The given name is Tetraamminedibromoplatinum(IV) bromide.
Step 1: Identify the ligands and metal oxidation state.
- “Tetraammine” → 4 \( \text{NH}_3 \) ligands (neutral).
- “Dibromo” → 2 \( \text{Br}^- \) ligands (inside the coordination sphere).
- “Platinum(IV)” → Metal oxidation state = +4.
- “Bromide” (at the end of the name) → counter anion(s) outside the coordination sphere.
Step 2: Write the partial complex formula: \[ [\text{PtBr}_2(\text{NH}_3)_4]^{?} \]
Step 3: Determine the charge on the complex ion. Let the overall charge on the coordination sphere be \( x \). \[ x + (2 \times -1) + (4 \times 0) = +4 \] \[ x - 2 = +4 \implies x = +6 \] This would be incorrect since Pt(IV) rarely forms +6 complexes. Let’s reconsider the ligand count relative to oxidation state.
In the complex \( [\text{PtBr}_2(\text{NH}_3)_4] \), platinum has oxidation number: \[ x + (2 \times -1) = +4 \implies x = +6 \] Wait — correction: for a **Pt(IV)** ion, the total oxidation number is +4. So, \[ +4 = x + (-2) \implies x = +6 \] That means two bromides inside (each -1) give the total +4 charge for platinum. The coordination sphere has a net charge of +2.
Therefore, to balance the charge, there must be **two bromide ions** outside the coordination sphere. \[ [\text{PtBr}_2(\text{NH}_3)_4]\text{Br}_2 \]
Hence, the correct formula is: \[ \boxed{[\text{PtBr}_2(\text{NH}_3)_4]\text{Br}_2} \]
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.