Acta Crystallographica Section E (Nov 2009)

Poly[(6-carboxypicolinato-κ3O2,N,O6)(μ3-pyridine-2,6-dicarboxylato-κ5O2,N,O6:O2′:O6′)dysprosium(III)]

  • Xu Li,
  • Qing-Yang Lian,
  • Qiu-Hui Meng,
  • Yi-Fan Luo,
  • Rong-Hua Zeng

DOI
https://doi.org/10.1107/S1600536809039075
Journal volume & issue
Vol. 65, no. 11
pp. m1288 – m1289

Abstract

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In the title complex, [Dy(C7H3NO4)(C7H4NO4)]n, one of the ligands is fully deprotonated while the second has lost only one H atom. Each DyIII ion is coordinated by six O atoms and two N atoms from two pyridine-2,6-dicarboxylate and two 6-carboxypicolinate ligands, displaying a bicapped trigonal-prismatic geometry. The average Dy—O bond distance is 2.40 Å, some 0.1Å longer than the corresponding Ho—O distance in the isotypic holmium complex. Adjacent DyIII ions are linked by the pyridine-2,6-dicarboxylate ligands, forming a layer in (100). These layers are further connected by π–π stacking interactions between neighboring pyridyl rings [centroid–centroid distance = 3.827 (3) Å] and C—H...O hydrogen-bonding interactions, assembling a three-dimensional supramolecular network. Within each layer, there are other π–π stacking interactions between neighboring pyridyl rings [centroid–centroid distance = 3.501 (2) Å] and O—H...O and C—H...O hydrogen-bonding interactions, which further stabilize the structure.