Step 1: Basic idea.
According to Valence Bond Theory (VBT), the central metal ion in a coordination compound makes available a certain number of vacant orbitals (hybrid orbitals) for the formation of coordinate covalent bonds with ligands.
The ligands donate lone pairs of electrons into these vacant orbitals.
Step 2: Hybridisation concept.
- The type of hybridisation depends on the coordination number of the complex.
- For example:
- Coordination number 6 $\Rightarrow$ octahedral complexes $\Rightarrow$ \(d^2sp^3\) (inner orbital) or \(sp^3d^2\) (outer orbital).
- Coordination number 4 $\Rightarrow$ tetrahedral complexes $\Rightarrow$ \(sp^3\).
- Coordination number 4 $\Rightarrow$ square planar complexes $\Rightarrow$ \(dsp^2\).
Step 3: Example.
\([Co(NH_3)_6]^{3+}\): Cobalt in +3 oxidation state has 3d$^6$.
Pairing occurs to give empty \(d\)-orbitals.
Hybridisation is \(d^2sp^3\), leading to an octahedral geometry.
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\boxed{\text{VBT explains geometry, magnetic properties and bonding in coordination complexes.}}
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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.