Write down the IUPAC name for each of the following complexes and indicate the oxidation state, electronic configuration and coordination number. Also give stereochemistry and magnetic moment of the complex:
\((i) K[Cr(H_2O)_2(C_2O_4)_2].3H_2O\)
\((ii)[Co(NH_3)_5Cl]Cl_2\)
\((iii) CrCl_3(py)_3\)
\((iv) Cs[FeCl_4]\)
\((v)K_4[Mn(CN)_6]\)
(i) Potassium diaquadioxalatochromate (III) trihydrate.
Oxidation state of chromium=3
Electronic configuration: \(3d ^{3} : t_{2g}^ 3 \)
Coordination number = 6 Shape: octahedral
Stereochemistry:
Magnetic moment, \(ÃŽÂ\frac{1}{4}=\sqrt{n(n+2)}\)
\(=\sqrt{3(3+2)}\)
\(=\sqrt{15}\)
\(∼ 4BM\)
\((ii) [Co(NH_3)_5Cl]Cl_2 \)
IUPAC name: Pentaamminechloridocobalt(III) chloride
Oxidation state of \( Co=+3 \)
Coordination number=6 Shape: octahedral.
Electronic configuration: \(d ^{6} : t_{2g}^ 6 .\)
Stereochemistry:
Magnetic Moment=0
\((iii) CrCl_3(py)_3 \)
IUPAC name: Trichloridotripyridinechromium (III)
Oxidation state of chromium = +3
Electronic configuration for \(d^{ 3} = t_{2g}^ 3 \)
Coordination number = 6
Shape: octahedral.
Stereochemistry:
Both isomers are optically active.
Therefore, a total of 4 isomers exist.
Magnetic moment\(, ÃŽÂ\frac{1}{4}=\sqrt{n(n+2)}\)
\(=\sqrt{3(3+2)}\)
\(=\sqrt{15}\)
∼ 4BM
\((iv) Cs[FeCl_4] \)
IUPAC name: Caesium tetrachloroferrate (III)
Oxidation state of\( Fe = +3\)
Electronic configuration of \(d ^{6} = eg^{ 2} t_{2g}^ 3 \)
Coordination number = 4 Shape: tetrahedral
Stereochemistry: optically inactive Magnetic moment: \(ÃŽÂ\frac{1}{4}=\sqrt{n(n+2)}\)
\(=\sqrt{5(5+2)}\)
\(=\sqrt{35}\)
~6BM
\((v) K_4[Mn(CN)_6]\) Potassium hexacyanomanganate(II)
Oxidation state of manganese=+2
Electronic configuration: \(d ^{5+}: t_{2g}^ 5 \)
Coordination number = 6 Shape: octahedral.
Streochemistry: optically inactive
Magnetic moment,\( ÃŽÂ\frac{1}{4}=\sqrt{n(n+2)}\)
\(=\sqrt{1(1+2)}\)
\(=\sqrt{3}\)
\(=1.732BM\)
The Crystal Field Theory (CFT) of coordination compounds is based on the effect of different crystal fields (provided by the ligands taken as point charges) on the degeneracy of d-orbital energies of the central metal atom/ion. The splitting of the d-orbitals provides different electronic arrangements in strong and weak crystal fields. In tetrahedral coordination entity formation, the d-orbital splitting is smaller as compared to the octahedral entity.
What is crystal field splitting energy?
The Crystal Field Theory (CFT) of coordination compounds is based on the effect of different crystal fields (provided by the ligands taken as point charges) on the degeneracy of d-orbital energies of the central metal atom/ion. The splitting of the d-orbitals provides different electronic arrangements in strong and weak crystal fields. In tetrahedral coordination entity formation, the d-orbital splitting is smaller as compared to the octahedral entity.
On the basis of CFT, explain why [Ti(H$_2$O)$_6$]Cl$_3$ complex is coloured? What happens on heating the complex [Ti(H$_2$O)$_6$]Cl$_3$? Give reason.
Nomenclature of Coordination Compounds is important in Coordination Chemistry because of the need to have an unambiguous method of describing formulas and writing systematic names, particularly when dealing with isomers.