Platinum(II) chloride
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Template:Chembox image cellTemplate:Chembox image cellTemplate:Chembox AllOtherNamesTemplate:Chembox headerbarTemplate:Chembox IndexlistTemplate:Chembox JmolTemplate:Chembox ChEMBLTemplate:Chembox ECHATemplate:Chembox E numberTemplate:Chembox IUPHAR ligandTemplate:Chembox UNIITemplate:Chembox CompToxTemplate:Chembox headerbarTemplate:Chembox SolubilityInWaterTemplate:Chembox headerbarTemplate:Chembox HazardsTemplate:Chembox headerbarTemplate:Chembox Datapage checkTemplate:Yesno| Template:Longitem | Template:Unbulleted list |
| ChEBI | Template:Unbulleted list |
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| EC Number | Template:Unbulleted list |
| Template:Longitem | 1744965 |
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| Template:Longitem | PtCl2 |
| Molar mass | 265.99 g/mol |
| Appearance | dark brown powder |
| Density | 6.05 g/cm3, solid |
| Melting point | Template:Chembox CalcTemperatures |
| Boiling point | Template:Chembox CalcTemperatures |
| Solubility | insoluble in alcohol, ether soluble in HCl, ammonia |
| Template:Longitem | −54.0·10−6 cm3/mol |
| Template:Longitem | hexagonal |
| Template:Longitem | Platinum(II) bromide Platinum(II) sulfide |
| Template:Longitem | Palladium(II) chloride |
| Template:Longitem | Platinum(IV) chloride |
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Platinum(II) chloride describes the inorganic compounds with the formula PtCl2. They are precursor used in the preparation of other platinum compounds. Platinum(II) chloride exists in two crystalline forms (polymorphs), but the main properties are somewhat similar: dark brown, insoluble in water, diamagnetic, and odorless.
Structure
The structures of PtCl2 and PdCl2 are similar. These dichlorides exist in both polymeric, or "α", and hexameric, or "β" structures. The β form converts to the α form at 500 °C. In the β form, the Pt-Pt distances are 3.32–3.40 Å, indicative of some bonding between the pairs of metals. In both forms of PtCl2, each Pt center is four-coordinate, being surrounded by four chloride ligands. Complementarily, each Cl center is two-coordinate, being connected to two platinum atoms.[1] The structure of α-PtCl2 is reported to be disordered and contain edge- and/or corner-sharing square-planar PtCl4 units.[2]
Preparation
β-PtCl2 is prepared by heating chloroplatinic acid to 350 °C in air.[3]
- H2PtCl6 → PtCl2 + Cl2 + 2 HCl
This method is convenient since the chloroplatinic acid is generated readily from Pt metal. Aqueous solutions of H2PtCl6 can also be reduced with hydrazinium salts, but this method is more laborious than the thermal route of Kerr and Schweizer.
Although PtCl2 can form when platinum metal contacts hot chlorine gas, this process suffers from over-chlorination to give PtCl4. Berzelius and later Wöhler and Streicher showed that upon heating to 450 °C, this Pt(IV) compound decomposes to the Pt(II) derivative:[4][5]
- PtCl4 → PtCl2 + Cl2
Transformations such as this are "driven" by entropy, the free energy gained upon the release of a gaseous product from a solid. Upon heating to still higher temperatures, PtCl2 releases more chlorine to give metallic Pt. This conversion is the basis of the gravimetric assay of the purity of the PtCl2 product.
Reactions
Most reactions of PtCl2 proceed via treatment with ligands (L) to give molecular derivatives. These transformations entail depolymerization via cleavage of Pt-Cl-Pt linkages:
- PtCl2 + 2 L → PtCl2L2
Addition of ammonia gives initially "PtCl2(NH3)2", "Magnus's green salt", also described as [Pt(NH3)4][PtCl4].
Many complexes have been described, the following are illustrative:[6]
- pink K2PtCl4, a widely employed water-soluble derivative.
- colorless cis-PtCl2(NH3)2, better known as cisplatin.
- colorless cis-PtCl2(P(C6H5)3)2, a common precursor to other complexes of the type PtX(Cl)(P(C6H5)3)2 (X = H, CH3, etc.).
- yellow trans-PtCl2(P(C6H5)3)2, a metastable relative of the cis- isomer.
- colorless dichloro(cycloocta-1,5-diene)platinum(II) (Pt(cod)Cl2), an "organic-soluble" compound containing a labile organic ligand.
Several of these compounds are of interest in homogeneous catalysis in the service of organic synthesis or as anti-cancer drugs.
See also
References
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- ↑ Holleman, A. F.; Wiberg, E. Inorganic Chemistry Academic Press: San Diego, 2001. Template:ISBN.
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- ↑ Cotton, S. A. Chemistry of Precious Metals, Chapman and Hall (London): 1997. Template:ISBN
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