Platinum(II) chloride

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Platinum(II) chloride
Ball-and-stick model of a Pt6Cl12 molecule in the beta polymorph of platinum(II) chloride
Names
IUPAC name
Platinum(II) chloride
Other names
Platinous chloride
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.030.019 Edit this at Wikidata
EC Number
  • 233-034-1
1744965
UNII
  • InChI=1S/2ClH.Pt/h2*1H;/q;;+2/p-2 checkY
    Key: CLSUSRZJUQMOHH-UHFFFAOYSA-L checkY
  • InChI=1/2ClH.Pt/h2*1H;/q;;+2/p-2
    Key: CLSUSRZJUQMOHH-NUQVWONBAP
  • monomer: Cl[Pt]Cl
  • hexamer: [Cl+]0[Pt-2]12[Cl+][Pt-2]34[Cl+][Pt-2]05[Cl+][Pt-2]6([Cl+]1)[Cl+][Pt-2]([Cl+]2)([Cl+]3)[Cl+][Pt-2]([Cl+]4)([Cl+]5)[Cl+]6
Properties
PtCl2
Molar mass 265.99 g/mol
Appearance dark brown powder
Density 6.05 g/cm3, solid
Melting point 581 °C (1,078 °F; 854 K)
Boiling point decomposes
insoluble
Solubility insoluble in alcohol, ether
soluble in HCl, ammonia
−54.0·10−6 cm3/mol
Structure
hexagonal
Hazards
GHS labelling:[1]
GHS05: CorrosiveGHS07: Exclamation markGHS08: Health hazard
Danger
H314, H315, H317, H319, H334
P260, P261, P264, P272, P280, P285, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P304+P341, P305+P351+P338, P310, P321, P332+P313, P333+P313, P337+P313, P342+P311, P362, P363, P405, P501
Lethal dose or concentration (LD, LC):
3423 mg/kg (rat, oral)
Related compounds
Other anions
Platinum(II) bromide
Platinum(II) sulfide
Other cations
Palladium(II) chloride
Related compounds
Platinum(IV) chloride
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Platinum(II) chloride is the chemical compound PtCl2. It is an important precursor used in the preparation of other platinum compounds. It exists in two crystalline forms, 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.[2] The structure of α-PtCl2 is reported to be disordered and contain edge- and/or corner-sharing square-planar PtCl4 units.[3]

Evolution of β-PtCl2 structure: Start with cubic lattice, remove corner and centered lattice points, inscribe octahedron (red lines), label corners as X (twelve Cl centers) and face-centered atoms as M (six Pt(II) centers).

Preparation

β-PtCl2 is prepared by heating chloroplatinic acid to 350 °C in air.[4]

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 must 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:[5][6]

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:[7]

  • 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

  1. ^ "Platinum(II) chloride". pubchem.ncbi.nlm.nih.gov. Retrieved 27 December 2021.
  2. ^ Holleman, A. F.; Wiberg, E. Inorganic Chemistry Academic Press: San Diego, 2001. ISBN 0-12-352651-5.
  3. ^ Krebs, Bernt; Brendel, Claus; Schäfer, Harald (1988). "Neue Untersuchungen an α‐Platindichlorid Darstellung und Struktur". Z. Anorg. Allg. Chem. 561 (1): 119–131. doi:10.1002/zaac.19885610113.
  4. ^ Kerr, G. T.; Schweizer, A. E. (2007). "β-Platinum(II) Chloride". Inorganic Syntheses. Vol. 20. pp. 48–49. doi:10.1002/9780470132517.ch14. ISBN 978-0-470-13251-7. {{cite book}}: |journal= ignored (help)
  5. ^ Wöhler, L.; Streicher, S. (1913). "Über das Beständigkeitsgebiet von vier wasserfreien Platinchloriden, über die Flüchtigkeit des Metalls im Chlorgas und die Darstellung sauerstoff-freien Chlors". Chem. Ber. 46 (2): 1591–1597. doi:10.1002/cber.19130460252.
  6. ^ A. E. Schweizer; G. T. Kerr (1978). "Thermal decomposition of hexachloroplatinic acid". Inorganic Chemistry. 17 (8): 2326–2327. doi:10.1021/ic50186a067.
  7. ^ Cotton, S. A. Chemistry of Precious Metals, Chapman and Hall (London): 1997. ISBN 0-7514-0413-6