Articles producció científica> Química Física i Inorgànica

Iron(III) versatile catalysts for cycloaddition of CO2 to epoxides and epoxidation of alkenes

  • Dades identificatives

    Identificador: PC:2702
    Autors:
    Cuesta-Aluja, L.Masdeu-Bultó, A.M.
    Resum:
    Fe(III) complexes with tridentate pyridine-imine-phenolato ligands differing in the chain length between the imine and pyridine groups (2-methylpyridine L1 and 2-ethylpyridine L2) have been synthesized. New complex [Fe(L2)2]ClO4 (2) was characterized by X-ray diffraction and spectroscopic techniques. [Fe(L1)2]ClO4 (1) and 2 form active catalysts for the cycloaddition of CO2 to epoxides and for the epoxidation of alkenes. Catalytic systems with the more flexible skeleton (2) in combination with tetrabutylammonium bromide (TBAB) were more active than 1/TBAB in the cycloaddition of CO2 to epoxides. TOFs up to 900 h−1 for the selective synthesis of styrene carbonate and 3640 h−1 for the synthesis of glycidol carbonate were obtained using 2/TBAB at low catalyst loadings (0.025 mol %). Additionally, 2 was also active in the epoxidation of styrene derivatives such as trans-stilbene (conversion 88 %) and trans-β-methylstyrene (conversion 100 %) using tert-butylhydroperoxide as oxidant at 60 ºC in acetonitrile. Epoxidation of styrene and cyclohexene proceed at low conversions.
  • Altres:

    Autor segons l'article: Cuesta-Aluja, L.; Masdeu-Bultó, A.M.
    Departament: Química Física i Inorgànica
    Autor/s de la URV: CUESTA ALUJA, LAIA; MASDEU BULTÓ, ANNA MARIA
    Paraules clau: Fe(III) catalysis
    Resum: Fe(III) complexes with tridentate pyridine-imine-phenolato ligands differing in the chain length between the imine and pyridine groups (2-methylpyridine L1 and 2-ethylpyridine L2) have been synthesized. New complex [Fe(L2)2]ClO4 (2) was characterized by X-ray diffraction and spectroscopic techniques. [Fe(L1)2]ClO4 (1) and 2 form active catalysts for the cycloaddition of CO2 to epoxides and for the epoxidation of alkenes. Catalytic systems with the more flexible skeleton (2) in combination with tetrabutylammonium bromide (TBAB) were more active than 1/TBAB in the cycloaddition of CO2 to epoxides. TOFs up to 900 h−1 for the selective synthesis of styrene carbonate and 3640 h−1 for the synthesis of glycidol carbonate were obtained using 2/TBAB at low catalyst loadings (0.025 mol %). Additionally, 2 was also active in the epoxidation of styrene derivatives such as trans-stilbene (conversion 88 %) and trans-β-methylstyrene (conversion 100 %) using tert-butylhydroperoxide as oxidant at 60 ºC in acetonitrile. Epoxidation of styrene and cyclohexene proceed at low conversions.
    Grup de recerca: Organometàl.lics i Catàlisi Homogènia
    Àrees temàtiques: Chemistry Química Química
    Accès a la llicència d'ús: https://creativecommons.org/licenses/by/3.0/es/
    ISSN: 2365-6549
    Identificador de l'autor: ;
    Data d'alta del registre: 2017-03-22
    Pàgina final: 2070
    Volum de revista: 1
    Versió de l'article dipositat: info:eu-repo/semantics/acceptedVersion
    Enllaç font original: http://onlinelibrary.wiley.com/doi/10.1002/slct.201600488/abstract
    URL Document de llicència: https://repositori.urv.cat/ca/proteccio-de-dades/
    DOI de l'article: 10.1002/slct.201600488
    Entitat: Universitat Rovira i Virgili
    Any de publicació de la revista: 2016
    Pàgina inicial: 2065
    Tipus de publicació: Article Artículo Article
  • Paraules clau:

    Catalitzadors
    Anhídrid carbònic
    Fe(III) catalysis
    Chemistry
    Química
    Química
    2365-6549
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