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C-H and C-F Bond Activation Reactions of Fluorinated Propenes at Rhodium: Distinctive Reactivity of the Refrigerant HFO-1234yf.
Talavera, Maria; von Hahmann, Cortney N; Müller, Robert; Ahrens, Mike; Kaupp, Martin; Braun, Thomas.
Afiliación
  • Talavera M; Department of Chemistry, Humboldt Universität zu Berlin, Brook-Taylor-Strasse 2, 12489, Berlin, Germany.
  • von Hahmann CN; Department of Chemistry, Humboldt Universität zu Berlin, Brook-Taylor-Strasse 2, 12489, Berlin, Germany.
  • Müller R; Institut für Chemie, Theoretische Chemie/Quantenchemie, Sekr. C7, Technische Universität Berlin, Strasse des 17. Juni 135, 10623, Berlin, Germany.
  • Ahrens M; Department of Chemistry, Humboldt Universität zu Berlin, Brook-Taylor-Strasse 2, 12489, Berlin, Germany.
  • Kaupp M; Institut für Chemie, Theoretische Chemie/Quantenchemie, Sekr. C7, Technische Universität Berlin, Strasse des 17. Juni 135, 10623, Berlin, Germany.
  • Braun T; Department of Chemistry, Humboldt Universität zu Berlin, Brook-Taylor-Strasse 2, 12489, Berlin, Germany.
Angew Chem Int Ed Engl ; 58(31): 10688-10692, 2019 Jul 29.
Article en En | MEDLINE | ID: mdl-31102565
ABSTRACT
The reaction of [Rh(H)(PEt3 )3 ] (1) with the refrigerant HFO-1234yf (2,3,3,3-tetrafluoropropene) affords an efficient route to obtain [Rh(F)(PEt3 )3 ] (3) by C-F bond activation. Catalytic hydrodefluorinations were achieved in the presence of the silane HSiPh3 . In the presence of a fluorosilane, 3 provides a C-H bond activation followed by a 1,2-fluorine shift to produce [Rh{(E)-C(CF3 )=CHF}(PEt3 )3 ] (4). Similar rearrangements of HFO-1234yf were observed at [Rh(E)(PEt3 )3 ] [E=Bpin (6), C7 D7 (8), Me (9)]. The ability to favor C-H bond activation using 3 and fluorosilane is also demonstrated with 3,3,3-trifluoropropene. Studies are supported by DFT calculations.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2019 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2019 Tipo del documento: Article País de afiliación: Alemania