Utilize este identificador para referenciar este registo: http://hdl.handle.net/10400.21/9478
Título: Solvent-free microwave-assisted peroxidative oxidation of alcohols catalyzed by iron(III)-TEMPO catalytic systems
Autor: Karmakar, Anirban
Martins, Luisa
Guedes Da Silva, M. Fátima C.
Pombeiro, Armando
Palavras-chave: Alcohol oxidation
Mononuclear iron(III) complexes
Microwave-assisted catalysis
Data: Dez-2015
Editora: Springer
Citação: KARMAKAR, Anirban; [et al] – Solvent-free microwave-assisted peroxidative oxidation of alcohols catalyzed by iron(III)-TEMPO catalytic systems. Catalysis Letters. ISSN 1011-372X. Vol. 145, N.º 12 (2015), pp. 2066-2076
Resumo: The iron(III) complexes [H(EtOH)][FeCl2(L)(2)] (1), [H(2)bipy](1/2)[FeCl2(L)(2)].DMF (2) and [FeCl2(L)(2,2'-bipy)] (3) (L = 3-amino-2-pyrazinecarboxylate; H(2)bipy = doubly protonated 4,4'-bipyridine; 2,2'-bipy = 2,2'-bipyridine, DMF = dimethylformamide) have been synthesized and fully characterized by IR, elemental and single-crystal X-ray diffraction analyses, as well as by electrochemical methods. Complexes 1 and 2 have similar mononuclear structures containing different guest molecules (protonated ethanol for 1 and doubly protonated 4,4'-bipyridine for 2) in their lattices, whereas the complex 3 has one 3-amino-2-pyrazinecarboxylate and a 2,2'-bipyridine ligand. They show a high catalytic activity for the low power (10 W) solvent-free microwave assisted peroxidative oxidation of 1-phenylethanol, leading, in the presence of TEMPO, to quantitative yields of acetophenone [TOFs up to 8.1 x 10(3) h(-1), (3)] after 1 h. Moreover, the catalysts are of easy recovery and reused, at least for four consecutive cycles, maintaining 83 % of the initial activity and concomitant rather high selectivity. 3-Amino-2-pyrazinecarboxylic acid is used to synthesize three new iron(III) complexes which act as heterogeneous catalysts for the solvent-free microwave-assisted peroxidative oxidation of 1-phenylethanol.
Peer review: yes
URI: http://hdl.handle.net/10400.21/9478
DOI: 10.1007/s10562-015-1616-2
ISSN: 1011-372X
Versão do Editor: https://link.springer.com/content/pdf/10.1007%2Fs10562-015-1616-2.pdf
Aparece nas colecções:ISEL - Eng. Quim. Biol. - Artigos

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