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  • 1
    ISSN: 0009-2940
    Keywords: Tripod ligands ; Dinuclear cobalt complexes ; Dihydroxynaphthoquinones ; Dihydroxyanthraquinones ; Magnetism ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dinuclear Tripod Cobalt Complexes with Bridging 1,4,5,8-Tetraoxonaphthalene and 1,4,9,10-Tetraoxoanthracene Ligands: Structures, Spectroscopic, Magnetic, and Electrochemical PropertiesThe syntheses, structures, optical, magnetic, and redox properties of dinuclear tripodcobalt(II) complexes [tripod = CH3C(CH2PPh2)3] with briding 1,4,5,8-tetraoxonaphthalene 12- and 1,4,9,10-tetraoxoanthracene 22- are described. UV/Vis/NIR spectroscopy indicates interaction between the ligand and the metal orbitals. The magnetic interactions involving the two cobalt(II) centers and the bridging ligand are characterized by EPR spectroscopy and magnetic measurements and are analyzed in terms of qualitative Molecular Orbital calculations. The redox chemistry of these complexes is investigated by cyclic voltammetry and interpreted as metal-based oxidations and ligand-based reductions.
    Additional Material: 5 Tab.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 547-549 
    ISSN: 1434-1948
    Keywords: Copper ; Trinuclear ; Formamidines ; Magnetism ; Crystal structure ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In situ reaction of CuII triflate with aminopyridine or aminopyrimidine and triethylorthoformate in ethanol results in unique linear trinuclear CuII complexes with the general formula [Cu3(L-)4](CF3SO3)2(EtOH)x (L = dehydronated ligand N,N′-bis(pyridine-2-yl)formamidine or the new ligand N,N′-bis(pyrimidine-2-yl)formamidine). The structure [Cu-Cu-Cu angle 175.19(2)°] consists of four nearly flat molecules of the ligand which contribute to the propeller-type structure around the Cu-Cu-Cu axis. A strong antiferromagnetic interaction between the CuII ions is observed, resulting in an S = 1/2 ground state below 100 K.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2201-2207 
    ISSN: 1434-1948
    Keywords: Carboxylate syn-anti ; N-centered tripodal ligand ; Manganese ; Imidazole ; Helicoïdal inorganic chiral chain ; Magnetism ; π-π interaction ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The crystal structure of an infinite inorganic chain consisting of MnII and an N-centered tripodal ligand N,N-(2-pyridylmethyl)[(1-methylimidazol-2-yl)-methyl]glycinate is presented. It exhibits a chiral helical structure with a pitch of two monomeric units (each monomeric unit containing one Mn atom). Each manganese is connected to its neighbor through a carboxylate bridge in a syn-anti geometry. Around each manganese center, two carboxylates bind in a cis geometry. This peculiar bridging geometry (syn-anticis) provides a broken-line chain, running in a zig-zag manner along the b axis of the P21 space group. The magnetic properties have been investigated. They show a pseudo-2D magnetic structure, with one major pathway along the chain and an inter-chain minor one. The intrachain coupling is a weak antiferromagnetic interaction (J/k = -0.25). This low value is entirely consistent with the geometry of the bridge. The interchain coupling is a weaker antiferromagnetic coupling (J′/k = -0.11) and could be mediated through π-π interactions between pyridine and imidazole from two adjacent helixes.
    Additional Material: 4 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 1369-1375 
    ISSN: 1434-1948
    Keywords: Cluster ; Metal-rich antimonides ; Magnetism ; Sb-Sb bonds ; Structure and bonding ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The metal-rich antimonide Zr2V6Sb9 has been prepared by arc-melting of stoichiometric mixtures of Zr, V, and VSb2. Zr2V6Sb9 is the first example of a ternary ordered (filled) variant of the unusual V15Sb18 structure type. In addition to strong metal-antimony bonding, the crystal structure is significantly stabilized by bonding V-V and Sb-Sb interactions, whereas the Zr atoms do not form short metal-metal bonds. Band structure calculations using the Extended Hückel approximation reveal Zr2V6Sb9 being metallic, in agreement with the Pauli paramagnetism experimentally observed.
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  • 5
    ISSN: 1434-1948
    Keywords: Metal-rich antimonides ; Magnetism ; Structure and bonding ; Conductivity ; LMTO ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The title compounds can be synthesized in quantitative yields by arc-melting of stoichiometric amounts of HfSb2, Hf and one of the 3d metals V, Cr, Mn, Fe, Co, Ni, and Cu. These antimonides crystallize in a substitution variant of the W5Si3 type, in which one position is statistically mixed, occupied by the 3d metal atom M or the Sb2 atom in different ratios. Within the linear (M,Sb) chain, the M:Sb ratio may vary between 3:1 and 2:3. According to calculations of the electronic structures of Hf10MδSb6-δ with δ = 1, these phases are metallic compounds stabilized by strong Hf-Hf, Hf-M, and Hf-Sb bonds, and to a smaller extent by bonding interactions within the linear (M,Sb) chain. The metallic character was confirmed by measurements of the electrical resistivity and the magnetism of selected samples. Whereas Pauli paramagnetism was observed experimentally for M = V, Co, and Ni, Hf10FeSb5 is apparently the only phase with localized magnetic moments and magnetic coupling. This is in agreement with the magnetic ground state obtained solely for the ordered structure model of Hf10FeSb5 with spin-polarized calculation within the local spin density approximation.
