Influence of the channel size of isostructural 3d–4f MOFs on the catalytic aerobic oxidation of cycloalkenes. (25th June 2019)

• Record Type: Journal Article
• Authors: Cancino, Patricio; Santibañez, Luis; Stevens, Christian; Fuentealba, Pablo; Audebrand, Nathalie; Aravena, Daniel; Torres, Julia; Martinez, Sebastian; Kremer, Carlos; Spodine, Evgenia
• Is Part Of: New journal of chemistry. Volume 43:Number 28(2019)
• Page Start: 11057
• Page End: 11064
• Publication Date: 2019-06-25
• Subjects: Chemistry -- Periodicals; Chimie -- Périodiques; 540
• DOI: 10.1039/c9nj02091h
• Languages: English
• ISSNs: 1144-0546

Abstract

Abstract : The present work reports a new group of heterogeneous catalysts with a 3D structure, CuLnIDA, {[Cu3 Ln2 (IDA)6 ]·8H2 O} (Ln: La III, Gd III or Yb III ), with an organic linker (H2 IDA: iminodiacetic acid). Abstract : The present work reports a new group of heterogeneous catalysts with a 3D structure, CuLnIDA, {[Cu3 Ln2 (IDA)6 ]·8H2 O} (Ln: La III, Gd III or Yb III ), with an organic linker (H2 IDA: iminodiacetic acid). Different sets of O2 pressure and time were used in order to obtain the optimal reaction conditions at 75 °C. The reaction was found to depend on the [aldehyde]/[substrate] ratio. The best results, with a conversion of 73% for CuLaIDA as the catalyst, were obtained for the smallest ratio of 0.2. Finally, the importance of the pore size was analysed by comparing the catalytic activity of the as formed catalyst with that of the thermally activated one. The conversion increased ca. 26–35% for the different catalysts when they were previously activated. In addition, the selectivity increased towards cyclohexenone. The use of molecular oxygen as the oxidizing agent in a system where an auxiliary solvent is not used, as the cyclohexene substrate and products play the role of a solvent, permitted us to generate a more friendly environmental system for the oxidation of cycloalkenes under mild conditions.