Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/40280
Title: Spectral and electrochemical behaviour of some copper(II) complexes with CuO4 chromophore
Authors: Palaniandavar, M
Anitha, N
Balasubramanian, S
Issue Date: Oct-1995
Publisher: NISCAIR-CSIR, India
Abstract: A few mixed ligand complexes of the type Cu(TCA)(L) [where TCA = trichloroacetic acid; L=2, 2, 6, 6-tetramethyl-3, 5-heptanedione (DPM), 2, 6-dimethyl-3, 5-heptanedione (DMHD) and o- hydroxybenzophenone (OHBP)] have been prepared and characterised by IR, electronic and EPR spectral data and compared with those of the corresponding CuL2 and other Cu(TCA)(L) chelates [where L=acetylacetone (ACAC), ethylacetoacetate (EAA), salicylaldehyde (SAL) and o-hydroxyacetophenone (OHAP)] to illustrate the nature of bonding of TCA with Cu(II). The Cull/CuI redox potentials of the bis-chelates vary in the order, DPM < DMHD < ACAC < EAA; SAL OHAP < OHBP; they shift towards more negative values as the number of electron repelling methyl groups increases. For mixed ligand complexes, the potentials are more positive than those of their respective bis-complexes and vary in the order, DPM > DMHD > ACAC > EAA: SAL < OHAP < OHBP. All the above results suggest that the replacement of L in CuL2 by TCA leads to a decrease in the delocalisation of electron density, more in o-hydroxyarylcarbonyl rather than in β-diketonate complexes.
Page(s): 803-808
URI: http://nopr.niscair.res.in/handle/123456789/40280
ISSN: 0975-0975(Online); 0376-4710(Print)
Appears in Collections:IJC-A Vol.34A(10) [October 1995]

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