    Additional Material: 9 Ill.
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  • 6
    ISSN: 1434-1948
    Keywords: Copper ; Trinuclear complexes ; Formamidines ; Magnetism ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Three new copper(II) linear trinuclear compounds are reported, all of which were synthesized in-situ, with the general formula [Cu3(L)4](CF3SO3)2(Y)x, where L is the dehydronated ligand: N,N′-bis(pyridine-2-yl)formamidine (abbreviated as Hpdf), N,N′-bis(pyrimidine-2-yl)formamidine (abbreviated as Hpmf) and N,N′-bis(5-methylpyridine-2-yl)formamidine (abbreviated as Hmpdf), Y = EtOH or H2O and x = 0.5-1.5. The compounds were characterized by X-ray diffraction, IR, LF, and EPR spectroscopy and by magnetic susceptibility down to 4 K. The structure of the compound [Cu3(pmf)4](CF3SO3)2(H2O)1/2 was determined by X-ray crystallography; it was found to crystallise in the triclinic space group P-1 with a = 8.529(5), b = 15.760(5), c = 19.639(5) Å, α = 101.793(5), β = 101.263(5), γ = 102.389(5)°, Z = 2. The structure [Cu-Cu-Cu angle 174.96(11)°] consists of four nearly flat molecules of the ligand, which contribute to the propeller-type structure around the Cu-Cu-Cu axis. A strong antiferromagnetic interaction between the CuII ions is observed with calculated J values, based on the Hamiltonian H = -2J(S1·S2 + S2·S3) - 2J′·S1·S3, of -174(1) cm-1, -120(1) cm-1, and -167(1) cm-1 for the compounds studied with L = pdf, pmf, and mpdf, respectively. These values are in agreement with an S = 1/2 ground state below temperatures of 120-160 K.
    Additional Material: 5 Ill.
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  • 7
    ISSN: 1434-1948
    Keywords: Crystal structures ; Nickel complexes ; Dinuclear complexes ; Magnetism ; Far-infrared ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The ligand bis(2-benzimidazolyl)propane coordinates to NiII with chloride as an anion, thereby forming a dinuclear compound with the formula: [NiCl2(tbz)2]2(C2H6O)2. This compound crystallizes in the space group P21/c. Each five-coordinated NiII ion has a distorted trigonal bipyramidal environment which consist of two asymmetrically bridging Cl anions with distances of 2.3556(17) and 2.4275(16) Å, a terminal Cl anion with a distance of 2.3496(17) Å and two nitrogen atoms of the ligand with distances of 2.022(4) and 2.000(4) Å. The Ni-Ni distance is 3.5891(12) Å, while the Ni-Cl-Ni angle is 97.23(6)°. The magnetic properties of the compound, as studied in the range 5-280 K, have been fitted with a zero-field splitting parameter D (-14.3 cm-1) and a ferromagnetic exchange between the Ni ions in the dinuclear unit (J = +2.5 cm-1). The title compound appears to be the second example for a five-coordinated ferromagnetic dinuclear NiII compound of this type, and its magnetic properties appear to correlate with the ligand structure. With the availability of an increasing number of examples of such species it appears that antiferromagnetic exchange is found for all cases with the chromophore N2ClNiCl2NiClN2 where the MN2 ring is 5-membered. In the case, where this ring is six-membered, the exchange is ferromagnetic.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, N.Y. : Wiley-Blackwell
    Journal of Cellular Biochemistry 19 (1982), S. 187-258 
    ISSN: 0730-2312
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
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  • 9
    ISSN: 0730-2312
    Keywords: fibronectin ; sponges ; Geodia cydonium ; aggregation ; cell recognition ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Experiments were carried out to test the hypothesis that fibronectin is involved in reaggregation of dissociated sponge cells. Cells from the siliceous sponge Geodia cydonium were extracted with urea to solubilize fibronectin from cells of higher multicellular organisms. The crude extract was further fractionated by DNA, heparin, and collagen affinity chromatography; they were termed Geodia fibronectinlike fractions. The fibronectinlike fractions contained a series of proteins with molecular weights different from that of the genuine fibronectin. The Geodia fibronectinlike fractions did not react with antiserum, produced against human fibronectin, under formation of a precipitin line. Using this antiserum the sponge cells could not be specifically labeled with FITC-anti-IgG antiserum. Radioimmunoprecipitation experiments revealed that the Geodia fractions contain - if at all - 0.1% fibronectin or fibronectinlike protein at the most. In the crucial experiments it was shown that the Geodia fibronectinlike fractions, human fibronectin, and antifibronectin antiserum exerted no influence on adhesion of Geodia cells either in the absence or in the presence of the soluble aggregation factor. Based on these findings, we conclude that fibronectin is apparently not present on Geodia cells and does not play a role in aggregation of this biological system.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, N.Y. : Wiley-Blackwell
    Journal of Cellular Biochemistry 19 (1982), S. 259-356 
    ISSN: 0730-2312
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
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