Single crystal X-ray crystal diffraction, IR and TGA-DTA data and searches
in the Cambridge Structural Database (CSD) have been used to analyze coordi
nation binding modes of Cd(II) in dicarboxylate complexes with anions of di
fferent length. The results, discussed in this paper, show that Cd(II) pres
ents a range of coordination geometries. Six, seven and eight coordination
with different degrees of departure from regular polyhedra are observed. Th
e length of the ions influences the availability of donor oxygens and induc
es bidentate, six or four member chelating rings, and monodentate binding,
which produces polymerization of different dimensionality.