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1.
Inorg Chem ; 45(3): 1277-88, 2006 Feb 06.
Artigo em Inglês | MEDLINE | ID: mdl-16441140

RESUMO

Four highly soluble square-planar Cu(II) and Ni(II) complexes of siloxy-salens (2SiCu, 2SiNi) and hydroxy-salens (2Cu, 2Ni) have been synthesized. An X-ray crystal structure analysis was performed on 2SiCu, 2SiNi, and 2Ni. The compounds have been investigated by cyclic voltammetry, UV-vis-NIR spectroelectrochemistry, and EPR spectroscopy. According to these results, the monooxidized species [2SiCu]+ and [2SiNi]+ are to be classified as Robin-Day class II and III systems, respectively. Magnetic measurements on the dinuclear (PMDTA)Cu(II) complex 1Cu2 x (PF6)2 with deprotonated 1,4-dihydroxy-2,5-bis(pyrazol-1-yl)-benzene (1) linker revealed antiferromagnetic coupling between the two Cu(II) ions thereby resulting in an isolated dimer compound. Coordination polymers [1Cu]n(H2O)(2n) of Cu(II) ions and bridging p-hydroquinone linkers were obtained from CuSO4 x 5 H2O and 1,4-dihydroxy-2,5-bis(pyrazol-1-yl)benzene. X-ray crystallography revealed linear chains running along the crystallographic a-direction and stacked along the b-axis. Within these chains, the Cu(II) ions are coordinated by two pyrazolyl nitrogen atoms and two p-hydroquinone oxygen atoms in a square-planar fashion.


Assuntos
Cobre/química , Hidroquinonas/química , Compostos Organometálicos , Cristalografia por Raios X , Eletroquímica , Ligantes , Magnetismo , Modelos Moleculares , Conformação Molecular , Níquel/química , Compostos Organometálicos/síntese química , Compostos Organometálicos/química , Sensibilidade e Especificidade , Espectrofotometria Infravermelho , Espectrofotometria Ultravioleta , Estereoisomerismo
2.
Acta Crystallogr C ; 58(Pt 1): i9-13, 2002 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-11781448

RESUMO

The crystal structure of the ambient-pressure phase of vanadyl pyrophosphate, (VO)2P2O7, has been precisely determined at 120 K from synchrotron X-ray diffraction data measured on a high-quality single crystal. The structure refinement unambiguously establishes the orthorhombic space group Pca2(1) as the true crystallographic symmetry. Moreover, it improves the accuracy of previously published atomic coordinates by one order of magnitude, and provides reliable anisotropic displacement parameters for all atoms. Along the a axis, the structure consists of infinite two-leg ladders of vanadyl cations, (VO)2+, which are separated by pyrophosphate anions, (P2O7)4-. Parallel to the c axis, the unit cell comprises two alternating crystallographically inequivalent chains of edge-sharing VO5 square pyramids bridged by PO4 double tetrahedra. No structural phase transition has been observed in the temperature range between 300 and 120 K.

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