Acta Crystallographica Section E (Oct 2009)

{6,6′-Dimethoxy-2,2′-[ethane-1,2-diylbis(nitrilomethylidyne)]diphenolato-1κ4O1,O1′,O6,O6′:2κ4O1,N,N′,O1′}(ethanol-1κO)-μ-nitrato-1:2κ2O:O′-dinitrato-1κ4O,O′-samarium(III)zinc(II)

  • Qiang Huang,
  • Yu-Hua Sui,
  • Guo-Xiang Zhang

DOI
https://doi.org/10.1107/S1600536809033558
Journal volume & issue
Vol. 65, no. 10
pp. m1161 – m1162

Abstract

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In the title heteronuclear ZnII–SmIII complex, [SmZn(C18H18N2O4)(NO3)3(CH3CH2OH)], with the hexadentate Schiff base compartmental ligand N,N′-bis(3-methoxysalicylidene)ethylenediamine (H2L), the SmIII and ZnII ions are triply bridged by two phenolate O atoms from the Schiff base ligand and one nitrate anion. The five-coordinate ZnII ion is in a square-pyramidal geometry formed by the donor centers of two imine N atoms, two phenolate O atoms and one of the bridging nitrate O atoms. The SmIII center is in a ten-fold coordination of O atoms, involving the phenolate O atoms, two methoxy O atoms, one ethanol O atom, and two O atoms from two nitrate anions and one from the bridging nitrate anion. In the crystal, intermolecular O—H...O and C—H...O interactions generate a layer structure extending parallel to (101).