Double salts are ionic compounds formed by the combination of two simple salts, but they retain their individual identities in solution. These compounds do not involve coordinate bonds.
For example: \[ \mathrm{K_2SO_4 \cdot Al_2(SO_4)_3} \] is a double salt.
In contrast, complex compounds consist of a central metal ion bonded to ligands through coordinate covalent bonds. These ligands donate electron pairs to the metal.
Example of a complex compound: \[ [\mathrm{CoCl_2(en)_2}]SO_4 \] where "en" stands for ethylenediamine, a ligand.
- Didentate ligands are ligands that can bind to a metal atom or ion through two donor atoms simultaneously. An example is ethylenediamine (en), which uses both nitrogen atoms to bind to the metal.
- Ambidentate ligands have two potential donor atoms, but can coordinate through only one atom at a time. A classic example is the thiocyanate ion: \[ \mathrm{SCN^-} \] It can bind to the metal via the sulfur atom (S-bound) or the nitrogen atom (N-bound), but not both at once.
Werner’s coordination theory in 1893 was the first attempt to explain the bonding in coordination complexes. It must be remembered that this theory was put forward before the electron had been discovered by J.J. Thomson in 1897, and before the electronic theory of valency. Werner did not have any of the modern instrumental techniques and all his studies were made using simple experimental techniques. Werner was able to explain the nature of bonding in complexes and he concluded that in complexes, the metal shows two different sorts of valency: primary and secondary. Primary valences are normally ionisable whereas secondary valences are non-ionisable.
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