Dipotassium cyclooctatetraenide

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Dipotassium cyclooctatetraenide
Dipotassium cyclooctatetraenide.svg
Names
IUPAC name
dipotassium cycloocatetraenediide
Identifiers
3D model (JSmol)
ChemSpider
PubChem CID
Properties
C8H8K2
Appearancebeige solid
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Dipotassium cyclooctatetraenide, sometimes abbreviated K2COT, is an organopotassium compound with the formula K2C8H8. It is a brown solid that is used as a precursor to cyclooctatetraenide complexes, such as uranocene (U(C8H8)2). Analogs of K2C8H8 are known with ring substituents, with different alkali metals, and with various complexants.

Ball-and-stick model of COT Cyclooctatetraenide-3D-ball.png
Ball-and-stick model of COT

Preparation and structure

Potassium cyclooctatetraenide is formed by the reaction of cyclooctatetraene with potassium metal:

2 K + C8H8 → K2C8H8

The reaction entails 2-electron reduction of the polyene and is accompanied by a color change from colorless to brown. [1]

The structure of K2(diglyme)C8H8 has been characterized by X-ray crystallography of the derivatives with diglyme complexed to the potassium cations. The C8H8 unit is planar with an average C-C distance of 1.40 A. [2]

Related Research Articles

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5
H
5
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Cyclooctatetraene

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Cyclooctatetraenide anion

In chemistry, the cyclooctatetraenide anion or cyclooctatetraenide, more precisely cyclooctatetraenediide, is an aromatic species with a formula of [C8H8]2− and abbreviated as COT2−. It is the dianion of cyclooctatetraene. Salts of the cyclooctatetraenide anion can be stable, e.g., Dipotassium cyclooctatetraenide or disodium cyclooctatetraenide. More complex coordination compounds are known as cyclooctatetraenide complexes, such as the actinocenes.

Lithium diphenylphosphide

Lithium diphenylphosphide contains lithium and the organophosphorus anion with the formula (C6H5)2PLi. It is an air-sensitive solid that is used in the preparation of diphenylphosphino compounds. As an ether complex, the lithium salt is dark red.

References

  1. A. L Wayda (1990). "Cyclooctatetraene Lanthanide Complexes. Lu(C8H8Cl(thf) and Lu(C8H8)[o-C6H4CH2N(CH3)2(thf)". Inorganic Syntheses. 27: 150. doi:10.1002/9780470132586.ch28.
  2. J. H. Noordik, T. E. M. van den Hark, J. J. Mooij and A. A. K. Klaassen (1974). "Dipotassium(I) cyclooctatetraenide-1-methoxy-2-(2-methoxyethoxy)ethane". Acta Crystallogr B. 30 (30): 833–835. doi:10.1107/S0567740874003840.CS1 maint: multiple names: authors list (link)