Literature DB >> 2354044

The structure of hexaaquanickel(II) chlorate.

J C Gallucci1, R E Gerkin.   

Abstract

Hexaaquanickel(II) chlorate, [Ni(H2O)6]-(ClO3)2, Mr = 333.69, cubic, Pa3-, a = 10.3159 (5) A, V = 1097.80 (5) A3, Z = 4, F(000) = 680, Dx = 2.02 g cm-3, lambda(Mo K alpha-) = 0.71069 A, T = 296 K, mu = 23.13 cm-1, R = 0.026 for 388 unique reflections having I greater than sigma I. The single type of Ni ion is coordinated by six water-molecule O atoms, each at an observed distance 2.054 (1) A, in an almost regular octahedral array. The single type of chlorate ion has a Cl--O bond length 1.487 (1) A and O--Cl--O bond angle 106.45 (6) degrees. The Ni--O complex, but not the chlorate ion, manifested rigid-body behavior. The Ni--O distance corrected for rigid-body motion is 2.060 A. Location and refinement of the two inequivalent H atoms permitted a detailed analysis of hydrogen bonding, which occurs principally between the oxygen octahedra and the chlorate groups.

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Year:  1990        PMID: 2354044     DOI: 10.1107/s0108270189006943

Source DB:  PubMed          Journal:  Acta Crystallogr C        ISSN: 0108-2701            Impact factor:   1.172


  1 in total

1.  Hydration energies of divalent metal ions, Ca2+ (H2O)n (N = 5-7) and Ni2+ (H2O)m (N = 6-8), obtained by blackbody infrared radiative dissociation.

Authors:  S E Rodriguez-Cruz; R A Jockusch; E R Williams
Journal:  J Am Chem Soc       Date:  1998-06-17       Impact factor: 15.419

  1 in total

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