(a) In both complexes, Ni is in +2 oxidation state with a valence shell electronic configuration of 3d8. In the presence of weak field water ligands, two unpaired electrons do not pair up. Hence, the complex [Ni(H2O)6]+2 has two unpaired electrons which result in green colour. Due to d-d transition, red light is absorbed and complimentary light emitted is green.
However, due to the presence of (en) which is a strong field ligand, the splitting is increased. Due to the change in
t2g - eg splitting the colouration of the compound changes from green to blue.
(b) The given complex, tris(ethane-1,2–diamine) cobalt(III) sulphate, contains cobalt (Co3+) as a central metal ion. There are three ethane-1, 2-diamine (en) ligand as the multiplicative prefix 'tris' is used. The complex ion has sulphate ion (SO42-) as a counter ion. Therefore, the formula of the compound becomes [Co(H2NCH2CH2NH2)3]2(SO4)3.
OR
(a) The electronic configuration of the central metal ion in a coordination entity t2g3 eg1 indicates that the fourth electron enters one of the eg orbitals, since, ∆o < P. As there are four unpaired electrons in the complex, it is a high spin complex molecule.
(b) The splitting of degenerate orbitals by the ligands into orbitals of different energy is called crystal field splitting. When the metal ion is surrounded by six ligands in octahedral directions, the d-orbitals will split into a set of two higher energy eg (dx2 - y2, dz2) orbitals and another set of three lower energy t2g (dxy, dyz, dzx) orbitals. The electronic configuration of the central metal ion in a coordination entity t2g3 eg1 indicates that the fourth electron enters one of the eg orbitals, since, ∆o < P. As there are four unpaired electrons in the complex, it is a high spin complex molecule. The crystal field splitting diagram is shown below:
