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  • 1
    ISSN: 1434-4475
    Keywords: Aminopyridines ; Dicyanamide complexes ; ESR spectra ; Ligand field spectra ; Magnetic moments
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary New dicyanamide complexes of the typeM[N(CN)2]2 L 2 (M=Cu or Ni;L=2-, 3-, 4-aminopyridine, 2-amino-5-nitropyridine) and Co[N(CN)2]2 (2-amino-5-nitropyridine)2 were prepared and studied by spectroscopic methods as well as by room-temperature magnetic moments. The results show that the Cu(II) complexes have elongated pseudooctahedral structures while the Ni(II) and Co(II) complexes are octahedral. In most cases the N(CN)2 groups are in bridging function and through their cyanide nitrogens, or-more rarely-amide and cyanide nitrogens connect the basic structure units into polymeric conglomerates. In the Cu(II) systems exchange coupling is seen from the μeff value or ESR spectrum.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 112 (1981), S. 1143-1153 
    ISSN: 1434-4475
    Keywords: Alkylpyridines ; Cyanatocopper(II)complexes ; ESR spectra ; Solid state electronic spectra ; Torsional isomers
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract New cyanato-copper(II) complexes of the type Cu(NCO)2 L 2 (L=2,3-, 2,5-, 3,4- or 3,5-lutidine, 3- or 4-ethylpyridine) and Cu(NCO)2 L (L=2,3- or 2,5-lutidine, 2-ethylpyridine) were prepared. Solid state electronic, ESR and IR spectral results show, that Cu(NCO)2 L 2 complexes have tetragonal structures varying from pseudooctahedral to practically planar forms, also involving a square-pyramidal arrangement. The β-form of Cu(NCO)2(2-picoline)2 was isolated and found to be a distortion isomer of the known α-form. According to physical results, Cu(NCO)2 L complexes exhibit highly distorted five-coordinate structures. Further knowledge about the influence of type, number and position ofL ligand alkyl groups on the structure-bonding properties of cyanato-copper(II) complexes was obtained.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1572-901X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary New cyanato-copper(II) complexes with aminopyridines (ampy) were prepared and studied;viz. Cu(NCO)2(3-ampy)2 (α- and β-form), Cu(NCO)2(3-ampy)2(H2O), Cu(NCO)2(4ampy)2, and Cu(NCO)2(2-ampy). According to physical results, the Cu(NCO)2L2 complexes exhibitpseudo-octahedral structures with amine nitrogens or cyanate oxygens occupying axial sites. For α- and β-Cu(NCO)2(3-ampy)2 the crystal structure reorganization is connected with a change in axial distortion. The compound Cu(NCO)2(2-ampy) is square pyramidal or — more probably — rhombic octahedral and its strong antiferromagnetism reveals the N-bridging function of the NCO groups.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1572-901X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary New coligand isomers of composition Cu{N(CN)2}2(pz)2 and Cu{pz · N(CN)2}2 (pz = pyrazole) were prepared and studied by measuring their magnetic susceptibilities up to 4.2K and by aid of their e.s.r., ligand field and i.r. spectra. The susceptibility data have been analysed with various models for the exchange-coupled copper(II) polymers. It is shown that the resultant exchange coupling is ferromagnetic for Cu{N(CN)2}2(pz)2 (J ∼ 1.1 - 1.4 cm−1) but antiferromagnetic for Cu{pz · N(CN)2}2 (J ≈ −0.4 cm−1). A polymeric chain structure is proposed for Cu{N(CN)2}2(pz)2 havingpseudo-octahedrally coordinated copper(II) and CN-bridging dicyanamide ligands. Its coligand isomer contains anionic chelate ligands, formed by nucleophilic addition between N(CN)2 and pz in the copper(II) coordination sphere, and giving with this central atom a square-planar system. Definite, but slight axial interaction takes place between these structure units.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1572-901X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Dicyanamide complexes of CuII, NiII and CoII of the type M[N(CN)2]2L2, where L = benzimidazole, 2-methyl- or 2-ethylbenzimidazole, have been prepared and studied by spectroscopy and magnetochemistry. The complexes, except for Co[N(CN)2]2 (benzimidazole)2, are six-coordinate, involving bidentate bridging dicyanamide groups. While the NiII complexes have practically octahedral structures, the CuII complexes are pseudooctahedral with similar tetragonal distortion. The ligand field strength in these complexes depends mainly on the steric effect of the benzimidazole ligands. The CoII complex of benzimidazole is monomeric tetrahedral, but that of 2-ethylbenzimidazole is tetragonal octahedral. The oridging function of dicyanamide in the six-coordinate complexes is realized either through both cyanide or through amide and cyanide nitrogens. The complex Cu[N(CN)2]2 (2-methylbenzimidazole)2 is a weak antiferromagnet (J = -0.1 cm−1), exhibiting under ca. 15 K a long-range antiferromagnetic ordering.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1572-901X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Reaction of CoII with N(CN) inf2 sup− or C(CN) inf3 sup− in the presence of imidazole (iz) or its methyl derivatives (2-meiz and 4-meiz) gave eight compounds of CoII: ligand stoichiometry 1∶2, including two isomeric pairs (α and β) for the complexes [Co{C(CN)3}2(2-meiz)2] and [Co{C(CN)3}2-(4-meiz)2]. The complexes were studied by electronic and i.r. spectroscopies. For α-[Co{C(CN)3}2(2-meiz)2] singlecrystal X-ray analysis was performed; its crystal structure consists of one-dimensional chains, formed by C(CN) inf3 sup− anions bridging between the CoII atoms. The CoII atom is nearly octahedrally coordinated by two tertiary nitrogens of 2-meiz and four nitrogens of C(CN) inf3 sup− . The spectra of these compounds and of the complexes with iz, as well as that of α-[Co{C(CN)3}2(4-meiz)2], indicate all these compounds to have basically the same bridging polymeric octahedral structure. However, the spectra indicate distorted tetrahedral structures for the remaining compounds.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1572-901X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The systems MII-ONC(CN)2 −-L-MeOH-H2O [M = Ni, Cu, Co or Pd; L = pyrazole (pz)] were studied to determine conditions for the nucleophilic addition of MeOH to nitrosodicyanomethanide (ndcm)− in the metal coordination sphere. Compounds containing two or three bidentate anionic chelate ligands derived from methyl-2-cyano-2-(hydroxyimino)ethanimidic acid, H(mcoe), formed by nucleophilic addition of MeOH to ONC(CN)2 −, were isolated: [Cu(mcoe)2(H2O)2] (elongated pseudo-octahedron with two water molecules at long axial distances), [Co(mcoe)3] (approximate octahedron) and [Pd(mcoe)2] (square-planar). In the CoII system, oxidation to CoIII took place. In addition, simple nitrosodicyanomethanide compounds [Ni(ndcm)2(pz)4] (nearly octahedral) and [Pd(ndcm)2(pz)2] (square-planar) were obtained. The crystal structure of trans-[Ni(ndcm)2(pz)4] has been elucidated by X-ray crystallography. The NiII atom is nearly octahedrally coordinated by four nitrogens of pz and two oxygens of (ndcm)−. This compound is the first example of a transition metal oxygen-coordinated nitrosodicyanomethanide complex with a short metal-oxygen bond. The remaining compounds were characterized by i.r. and electronic spectra.
    Type of Medium: Electronic Resource
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