Preparation, magnetic and EPR spectral studies of copper(II) complexes of an anticancer drug analogue

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Preparation, magnetic and EPR spectral studies of copper(II) complexes of an anticancer drug analogue

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dc.contributor.author Prathapachandra Kurup, M R
dc.contributor.author Alex, Punnoose
dc.contributor.author Manoj, E
dc.date.accessioned 2014-07-14T06:56:41Z
dc.date.available 2014-07-14T06:56:41Z
dc.date.issued 2008-10-17
dc.identifier.uri http://dyuthi.cusat.ac.in/purl/4009
dc.description Spectrochimica Acta Part A 72 (2009) 474–483 en_US
dc.description.abstract Ten new copper(II) complexes of five potential bisthiocarbohydrazone and biscarbohydrazone ligands were synthesized and physico-chemically characterized. The spectral and magnetic studies of compounds are consistent with the formation of asymmetric di-, tri- or tetranuclear copper(II) complexes of deprotonated forms of respective ligands. The variable temperature magnetic susceptibility measurements of all complexes showantiferromagnetic interactions between the Cu(II) centers, in agreement with very broad powder EPR spectra. However, frozen solution EPR spectral studies are found in contradiction with the solid-state magnetic studies and indicate that the complexes are not very stable in solutions; the possible fragmentations of complexes are found in agreement with MALDI MS results. The EPR spectral simulation of most of the compounds is in agreement with the presence of two uncoupled Cu(II) species in solution. en_US
dc.description.sponsorship Cochin University of Science and Technology en_US
dc.language.iso en en_US
dc.publisher Elsevier en_US
dc.subject Thiocarbohydrazone en_US
dc.subject Carbohydrazone en_US
dc.subject Cu(II) complex en_US
dc.subject Dipyridyl ketone en_US
dc.subject Benzoylpyridine en_US
dc.subject Quinoline-2-carbaldehyde en_US
dc.subject Antiferromagnetism en_US
dc.subject EPR spectra en_US
dc.title Preparation, magnetic and EPR spectral studies of copper(II) complexes of an anticancer drug analogue en_US
dc.type Article en_US


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