Abstract
The compound Lco2Br3,2H2O (where L is a binucleating ligand derived from the macrocycle
LH2 formed by condensation of two molecules each of propane-1,3-diamine and 2-hydroxy-5-
methylisophthalaldehyde) was found to occur in two crystalline forms. The structures of both have
been determined by single-crystal X-ray diffraction techniques, revealing that each corresponds to a
different geometrical isomer of composition Lco2Br3,2H2O. Each structure was determined by the
conventional Patterson-Fourier method and refined by a least-squares procedure, with only the
Co, Br, N and O atoms being refined anisotropically. The first form, designated the A-isomer,
crystallizes in the orthorhombic space group Pn21a with four formula units in a cell of dimensions
a 15.173(1), b 17.370(2) and c 10.493(1) Ǻ. The structure refined to a conventional R-factor of
0.074 by means of 1883 unique reflections collected by counter methods. The second form, or
B-isomer, crystallizes in the monoclinic space group P21 with two formula units in a cell of dimen-
sions a 10.676(1), b 15.235(2), c 9.304(1) Ǻ and β 111.83(2)°. The structure refined to a conventional
R-factor of 0.101 by means of 2006 independent reflections collected by counter methods. Both
isomers are composed of discrete bromide anions together with discrete binuclear cations of com-
position [Lco2Br2,2H2O]+, each containing one cobalt(II) and one cobalt(III) atom with a Co...Co
distance of 3.13 Ǻ. In both isomers the cobalt atoms are in octahedral environments. In the
A-isomer two bromine atoms are bonded to the cobalt(III) atom in positions perpendicular to the
ligand N2O2 donor plane, with the two water molecules occupying similar positions about the
cobalt((II). But in the B-isomer, one water molecule and one bromine atom are bonded to each of
the cobalt(III) and the cobalt((II) atoms in the comparable positions. In both structures the ionic
bromide is involved in a hydrogen-bonding scheme with the coordinated water molecules.
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