Tropylium cation

History

In 1891 G. Merling obtained a water-soluble bromine-containing compound from the reaction of cycloheptatriene and bromine. Unlike most alkyl bromides, this compound, later named tropylium bromide, is water-soluble but insoluble in many organic solvents. It is purified by crystallization from hot ethanol. Reaction with aqueous silver nitrate immediately gave silver bromide, indicating labile bromide. Tropylium bromide was deduced to be a salt, , by Doering and Knox in 1954 by analysis of its infrared and ultraviolet spectra. The ionic structures of tropylium perchlorate () and tropylium iodide () have been confirmed by X-ray crystallography. The bond length of the carbon-carbon bonds is longer (147 pm) than those of benzene (140 pm) but still shorter than those of a typical single-bonded species like ethane (154 pm).

Acidity

The tropylium ion is an acid in aqueous solution (i.e., an Arrhenius acid) as a consequence of its Lewis acidity: it first acts as a Lewis acid to form an adduct with water, which can then donate a proton to another molecule of water, therefore indirectly acting as an Arrhenius acid: : + 2 + (Boric acid gives acidic aqueous solutions in much the same way.) The equilibrium constant is , making it about as acidic in water as acetic acid.

Mass spectrometry

The tropylium ion is frequently encountered in mass spectrometry in the form of a signal at m/z = 91 and is used in mass spectrum analysis. This fragment is often found for aromatic compounds containing a benzyl unit. Upon ionization, the benzyl fragment forms a cation (), which rearranges to the highly stable tropylium cation ().

Reactions

The tropylium cation reacts with nucleophiles to form substituted cycloheptatrienes, for example: : + →

Reduction by lithium aluminium hydride yields cycloheptatriene.

Reaction with a cyclopentadienide salt of sodium or lithium yields 7-cyclopentadienylcyclohepta-1,3,5-triene: : + → +

When treated with oxidising agents such as chromic acid, the tropylium cation undergoes rearrangement into benzaldehyde:

: + → + +

Many metal complexes of tropylium ion are known. One example is [Mo(η7-C7H7)(CO)3]+, which is prepared by hydride abstraction from cycloheptatrienemolybdenum tricarbonyl.

References

de:Tropylium

References

1. "tropylium {{!}} ChemSpider".
2. [[International Union of Pure and Applied Chemistry]]. (2014). "Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013". [[Royal Society of Chemistry.
3. "Tropylium".
4. "molecule".
5. A mixture of [C₇H₇]⁺Cl⁻ and [C₇H₇]⁺[{{chem. PCl. 6. −] is produced by treatment of tropylidene with phosphorus pentachloride.
6. ''Tropylium fluoborate'' Organic Syntheses, Coll. Vol. 5, p.1138 (1973); Vol. 43, p.101 (1963). [http://orgsyn.org/orgsyn/pdfs/CV5P1138.pdf link] {{Webarchive. link. (2012-08-29)
7. Merling, G.. (1891). "Ueber Tropin". Berichte der Deutschen Chemischen Gesellschaft.
8. (1954). "The Cycloheptatrienylium (Tropylium) Ion". J. Am. Chem. Soc..
9. (2004). "Aromaticity as a Cornerstone of Heterocyclic Chemistry". Chem. Rev..
10. (1960). "Crystal structures of tropylium perchlorate and iodide". Bulletin of the Academy of Sciences of the USSR Division of Chemical Science.
11. (1994). "Tropylium Ion Formation from Toluene: Solution of an Old Problem in Organic Mass Spectrometry". Accounts of Chemical Research.
12. O. P. Agarwai. (2009). "Reactions and Reagents". Krishna Prakashan Media.
13. (1995). "Cycloheptatriene and -enyl Complexes of the Early Transition Metals". Chemical Reviews.