Copper(II) complexes of embelin and 2-aminobenzimidazole encapsulated in zeolite Y-potential as catalysts

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Copper(II) complexes of embelin and 2-aminobenzimidazole encapsulated in zeolite Y-potential as catalysts

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dc.contributor.author Mohammed Yusuff, K K
dc.contributor.author Rani, Abraham
dc.date.accessioned 2010-04-26T04:30:16Z
dc.date.available 2010-04-26T04:30:16Z
dc.date.issued 2002-12-02
dc.identifier.citation Applied Chemistry,Cochin University of Science and Technology en_US
dc.identifier.issn DOI:10.1016/S1381-1169(02)00687-8
dc.identifier.other www.sciencedirect.com
dc.identifier.uri http://dyuthi.cusat.ac.in/purl/1653
dc.description.abstract Copper(II) complexes of two biologically important ligands, viz., embelin (2,5-dihydroxy-3-undecyl-2,5-cyclohexadien 1,4-dione) and 2-aminobenzimidazole were entrapped in the cages of zeolite Y by the flexible ligand method. The capability of these compounds in catalyzing the reduction of oxygen (industrially known as deoxo reaction) was explored and the results indicate an enhancement of the catalytic properties from that of the simple copper ion exchanged zeolite. These point to the ability of the ligands in enhancing the oxygen binding capability of the metal ion. Elemental analyses, Fourier transform infrared (FTIR), diffuse reflectance and EPR spectral studies, magnetic susceptibility measurements, TG, surface area analyses and powder X-ray diffraction studies were used in understanding the presence, composition and structure of the complexes inside the cages. The study also reveals the increased thermal and mechanical stability of the complexes as a result of encapsulation. en_US
dc.language.iso en en_US
dc.publisher Elsevier,Journal of Molecular Catalysis A: Chemical 198 (2003) 175–183 en_US
dc.subject Zeolite encapsulation en_US
dc.subject Oxygen reduction en_US
dc.subject Deoxo en_US
dc.subject Embelin en_US
dc.subject 2-Aminobenzimidazole en_US
dc.title Copper(II) complexes of embelin and 2-aminobenzimidazole encapsulated in zeolite Y-potential as catalysts en_US
dc.type Working Paper en_US


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