Valence Bond Theory (VBT):
- VBT explains the bonding in coordination compounds by considering the hybridization of orbitals on the central metal atom or ion.
- The metal ion provides vacant orbitals to accommodate the lone pairs of electrons donated by ligands, forming coordinate covalent bonds.
- The geometry of the complex depends on the type of hybridization:
- \( sp^3 \): Tetrahedral
- \( dsp^2 \): Square planar
- \( d^2sp^3 \): Octahedral
Demerits of VBT:
1. Fails to explain the color of coordination compounds.
2. Cannot account for the magnetic properties of some complexes.
3. Does not provide a quantitative measure of bond strength or stability.
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.
Find the values of \( x, y, z \) if the matrix \( A \) satisfies the equation \( A^T A = I \), where
\[ A = \begin{bmatrix} 0 & 2y & z \\ x & y & -z \\ x & -y & z \end{bmatrix} \]