2008
DOI: 10.1016/j.ica.2007.10.002
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Crystal structure and catalytic activity of a copper(II) complex based on a tetradentate bis-benzimidazole diamide ligand

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Cited by 23 publications
(11 citation statements)
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“…In addition, the bands are slightly blue shift and the energy enhanced with the ligand and ligand to metal charge transfer band (LMCT). A board much less intense d-d band in d 9 electron configuration is observed in the range of 600-800 nm, also indicating copper complexes exist in the solution (Mohapatra et al 2008;Bharti et al 2002).…”
Section: Synthesis and Characterization Of Complexesmentioning
confidence: 94%
“…In addition, the bands are slightly blue shift and the energy enhanced with the ligand and ligand to metal charge transfer band (LMCT). A board much less intense d-d band in d 9 electron configuration is observed in the range of 600-800 nm, also indicating copper complexes exist in the solution (Mohapatra et al 2008;Bharti et al 2002).…”
Section: Synthesis and Characterization Of Complexesmentioning
confidence: 94%
“…Recently, many synthetic mononuclear and dinuclear zinc(II) complexes [28][29][30][31][32] of ligands incorporating benzimidazoles have drawn much attention, because they are useful to elucidate the nature of the active site of the hydrolytic enzyme [28][29][30][31][32][33][34][35] and the catalytic mechanism.…”
Section: Introductionmentioning
confidence: 99%
“…N,N -bis(benzimidazolyl-2yl)(methyl)pentane diamide (GBGA). This ligand was synthesized using a procedure reported earlier [13]. The product was characterized by 1 H NMR spectra.…”
Section: Synthesis Of Ligand and Complexesmentioning
confidence: 99%
“…1 . N-octylation of GBGA to prepare O-GBGA was carried out as earlier [13]. GBGA (500 mg) was suspended in 20 ml of dry DMF and was stirred with dry K 2 CO 3 (350 mg) for 4-5 h on a water bath at a temperature of 70-75 • C. Octyl bromide (0.44 ml) was added to the turbid solution and was allowed to stir for next 72 h on a water bath at a temperature of 70-75 • C. Subsequently the solvent was stripped off on a rotary evaporator and the residue was extracted with chloroform.…”
Section: Synthesis Of Ligand and Complexesmentioning
confidence: 99%
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