Utilize este identificador para referenciar este registo: http://hdl.handle.net/10400.21/9081
Título: Peroxidative oxidation of alkanes and alcohols under mild conditions by Di- and tetranuclear copper (II) complexes of Bis (2-Hydroxybenzylidene) isophthalohydrazide
Autor: Sutradhar, Manas
Alegria, Elisabete C. B. A.
Silva, M. Fátima C. Guedes da
Liu, Cai-Ming
Pombeiro, Armando J. L.
Palavras-chave: Cu (II) complexes
Microwave assisted oxidation of alcohols
Oxidation of alkanes
Solvent free process
Magnetism
Data: 19-Out-2018
Editora: MDPI
Citação: SUTRADHAR, Manas; [et al] – Peroxidative oxidation of alkanes and alcohols under mild conditions by Di- and tetranuclear copper (II) complexes of Bis (2-Hydroxybenzylidene) isophthalohydrazide. Molecules. ISSN 1420-3049. Vol. 23, N.º 10 (2018), pp. 1-18
Resumo: Bis(2-hydroxybenzylidene)isophthalohydrazide (H4L) has been used to synthesize the dinuclear [Cu2(1_NO2:2_N0O02-H2L)(NO3)2(H2O)2] (1) and the tetranuclear [Cu4(_-1_NO2:2_N0O2-H2L)2(_-NO3)2(H2O)4]_2C2H5OH (2) complexes. The solvent plays an important role in determining the ligand behaviour in the syntheses of the complexes. An ethanol-acetonitrile mixture of solventes favours partials enolization in the case of 2. Both complexes have been characterized by elemental analysis, infrared radiation (IR), single crystal X-ray crystallography and electrochemical methods. The variable temperature magnetic susceptibility measurements of 2 show strong antiferromagnetic coupling between the central nitrato-bridged Cu (II) ions. The catalytic activity of both 1 and 2 has been screened toward the solvent-free microwave-assisted oxidation of alcohols and the peroxidative oxidation of alkanes under mild conditions. Complex 1 exhibits the highest activity for both oxidation reactions, leading selectively to a maximum product yield of 99% (for the 1-phenylethanol oxidation after 1 h without any additive) and 13% (for the cyclohexane oxidation to cyclohexyl hydroperoxide, cyclohexanol and cyclohexanone after 3 h).
Peer review: yes
URI: http://hdl.handle.net/10400.21/9081
DOI: 10.3390/molecules23102699
ISSN: 1420-3049
Aparece nas colecções:ISEL - Eng. Quim. Biol. - Artigos

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