Ethenium

Ethenium (C
2
H+
5
)

In chemistry, ethenium or protonated ethylene is a positive ion with formula C
2
H+
5
. It can be viewed as a molecule of ethylene C
2
H
4
with an added proton H+
, or a molecule of ethane minus an hydride ion H
. It is a carbocation; more specifically, a carbenium ion.

Preparation

Ethenium has been observed in rarefied gases subjected to radiation.[1] Another preparation method is the reaction of certain proton donors such as H+
3
, HeH+
, N
2
H+
, and N
2
OH+
with ethane at ambient temperature and pressures below 1 mmHg. (Other donors such as CH+
5
and HCO+
will form ethanium preferably to ethenium.)[2]

At room temperature and in a rarefied methane atmosphere, ethanium slowly dissociates to ethenium and H
2
. The reaction is much faster at 90 °C.[1]

Stability and reactions

Contrary to some earlier reports, ethenium was found to be largely unreactive towards neutral methane at ambient temperature and low pressure (on the order of 1 mmHg), even though the reaction yielding sec-C
3
H+
7
and H
2
is believed to be exothermic.[3]

Structure

The structure of ethenium's ground state was in dispute for many years, but it was eventually agreed to be a non-classical structure, with the two carbon atoms and one of the hydrogen atoms forming a three-center two-electron bond.

References

  1. 1.0 1.1

[1]

[2]

[3]

  1. Margaret French and Paul Kebarle (1975), "Pyrolysis of C
    2
    H+
    7
    and other ion-molecule reactions in methane containing traces of ethane". Canadian Journal of Chemistry, volume 53, pages 2268-2274. doi:10.1139/v75-318
  2. G. I. Mackay, H. I. Schiff, D. K. Bohme (1981), "A room-temperature study of the kinetics and energetics for the protonation of ethane" Canadian Journal of Chemistry, volume 59, issue 12,pages 1771-1778. doi:10.1139/v81-265
  3. F. H. Field , M. S. B. Munson (1965), "Reactions of gaseous ions. XIV. Mass spectrometric studies of methane at pressures to 2 Torr". Journal of the American Chemical Society, volume 87, issue 15, pages 3289–3294 doi:10.1021/ja01093a001
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