Ni +2 + 2Dmg– → [Ni(Dmg) 2 ] Dimethyl glyoxime act as bidentate ligand.
Coordination Compounds
For low spin d 6 complex electronic configuration =
x = 6, y = 0, z = 3 C.F.S.E. = (– 0.4 × 6 + 0 × 0.6)
0 + 3P =
Those orbitals which utilizes 3d-orbitals for bonding and exhibit paramagnetic behaviour forms outer orbital complex.
Ni +2 = [Ar] 3d 8 4s 0 It forms outer orbital complex. (b) [Zn(NH 3 ) 6 ] 2+ outer orbital complex but diamagnetic (c) [Cr(NH 3 ) 6 ] 3+ inner orbital complex but paramagnetic (d) [Co(NH 3 ) 6 ] 3+ inner orbital complex but diamagnetic
Due to positive oxidation state of Mn back donation in π* ABMO of CO is minimum therefore C–O bond is strongest.
[Cr(NH 3 ) 6 ] +3 [Ar] 3d 3 4s 0 three unpaired electron are present in t 2g orbited
[Mn(H 2 O) 6 ] 2+ : Mn 2+ = 3d 5 Number of unpaired electron = 5 [Fe(H 2 O) 6 ] 2+ : Fe 2+ = 3d 6 Number of unpaired electrons = 4 [Co(H 2 O) 6 ] 2+ : Co 2+ = 3d 7 Number of unpaired electrons = 3 [Cr(H 2 O) 6 ] 2+ : Cr 2+ = 3d 4 Number of unpaired electrons = 4 Minimum paramagnetic behaviour is shown by [Co(H 2 O) 6 ] 2+ .
Coordination isomerism arises from the interchange of ligands between cationic and anionic entities of different metal ions present in the complex.
[Co (NH 3 ) 6 ] [Cr(CN) 6 ] is an isomer of [Co(CN) 6 ] [Cr(NH 3 ) 6 ]
Complexes of the type M ABCD may exist in three isomeric forms.
Similarly, [Pt(Py)(NH 3 )BrCl] may exist in three isomeric form in which M = Pt, A = Py, B = NH 3 , C = Br, D = Cl.
Ti 3+ [Ar] 3d 1 4s 0 (1 unpaired electron) Cr 3+ [Ar] 3d 3 4s 0 (3 unpaired electrons) Co 3+ [Ar] 3d 6 4s 0 (0 unpaired electrons because of pairing) Zn 2+ [Ar] 3d 10 (no unpaired electrons) [Cr(NH 3 ) 6 ] 3+ exhibits highest paramagnetic behaviour as it contains 3 unpaired electrons.
As + ve charge on the central metal atom increases, the less readily the metal can donate electron density into the * orbitals of CO ligand to weaken the C – O bond.
Hence, the C – O bond would be strongest in Mn(CO) 6 + .