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Dichloro(1,5-cyclooctadiene)platinum(II)
[CAS# 12080-32-9]

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Identification
Classification Organic raw materials >> Organometallic compound >> Organic hafnium, mercury, silver, platinum, etc.
Name Dichloro(1,5-cyclooctadiene)platinum(II)
Synonyms (1,5-Cyclooctadiene)platinum(II) dichloride; Platinum(COD)dichloride
Molecular Structure CAS # 12080-32-9, Dichloro(1,5-cyclooctadiene)platinum(II), (1,5-Cyclooctadiene)platinum(II) dichloride, Platinum(COD)dichloride
Molecular Formula C8H12Cl2Pt
Molecular Weight 374.16
CAS Registry Number 12080-32-9
EC Number 235-144-5
SMILES C1/C=C\CC/C=C\C1.Cl[Pt]Cl
Properties
Melting point 285 ºC (Decomposes) (Expl.)
Water solubility insoluble
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H315-H319-H335    Details
Precautionary Statements P261-P264-P264+P265-P271-P280-P302+P352-P304+P340-P305+P351+P338-P319-P321-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2H319
Specific target organ toxicity - single exposureSTOT SE3H335
Acute toxicityAcute Tox.4H302
Acute toxicityAcute Tox.4H312
Acute toxicityAcute Tox.4H332
Respiratory sensitizationResp. Sens.1H334
Flammable solidsFlam. Sol.2H228
Chronic hazardous to the aquatic environmentAquatic Chronic4H413
Skin sensitizationSkin Sens.1H317
SDS Available
up Discovory and Applicatios
Dichloro(1,5-cyclooctadiene)platinum(II) is a coordination complex with the formula PtCl2(COD), where COD stands for 1,5-cyclooctadiene (C8H12). It consists of a platinum(II) center coordinated by two chloride ligands and a bidentate 1,5-cyclooctadiene ligand, which binds through its two alkene groups. This compound appears as a yellow to orange crystalline solid and is soluble in common organic solvents such as dichloromethane and chloroform.

The compound was first synthesized during studies of platinum organometallic chemistry in the mid-20th century, when researchers explored complexes of platinum with unsaturated hydrocarbons. The use of cyclooctadiene as a ligand helped stabilize the platinum(II) center, enabling the isolation and characterization of a variety of platinum complexes. Structural determination by X-ray crystallography showed that the platinum center adopts a square planar geometry typical of d8 metal ions, with the COD ligand coordinating in a chelating fashion and the two chloride ligands completing the coordination sphere.

Dichloro(1,5-cyclooctadiene)platinum(II) is commonly prepared by reacting potassium tetrachloroplatinate(II) (K2PtCl4) with 1,5-cyclooctadiene under reflux conditions in an aqueous or organic medium. The reaction proceeds through ligand substitution, where two chloride ions are retained while the COD ligand binds to platinum, resulting in the discrete complex.

This complex is widely used as a versatile precursor in platinum-based organometallic synthesis and catalysis. Its relatively labile COD ligand can be displaced by other ligands such as phosphines, amines, or olefins, facilitating the preparation of a broad range of platinum complexes with tailored properties. Such complexes find applications in homogeneous catalysis, including hydrosilylation, hydrogenation, and carbon-carbon bond-forming reactions.

In addition, dichloro(1,5-cyclooctadiene)platinum(II) serves as a starting material for the synthesis of platinum-containing polymers, materials for electronics, and medicinal compounds. Its well-defined structure and solubility make it suitable for detailed mechanistic studies in organometallic chemistry.

Handling of this platinum complex requires caution due to the toxicity of platinum compounds and their potential environmental impact. It may cause skin and respiratory irritation, and prolonged exposure should be avoided. Proper personal protective equipment and ventilation are recommended during its use.

In summary, dichloro(1,5-cyclooctadiene)platinum(II) is a stable, square planar platinum(II) complex widely utilized as a synthetic precursor in organometallic chemistry and catalysis. Its coordination with the COD ligand enables easy ligand substitution, supporting diverse applications in synthesis and material science.

References

2024. Synthesis of a Novel Platinum Catalyst and Its Application in the Photoactivated Hydrosilylation Reaction. Silicon, 16(15).
DOI: 10.1007/s12633-024-03103-8

2020. Platinum Atoms Dispersed in Single-chain Polymer Nanoparticles. Chinese Journal of Polymer Science, 39(2).
DOI: 10.1007/s10118-021-2499-x

2011. A kinetic investigation into the rate of chloride substitution from chloro terpyridine platinum(II) and analogous complexes by a series of azole nucleophiles. Transition Metal Chemistry, 36(5).
DOI: 10.1007/s11243-011-9507-x
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