“…Thus rigid carboxylate ligands have been widely used for the design and synthesis of avariety of structures [4]. Among these carboxylatebase complexes, nickel(II) representatives have attracted great attention since nickel has been recognized as aconsiderably important biological agent forming the active site of av ariety of metalloproteins, such as hygrogenase (H 2-ase), carbon monoxide dehydrogenase (CODH), S-methyl-coenzyme Mm ethylreductase (MCR) and urease [5,6]. In addition, their adducts with nitrogen have potential applications in area of organic conductors and magnetic materials [7].…”
Source of materialAm ixed solution of 6-hydroxy-3-pyridazinecarboxylic acid (0.05 mmol) and NiCl 2 · 6H 2 O(5mmol) in distilled water (10 ml) in the presence of excess 2,6-dimethylpyridine (ca. 0.05 ml for adjusting the pH value to the basic condition) was stirred for 5min.
Experimental detailsAll the hydrogen atoms were included in calculated positions and treated as riding with
DiscussionThe rational design and construction of coordination complexes based upon assembly of metal ions and multifunctional organic ligands is an interesting research field. This not only stems from their potential application as functional materials but also from their intriguing structural features [1][2][3]. In principle, the structural motifs of these molecular assemblies are defined by the
“…Thus rigid carboxylate ligands have been widely used for the design and synthesis of avariety of structures [4]. Among these carboxylatebase complexes, nickel(II) representatives have attracted great attention since nickel has been recognized as aconsiderably important biological agent forming the active site of av ariety of metalloproteins, such as hygrogenase (H 2-ase), carbon monoxide dehydrogenase (CODH), S-methyl-coenzyme Mm ethylreductase (MCR) and urease [5,6]. In addition, their adducts with nitrogen have potential applications in area of organic conductors and magnetic materials [7].…”
Source of materialAm ixed solution of 6-hydroxy-3-pyridazinecarboxylic acid (0.05 mmol) and NiCl 2 · 6H 2 O(5mmol) in distilled water (10 ml) in the presence of excess 2,6-dimethylpyridine (ca. 0.05 ml for adjusting the pH value to the basic condition) was stirred for 5min.
Experimental detailsAll the hydrogen atoms were included in calculated positions and treated as riding with
DiscussionThe rational design and construction of coordination complexes based upon assembly of metal ions and multifunctional organic ligands is an interesting research field. This not only stems from their potential application as functional materials but also from their intriguing structural features [1][2][3]. In principle, the structural motifs of these molecular assemblies are defined by the
“…These complexes can serve as potent antitumor, antiviral and antibacterial agents [5]. Among these Schiff-base complexes, nickel(II) representatives have attracted great attention since nickel has been recognized as aconsiderably important biological agent forming the active site of avariety of metalloproteins, such as hygrogenase(H 2 -ase), carbon monoxide dehydrogenase (CODH), S-methyl-coenzyme-M methylreductase (MCR) and urease [6][7][8]. In addition, their adducts with nitrogen have potential applications in area of organic conductors and magnetic materials [9].…”
“…Acetonitrile also acts as a strongly differentiating solvent with a modest solvating power for many polar ionic solutes (Aktas et al, 2006). Co(II), Ni(II) and Cu(II) are associated with several enzymes and any variation in their concentrations leads to metabolic disorders (Kolodziej, 1994). Hence, the speciation of Co(II), Ni(II) and Cu(II) complexes of L-valine in varying compositions of acetonitrile-water mixtures have been studied.…”
Chemical speciation of binary complexes of Co(II), Ni(II) and Cu(II) with L-valine in 0.0-60.0% v/v acetonitrile-water mixtures was studied pH-metrically at an ionic strength of 0.16 mol L -1 at 303.0 K. The existence of different binary complexes was established from the modelling studies, using the computer program MINIQUAD75. The appropriateness of the model was ascertained by studying the effect of errors in concentrations of the reagents. The trend in variation of stability constants with change in the permittivity of the medium is explained on the basis of electrostatic and non-electrostatic forces. The species distribution diagrams and the plausible equilibria for the formation of the species are also presented.
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