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  • 1995-1999  (2)
  • Chemistry  (2)
  • exchange coupling  (2)
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  • 1
    ISSN: 0947-6539
    Keywords: bridging ligands ; coordination ; copper compounds ; exchange coupling ; magnetic properties ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Magnetic long-range exchange coupling between two unpaired electrons of two copper(II) ions in a square-pyramidal ligand environment (dx2-y2)1, which are rigidly separated by 〉 10 Å by an organic spacer ligand (e.g., a μ-dicarboxylato ligand) has been systematically studied. The following complexes have been synthesized: [{LCu(OH2)}2(μ-terephthalato)](ClO4)2 (I), [LCuII(OH2)(benzoato)](CIO4) (2), [{LCuII(NCS)}2(μ-terephthalato)]-2 CH3OH (3), [{LCuII(NCS)}2 (μ-4,4′-oxybisbenzoato)] · 3 CH3OH (4), [{LCuII(OH2)}2 (μ-tetrafluoroterephthalato)](CIO4)2 (5), [{LCuII(OH2)}2{LCuII}2 (μ-tetrafluorobenzoato)3](CIO4)2 · 6 H2O (6), [{LCuII(OH2)}2 (μ-biphenyl-4,4′-dicarboxylato)](CIO4)2 (7), [LCuII(μ-biphenyl-4,4′-dicarboxylato)]n (HZO)2n (8), [{LCuII(NCS)}2 (μ-biphenyl-4.4′-dicarboxylato)] (9), [{LCu(OH2)}2, (μ-trans,trans-2,4-hexadien1,6-dicarboxylato)] (CIO4)2 (10) (L = 1,4,7-trimethyl-1,4,7-triazacyclononane). Complexes 1, 2, 3, 4, and 6 have been characterized by X-ray crystallography; the structure of 1 has been described previously.[15] Temperature-dependent magnetic susceptibility data for all complexes have been measured over the range 2.0-298 K. In complexes 2, 3, 4, 6, 8, and 9 only very weak, if any, intermolecular antiferromagnetic or, in the case of 6, ferromagnetic coupling has been observed (|J|≤2cm-1; H= -2JS1 S2 S1 = S2 = 1/2). In contrast, in complexes 5 (2J=-80cm-1), 7(2J=-62cm-1), and 10 (2J = -100 cm-1) relatively strong intramolecular antiferromagnetic exchange coupling has been detected. The intramolecular Cu…Cu separation is 11.3Å in 5, 15.6 Å in 7, and approximately 12.0Å in 10. These data demonstrate that intramolecular antiferromagnetic exchange coupling of considerable magnitude is possible over distances 〉 15 Å, provided that the effective magnetic orbitals are favorably aligned.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0947-6539
    Keywords: EPR spectroscopy ; exchange coupling ; iron ; Moessbauer spectroscopy ; O ligands ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An asymmetric triangular FeIII complex has been synthesized by an unusual FeII-promoted activation of salicylaldoxime. Formation of the ligand 2-(bis(salicylideneamino)methyl)phenol in situ is believed to occur through the reductive deoximation of salicylaldoxime by ferrous ions. The trinuclear ferric complex has been characterized on the basis of elemental analysis, IR, variable-temperature magnetic susceptibility, and EPR and Mössbauer spectroscopies. The molecular structure established by X-ray diffraction consists of a trinuclear structure with a [Fe3(μ3-O)(μ2-OPh)]6+ core. Two iron ions are in a distorted octahedral environment having FeN2O4 coordination spheres, and the five-coordinated third iron ion, with an FeNO4 coordination sphere, is in a trigonal bipyramidal environment. The magnetic susceptibility measurements revealed an St = 5/2 ground state with the antiparallel exchange interactions J = - 34.3 cm-1, J' = - 4.7 cm-1, and D = - 0.90 cm-1. The EPR results are consistent with a ground state of S = 5/2 together with a negative D5/2 value. The Mössbauer isomer shifts together with the quadrupole splitting also provide evidence for the high-spin state of the three ferric sites. Magnetic Mössbauer spectra lead to the conclusion that the internal magnetic fields possibly lie in the plane of the three ferric ions.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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