Zeise's salt

Zeise's salt[1]
Names
IUPAC name
Potassium trichloro(ethene)platinate(II) hydrate
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.158.770
EC Number
  • 630-445-1
  • InChI=1S/C2H4.3ClH.K.H2O.Pt/c1-2;;;;;;/h1-2H2;3*1H;;1H2;/q;;;;+1;;+2/p-3
    Key: DCEGWIMEFFONKJ-UHFFFAOYSA-K
  • [K+].C=C.Cl[Pt-](Cl)Cl.O
Properties
C2H6Cl3KOPt
Molar mass 386.60 g·mol−1
Appearance Yellow crystals
Melting point 220 °C
Hazards
GHS labelling:[2]
GHS07: Exclamation mark
Warning
H315, H319, H335
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Zeise's salt, potassium trichloro(ethylene)platinate(II) hydrate, is the chemical compound with the formula K[PtCl3(C2H4)]·H2O. The anion of this air-stable, yellow, coordination complex contains a ethylene as a ligand bound to the Pt. The salt is of historical importance in the area of organometallic chemistry as one of the first examples of a transition metal alkene complex and is named for its discoverer, William Christopher Zeise.[3]

Preparation

This compound was originally prepared by Zeise by heating mixtures of platinum chlorides and potassium chloride in ethanol. Under suitable conditions, the ethanol converts to sufficient ethylene to allow the formation of the salt.[3] The hydrate can be more readily prepared by treating a solution of K2[PtCl4] and ethylene with a catalytic amount of SnCl2. The water of hydration can be removed in vacuo.[4] Zeise's salt is commercially available as a hydrate.

Structure

The anion is the component of this salt that is of interest. In the anion Pt is bound to (or "coordinated to") four ligands: three chlorides (Cl-) and ethylene (C2H4). The PtCl3 group is nearly planar and bisects the C=C bond of the ethylene ligand, which is oriented in a perpendicular manner. Both carbons of the ethylene are bonded to Pt, an interaction described as η2.[5] The Pt-Cl bond trans to ethylene is 234 pm in length, while the other two Pt-Cl bonds are near 230 pm.[6] In Zeise's salt and related compounds, the alkene rotates about the metal-alkene bond with a modest activation energy. Analysis of the barrier heights indicates that the π-bonding between most metals and the alkene is weaker than the σ-bonding.

History

Zeise's salt was one of the first organometallic compounds to be reported.[7] It was discovered by William Christopher Zeise, a professor at the University of Copenhagen, who prepared this compound in 1830 while investigating the reaction of PtCl4 with boiling ethanol. Following careful analysis he proposed that the resulting compound contained ethylene. Justus von Liebig, a highly influential chemist of that era, often criticised Zeise's proposal, but Zeise's proposal was decisively supported in 1868 when Birnbaum prepared the complex using ethylene.[8] Zeise's salt received a great deal of attention during the second half of the 19th century because chemists could not explain its molecular structure. This question remained unanswered until the determination of its X-ray crystal structure in the 20th century.[9][10] Zeise's salt stimulated much scientific research in the field of organometallic chemistry and would be key in defining new concepts in chemistry.

Many other ethylene complexes have been prepared. For example, ethylenebis(triphenylphosphine)platinum(0), [(C6H5)3P]2Pt(H2C=CH2), wherein the platinum is three-coordinate and in oxidation state 0 (Zeise's salt is a derivative of platinum(II)).

References

  1. ^ Aldrich datasheet
  2. ^ "C&L Inventory". echa.europa.eu.
  3. ^ a b D. Seyferth (2001). "[(C2H4)PtCl3]-, the Anion of Zeise's Salt, K[(C2H4)PtCl3]·H2O". Organometallics. 20: 2–6. doi:10.1021/om000993+.
  4. ^ Chock, P. B.; Halpern, J.; Paulik, F. E. (1990). "Potassium Trichloro(Ethene)Platinate(II) (Zeise's Salt)". Inorganic Syntheses. 28: 349. doi:10.1002/9780470132593.ch90.
  5. ^ Black, M.; Mais, R. H. B.; Owston, P. G. (1969). "The crystal and molecular structure of Zeise's salt, KPtCl3·C2H4·H2O". Acta Crystallogr. B25 (9): 1753–1759. Bibcode:1969AcCrB..25.1753B. doi:10.1107/S0567740869004699.
  6. ^ Love, R. A.; Koetzle, T. F.; Williams, G. J. B.; Andrews, L. C.; Bau, R. (1975). "Neutron diffraction study of the structure of Zeise's salt, KPtCl3·C2H4·H2O". Inorg. Chem. 14 (11): 2653–2657. doi:10.1021/ic50153a012.
  7. ^ Zeise, W. C. (1831). "Von der Wirkung zwischen Platinchlorid und Alkohol, und von den dabei entstehenden neuen Substanzen" [On the reaction between platinum chloride and alcohol, and its resulting new substances]. Ann. Phys. Chem. (in German). 97 (4): 497–541. Bibcode:1831AnP....97..497Z. doi:10.1002/andp.18310970402.
  8. ^ Hunt, L. B. (1984). "The First Organometallic Compounds: William Christopher Zeise and His Platinum Complexes". Platin. Met. Rev. 28 (2): 76–83. doi:10.1595/003214084X2827683. S2CID 100304495. Archived from the original on 2023-05-22. Retrieved 2022-09-28.
  9. ^ Black, M.; Mais, R. H. B.; Owston, P. G. (1969). "The crystal and molecular structure of Zeise's salt, KPtCl3.C2H4.H2O". Acta Crystallogr. B. 25 (9): 1753–1759. Bibcode:1969AcCrB..25.1753B. doi:10.1107/S0567740869004699.
  10. ^ Jarvis, J. A. J.; Kilbourn, B. T.; Owston, P. G. (1971). "A Re-determination of the Crystal and Molecular Structure of Zeise's salt, KPtCl3.C2H4.H2O". Acta Crystallogr. B. 27 (2): 366–372. Bibcode:1971AcCrB..27..366J. doi:10.1107/S0567740871002231.
  11. ^ Steven D. Paget (2001). "(−)-Dichloro(ethylene)(α-methylbenzylamine)platinum(II)". Encyclopedia of Reagents for Organic Synthesis. John Wiley & Sons. doi:10.1002/047084289X.rd119. ISBN 0-471-93623-5.
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