Ph3P=N- (-1.82) and Cy3P=N- (-2.21) were determined, demonstrating their superior π-donating properties compared to traditional amino substituents.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2015 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2015 Tipo del documento: Article