Abstract
Some physicochemical properties of 2-chloro-4-nitrobenzoates of Co(II), Ni(II), and Cu(II) were studied. The complexes were obtained as mono-and dihydrates with a metal ion—ligand mole ratio of 1: 2. All complexes are polycrystalline compounds. Their colours depend on the kind of central ion: pink for Co(II) complex, green for Ni(II), and blue for Cu(II) complexes. Their thermal decomposition was studied only in the range of 293 K–523 K because it was found that on heating in air above 523 K 2-chloro-4-nitrobenzoates decompose explosively. Hydrated complexes lose crystallization water molecules in one step. During dehydration process no transformation of the nitro group to nitrito one took place. Their solubilities in water at 293 K are of the orders of 10−3-10−2 mol dm−3. The magnetic moment values of 2-chloro-4-nitrobenzoates determined in the range of 76 K–303 K change from 3.48µB to 3.82µB for Co(II) complex, from 2.24µB to 2.83µB for Ni(II) 2-chloro-4-nitrobenzoate, and from 0.31µB to 1.41µB for Cu(II) complex. 2-Chloro-4-nitrobenzoates of Co(II) and Ni(II) follow the Curie—Weiss law, but the complex of Cu(II) forms dimer.
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© 2006 Institute of Chemistry, Slovak Academy of Sciences
Articles in the same Issue
- Calibrationless determination of electroactive species using chronoamperograms at collector segment of interdigitated microelectrode array
- The β-carotene dilemma: ESR study with coordinated peroxyl radicals
- Determination of 5-hydroxymethylfurfural after Winkler and by the HPLC method for authentication of honey
- A simple linear sweep voltammetric method for the determination of double-stranded DNA with malachite green
- Spectral and electrochemical study of coordination molecules Cu4OX6L4: 3-Pyridylmethanol and 4-pyridylmethanol Cu4OBrnCl(6−n)(pm)4 complexes
- Magnetic, spectral, and thermal behaviour of 2-chloro-4-nitrobenzoates of Co(II), Ni(II), and Cu(II)
- Synthesis, characterization, and biological activities of some transition metal(II) complexes with the thiosemicarbazone derived from 4-[1-(4-methylphenylsulfonyl)-1H-indol-3-yl]but-3-en-2-one
- Crystal structure and thermal chemical properties of 2-(2,4-dimethylanilino)-3-methyl-6-diethylaminofluorane
- Etherification of glycerol with tert-butyl alcohol catalysed by ion-exchange resins
- Synthesis and reactions of 2-and 4-substituted furo[3,2-c]pyridines
- Synthetic approaches towards bisspiro[naphthalene-2(1H),3′-(3H)pyrazol]-1-one-containing compounds
- Mild Pfitzner—Moffat oxidation of the (1→3)-β-D-glucan from Saccharomyces cerevisiae
- Limited sample recovery in coupled methods of high-performance liquid chromatography of synthetic polymers
Articles in the same Issue
- Calibrationless determination of electroactive species using chronoamperograms at collector segment of interdigitated microelectrode array
- The β-carotene dilemma: ESR study with coordinated peroxyl radicals
- Determination of 5-hydroxymethylfurfural after Winkler and by the HPLC method for authentication of honey
- A simple linear sweep voltammetric method for the determination of double-stranded DNA with malachite green
- Spectral and electrochemical study of coordination molecules Cu4OX6L4: 3-Pyridylmethanol and 4-pyridylmethanol Cu4OBrnCl(6−n)(pm)4 complexes
- Magnetic, spectral, and thermal behaviour of 2-chloro-4-nitrobenzoates of Co(II), Ni(II), and Cu(II)
- Synthesis, characterization, and biological activities of some transition metal(II) complexes with the thiosemicarbazone derived from 4-[1-(4-methylphenylsulfonyl)-1H-indol-3-yl]but-3-en-2-one
- Crystal structure and thermal chemical properties of 2-(2,4-dimethylanilino)-3-methyl-6-diethylaminofluorane
- Etherification of glycerol with tert-butyl alcohol catalysed by ion-exchange resins
- Synthesis and reactions of 2-and 4-substituted furo[3,2-c]pyridines
- Synthetic approaches towards bisspiro[naphthalene-2(1H),3′-(3H)pyrazol]-1-one-containing compounds
- Mild Pfitzner—Moffat oxidation of the (1→3)-β-D-glucan from Saccharomyces cerevisiae
- Limited sample recovery in coupled methods of high-performance liquid chromatography of synthetic polymers