The magnetic moment of a transition metal ion is due to the presence of **unpaired electrons** in its \( d \)-orbitals.
The **spin-only magnetic moment** is given by the formula: \[ \mu = \sqrt{n(n+2)} \, \text{BM} \] where \( n \) = number of unpaired electrons.
For \( \text{Mn}^{2+} \): Atomic number of Mn = 25 Electronic configuration of Mn = [Ar] 3d\(^5\) 4s\(^2\)
In \( \text{Mn}^{2+} \), two electrons are removed from the 4s orbital: \[ \text{Mn}^{2+} = [\text{Ar}] \, 3d^5 \]
Hence, the number of unpaired electrons \( n = 5 \).
Substituting in the formula: \[ \mu = \sqrt{5(5 + 2)} = \sqrt{35} = 5.916 \, \text{BM} \]
Therefore, the spin-only magnetic moment of \( \text{Mn}^{2+} \) ion is: \[ \boxed{5.916 \, \text{BM}} \]
The correct IUPAC name of \([ \text{Pt}(\text{NH}_3)_2\text{Cl}_2 ]^{2+} \) is:
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.