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Visible Light-Gated Organocatalysis Using a RuII -Photocage.
González-Delgado, José A; Romero, Miguel A; Boscá, Francisco; Arteaga, Jesús F; Pischel, Uwe.
Afiliación
  • González-Delgado JA; CIQSO-Center for Research in Sustainable Chemistry and, Department of Chemistry, University of Huelva, Campus de El Carmen s/n, 21071, Huelva, Spain.
  • Romero MA; CIQSO-Center for Research in Sustainable Chemistry and, Department of Chemistry, University of Huelva, Campus de El Carmen s/n, 21071, Huelva, Spain.
  • Boscá F; Instituto Universitario Mixto de Tecnología Química (ITQ-UPV), Universitat Politècnica de València, Av. de los Naranjos s/n, 46022, Valencia, Spain.
  • Arteaga JF; CIQSO-Center for Research in Sustainable Chemistry and, Department of Chemistry, University of Huelva, Campus de El Carmen s/n, 21071, Huelva, Spain.
  • Pischel U; CIQSO-Center for Research in Sustainable Chemistry and, Department of Chemistry, University of Huelva, Campus de El Carmen s/n, 21071, Huelva, Spain.
Chemistry ; 26(62): 14229-14235, 2020 Nov 06.
Article en En | MEDLINE | ID: mdl-32449554
ABSTRACT
The light-gated organocatalysis via the release of 4-N,N-dimethylaminopyridine (DMAP) by irradiation of the [Ru(bpy)2 (DMAP)2 ]2+ complex with visible light was investigated. As model reaction the acetylation of benzyl alcohols with acetic anhydride was chosen. The pre-catalyst releases one DMAP molecule on irradiation at wavelengths longer than 455 nm. The photochemical process was characterized by steady-state irradiation and ultrafast transient absorption spectroscopy. The latter enabled the observation of the 3 MLCT state and the spectral features of the penta-coordinated intermediate [Ru(bpy)2 (DMAP)]2+ . The released DMAP catalyzes the acetylation of a wide range of benzyl alcohols with chemical yields of up to 99 %. Control experiments revealed unequivocally that it is the released DMAP which takes the role of the catalyst.
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2020 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2020 Tipo del documento: Article País de afiliación: España