2009
DOI: 10.1016/j.molcata.2008.12.021
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Synthesis, spectral, electrochemical and catalytic properties of Cu(II), Ni(II) and Co(II) complexes containing N, O donors

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Cited by 25 publications
(4 citation statements)
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“…This and further oxidation to a quinine-type oxidation product has been supported by EPR spectroscopy upon chemical oxidation with cerium sulfate for methoxy-substituted imino phenoxide Cu(II) complexes [ 52 ]. Complexes 1 , 2 , and 4 show similar electrochemical behaviors as described before with different degrees of reversibility of the oxidation reaction [ 52 , 55 ]. The oxidation potential of complex 3 is much higher than for the other complexes (Fig.…”
Section: Resultsmentioning
confidence: 80%
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“…This and further oxidation to a quinine-type oxidation product has been supported by EPR spectroscopy upon chemical oxidation with cerium sulfate for methoxy-substituted imino phenoxide Cu(II) complexes [ 52 ]. Complexes 1 , 2 , and 4 show similar electrochemical behaviors as described before with different degrees of reversibility of the oxidation reaction [ 52 , 55 ]. The oxidation potential of complex 3 is much higher than for the other complexes (Fig.…”
Section: Resultsmentioning
confidence: 80%
“…In continuation of our previous work on metal complexes containing imino phenoxide ligands, we describe herein the use of these ligands for the synthesis of four novel Cu(II) complexes. In principle, this class of complexes is well studied for different applications [ 38 55 ]. These complexes are easy to prepare and stable towards air and moisture and, therefore, they are much easier to handle compared to the sensitive polymerization catalysts based on 1st, 4th, 5th, and 13th group metals [ 3 7 ].…”
Section: Introductionmentioning
confidence: 99%
“…The IR spectrum of the free Schiff base ligand exhibits broad bands at 3050 and 3250 cm −1 , which are attributed to the stretching frequencies of aromatic hydroxyl substituent and allylic hydroxyl substituent. The disappearance of aromatic hydroxyl group band after complexation indicates the coordination through phenolic –OH with the central metal ion . The characteristic band around 3239 cm −1 remains in the spectra of the complexes and shows the non‐coordination of allylic –OH to the central metal ion.…”
Section: Resultsmentioning
confidence: 74%
“…[ 66 ] Similarly, the μ eff of the binuclear Cu (II) complex is 2.13 B. M, indicative of tetrahedrally distorted square planar geometry around the central metal ions, corresponding to one unpaired electron [ 67,68 ] such in the case of previously reported series of Cu (X‐DPMP) 2 complexes where [DPMP = 2‐[(2,6‐diisopropylphenylimino)methyl]phenol, X = Br, Cl, I]. [ 69 ] The stability of the H 2 L free ligand and the newly synthesized complexes were monitored over 24 h and there was slight or no change in their absorption spectra.…”
Section: Resultsmentioning
confidence: 98%