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Título : 1D coordination polymer based on copper(II)-containing tetrameric 1,2,3- triazole ligand from click chemistry : magnetic and catalytic properties.
Autor : Teixeira, Leonardo César de Moraes
Souza, Gilmar Pereira de
Fajardo, Humberto Vieira
Luz, Sulusmon Cesar
Álvarez, Eleuterio
Lloret, Francesc
Viana, Renato Márcio Ribeiro
Rojo Marcos, Francisco Javier
Stumpf, Humberto Osório
Figueiredo, Rute Cunha
Correa, Rodrigo de Souza
Palabras clave : Crystal structure
Catalysis
Fecha de publicación : 2019
Citación : TEIXEIRA, L. C. de M. et al. 1D coordination polymer based on copper(II)-containing tetrameric 1,2,3- triazole ligand from click chemistry : magnetic and catalytic properties. Inorganica Chimica Acta, v. 489, p. 93-99, abr. 2019. Disponível em: <https://www.sciencedirect.com/science/article/pii/S0020169318318176>. Acesso em: 7 mar. 2019.
Resumen : A novel tetrameric tetra[O-((1-benzyl-1H-1,2,3-triazol-4-yl)methyl)]-pentaerythritol (TBTP) has been synthesized using click chemistry strategy. TBTP was characterized and used as ligand to form new Cu(II) complexes, forming 1-D coordination polymers. Two square planar complexes were characterized by single-crystal X-ray diffraction, presenting formula [Cu(TBTP)][Cu(NO3)4] (1) and [Cu(TBTP)](NO3)2 (2). In both structures, a cationic 1-D coordination polymer (CP) has been formed. The CP contain a 1:1 Cu(II)/TBTP ratio with four neutral triazole groups coordinating the Cu(II) center, forming a CuN bonds ranging 1.988(2)–2.001(2) Å. The study of the magnetic properties of compounds 1 and 2 pointed to an antiferromagnetic behavior for both compounds, defined by inter- and intra-chain dipolar interactions among their metallic centers. In addition, the complex 1 was found to be an efficient catalyst for selective oxidation of aniline to azobenzene under mild reaction conditions.
URI : http://www.repositorio.ufop.br/handle/123456789/11188
metadata.dc.identifier.uri2: https://www.sciencedirect.com/science/article/pii/S0020169318318176
metadata.dc.identifier.doi: https://doi.org/10.1016/j.ica.2019.02.010
ISSN :  0020-1693
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