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1D Copper(II)-Aroylhydrazone Coordination Polymers: Magnetic Properties and Microwave Assisted Oxidation of a Secondary Alcohol

The 1D Cu(II) coordination polymers [Cu(3)(L(1))(NO(3))(4)(H(2)O)(2)](n) (1) and [Cu(2)(H(2)L(2))(NO(3))(H(2)O)(2)](n)(NO(3))(n) (2) have been synthesized using the aroylhyrazone Schiff bases N'(1),N'(2)-bis(pyridin-2-ylmethylene)oxalohydrazide (H(2)L(1)) and N'(1),N'(3)-bis(2-hy...

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Detalles Bibliográficos
Autores principales: Sutradhar, Manas, Alegria, Elisabete C. B. A., Barman, Tannistha Roy, Guedes da Silva, M. Fátima C., Liu, Cai-Ming, Pombeiro, Armando J. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7069101/
https://www.ncbi.nlm.nih.gov/pubmed/32211380
http://dx.doi.org/10.3389/fchem.2020.00157
Descripción
Sumario:The 1D Cu(II) coordination polymers [Cu(3)(L(1))(NO(3))(4)(H(2)O)(2)](n) (1) and [Cu(2)(H(2)L(2))(NO(3))(H(2)O)(2)](n)(NO(3))(n) (2) have been synthesized using the aroylhyrazone Schiff bases N'(1),N'(2)-bis(pyridin-2-ylmethylene)oxalohydrazide (H(2)L(1)) and N'(1),N'(3)-bis(2-hydroxybenzylidene)malonohydrazide (H(4)L(2)), respectively. They have been characterized by elemental analysis, infrared (IR) spectroscopy, UV-Vis spectroscopy, electrospray ionization mass spectrometry (ESI-MS), single crystal X-ray diffraction and variable temperature magnetic susceptibility measurements (for 2). The ligand (L(1))(2−) coordinates in the iminol form in 1, whereas the amide coordination is observed for (H(2)L(2))(2−) in 2. Either the ligand bridge or the nitrate bridge in 2 mediates weak antiferromagnetic coupling. The catalytic performance of 1 and 2 has been investigated toward the solvent-free microwave-assisted oxidation of a secondary alcohol (1-phenylethanol used as model substrate). At 120°C and in the presence of the nitroxyl radical 2,2,6,6-tetramethylpiperydil-1-oxyl (TEMPO), the complete conversion of 1-phenylethanol into acetophenone occurs with TOFs up to 1,200 h(−1).