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Reduction of Dinitrogen to Ammonia Catalyzed by Molybdenum Diamido Complexes.
Wickramasinghe, Lasantha A; Ogawa, Takaya; Schrock, Richard R; Müller, Peter.
Afiliación
  • Wickramasinghe LA; Department of Chemistry 6-331, Massachusetts Institute of Technology , Cambridge, Massachusetts 02139, United States.
  • Ogawa T; Department of Chemistry 6-331, Massachusetts Institute of Technology , Cambridge, Massachusetts 02139, United States.
  • Schrock RR; Department of Chemistry 6-331, Massachusetts Institute of Technology , Cambridge, Massachusetts 02139, United States.
  • Müller P; Department of Chemistry 6-331, Massachusetts Institute of Technology , Cambridge, Massachusetts 02139, United States.
J Am Chem Soc ; 139(27): 9132-9135, 2017 07 12.
Article en En | MEDLINE | ID: mdl-28640615
ABSTRACT
[Ar2N3]Mo(N)(O-t-Bu), which contains the conformationally rigid pyridine-based diamido ligand, [2,6-(ArNCH2)2NC5H3]2- (Ar = 2,6-diisopropylphenyl), can be prepared from H2[Ar2N3], butyllithium, and (t-BuO)3Mo(N). [Ar2N3]Mo(N)(O-t-Bu) serves as a catalyst or precursor for the catalytic reduction of molecular nitrogen to ammonia in diethyl ether between -78 and 22 °C in a batchwise manner with CoCp*2 as the electron source and Ph2NH2OTf as the proton source. Up to ∼10 equiv of ammonia can be formed per Mo with a maximum efficiency in electrons of ∼43%.

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos