







J. Appl. Cryst. (2001). 34, 710-714 [doi:10.1107/S0021889801012857]
Abstract: The crystal structures of isostructural 2,6-naphthalenedicarboxylate tetrahydrate salts of nickel(II) and cobalt(II) have been determined using Monte Carlo simulated annealing techniques and laboratory X-ray powder diffraction data. These compounds crystallize in the triclinic space group P
, with Z = 2; a = 10.0851 (4), b = 10.9429 (5), c = 6.2639 (3) Å,
= 98.989 (2),
= 87.428 (3),
= 108.015 (2)°, V = 649.32 (5) Å3 for [Ni(C12H6O4)(H2O)4], and a = 10.1855 (6), b = 10.8921 (6), c = 6.2908 (5) Å,
= 98.519 (4),
= 87.563 (4),
= 108.304 (3)°, V = 655.28 (8) Å3 for [Co(C12H6O4)(H2O)4]. The water-molecule H atoms were located by quantum chemical geometry optimization using CASTEP. The structure consists of alternating hydrocarbon and metal/oxygen layers parallel to the ac plane. Each naphthalenedicarboxylate anion bridges two metal cations; each carboxyl group is monodentate. The resulting structure contains infinite chains parallel to [111]. The octahedral coordination sphere of the metal cations contains trans carboxylates and four equatorial water molecules. The carboxyl groups are rotated by 15-20° out of the naphthalene plane. The metal/oxygen layers are characterized by an extensive hydrogen-bonding network. The orientations of the carboxyl groups are determined by the formation of short (O
O = 2.53 Å) hydrogen bonds between the carbonyl O atoms and the cis water molecules. Molecular mechanics energy minimizations suggest that coordination and hydrogen-bonding interactions are most important in determining the crystal packing.
Online 17 November 2001
![]() ![]() Structure factor file (CIF format) (136.8 kbytes) | |
![]() ![]() Structure factor file (CIF format) (137.7 kbytes) | |
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