Give the oxidation state, d-orbital occupation and coordination number of the central metal ion in the following complexes:
K3[Co(C2O4)3]
(NH4)2[CoF4]
Cis−[Cr(en)2Cl2]Cl
[Mn(H2O)6]SO4
K3[Co(C2O4)3]
(+1)3+x+(−2)×3=0 +3+x−6=0 x=+3
Thus, Co is present as Co3+
Co27 = [Ar]3d74s2
Co3+ = [Ar]3d6 so d-orbital occupation is d6 or t62g e0g
(as C2O2−4 is strong field ligand)
Coordination Number of Co = 3×denticity of C2O4
=3×2 (as C2O2−4 is a bidentate ligand)= 6
(NH4)2[CoF4]
(+1)×2x+(−1)×4=0 2+x−4=0 x=+2
Thus, Co is present as Co2+
Co2+=[Ar]3d7 so, d-orbital occupation is d7 or t52g e2g
(as F− is a weak field ligand)
CN of Co = 4
Cis−[Cr(en)2Cl2]Cl
x=(0)2+(−1)×2+(−1)=0 x+0−2−1=0 x=+3
Thus, Cr is present as Cr3+.
Cr3+=[Ar]3d3 so, d-orbital occupation is d3 or t32g, eg0
CN of Cr =2×x denticity of en +2=2×2+2=6
[Mn(H2O)6]SO4
x+(0)6+(−2)=0 x=+2
Thus, Mn is present as Mn2+.
Mn2+=[Ar]3d5 So, d-orbital occupation is d5 or t32g e2g
CN of Mn = 6