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==Stability and reactions==
==Stability and reactions==
In rarefied atmospheres at 30 [[celsius|C]], ethanium dissociates very slowly to ethenium and {{chem|H|2}}; the decomposition is considerably faster at 92 C.<ref name=French/> <ref name=Mackay/>
At about 1 mmHg and 30 [[celsius|C]], ethanium dissociates very slowly to ethenium and {{chem|H|2}}, across an energy barrier of about 10 [[kilocalorie|kcal]]/[[mole|mol]]; the decomposition is considerably faster at 92 C.<ref name=French/> <ref name=Mackay/>


==Structure==
==Structure==
Like its "unsaturated" relatives ethenium and [[ethynium]] {{chem|C|2|H|3|+}}, the ethanium ion was conjectured to have (at least momentarily) a proton bound simultaneously to the two [[carbon]] atoms, and the electrical charge evenly spread between them, as in other [[non-classical ion]]s. The alternative "classical" structure would have the charge and the extra hydrogen bound to only one of the two atoms, i.e. a [[methyl group|methyl]]ated methanium ion.
Like its "unsaturated" relatives ethenium and [[ethynium]] {{chem|C|2|H|3|+}}, the ethanium ion was conjectured to have (at least momentarily) a proton bound simultaneously to the two [[carbon]] atoms, and the electrical charge evenly spread between them, as in other [[non-classical ion]]s. The alternative "classical" structure would have the charge and the extra hydrogen bound to only one of the two atoms, i.e. a [[methyl group|methyl]]ated methanium ion.


Earlier calculations had predicted that the energies of the two forms should be 4 to 12 [[kilocalorie|kcal]]/[[mole|mol]] lower than the dissociated state {{chem|C|2|H|5|+}} + {{chem|H|2}}, and they should be separated by a slightly positive energy barrier.<ref name=yeh/> Gas-phase [[infrared spectroscopy]] has shown that both forms are stable.<ref name=yeh/> The bridged structure has the lowest [[energy]], 4 to 8 [[kilocalorie|kcal]]/[[mole|mol]] lower than the classical one.<ref name=yeh/>
Earlier calculations had predicted that the energies of the two forms should be 4 to 12 [[kilocalorie|kcal]]/[[mole|mol]] lower than the dissociated state {{chem|C|2|H|5|+}} + {{chem|H|2}}, and they should be separated by a slightly positive energy barrier.<ref name=yeh/> Gas-phase [[infrared spectroscopy]] by Yeh and others (1989) has shown that both forms are stable.<ref name=yeh/> The bridged structure has the lowest [[energy]], 4 to 8 [[kilocalorie|kcal]]/[[mole|mol]] lower than the classical one.<ref name=yeh/>

Refined calculations by Obata and Hirao (1993) predict that the most stable form has three orthogonal planes of symmetry (C<sub>2''v''</sub>) with the two {{chem|C|H|3}} subgroups in the [[eclipsed configuration]] (unlike ethane, whose ground state has the [[staggered configuration]]). Four "bottom" H atoms lie on a plane opposite to the bridging H atom and the other two "top" H atoms. The approximate computed distances are C–C 0.211 [[nanometre|nm]], C–H 0.124 nm (bridging), 0.107 nm (bottom) and 0.108 nm (top); the C–H–C angle at the bridge is about 116 degrees, the H–C–H angles are 116 degrees (bottom-bottom) and 114 degrees (bottom-top). However there are other configurations with near-minimum energy, including one where the two {{chem|C|H|3}} subgroups are slightly staggered (with C<sub>''s''</sub> symmetry), an another where one of the carbons of a {{chem|C|2|H|5|+}} ion is loosely bound to an {{chem|H|2}} molecule 0.250 nm away.<ref name=Obata/>


==References==
==References==
<references>
<references>

<ref name=Obata>
Shigeki Obata and Kimihiko Hirao (1993), "Structure and Vibrational Analysis of Protonated Ethane C2H7+", Bulletin of the Chemical Society of Japan
volume 66, issue 11, pages 3271-3282 {{doi|10.1246/bcsj.66.3271}}
</ref>


<ref name=Mackay>
<ref name=Mackay>

Revision as of 20:36, 21 February 2013

Ethanium (C
2
H+
7
)

In chemistry, ethanium or protonated ethane is a positive ion with formula C
2
H+
7
. It can be described as a molecule of ethane (C
2
H
6
) with one extra hydrogen atom and a +1 electric charge.

Ethanium is one of the simplest carbonium ions (after methanium CH+
5
). It was first detected as a rarefied gas in 1960 by S. Wexler and N. Jesse.[1] It easily dissociates into ethenium C
2
H+
5
and molecular hydrogen H
2
.

Production

Ethanium was first detected by infrared spectroscopy among the ions produced by electrical discharges in rarefied methane or ethane gas.[1]

Ethanium can also be produced by irradiating methane containing traces of ethane with an electron beam at low pressure (about 2 mmHg).[2] The electron beam first creates methanium and methenium ions. The former rapidly transfer their proton to ethane:

CH+
5
+ C
2
H
6
CH
4
+ C
2
H+
7

The latter reaction is also observed when CH+
5
, N
2
OH+
or HCO+
ions are injected into ethane at somewhat lowere pressure.[3]

Stability and reactions

At about 1 mmHg and 30 C, ethanium dissociates very slowly to ethenium and H
2
, across an energy barrier of about 10 kcal/mol; the decomposition is considerably faster at 92 C.[2] [3]

Structure

Like its "unsaturated" relatives ethenium and ethynium C
2
H+
3
, the ethanium ion was conjectured to have (at least momentarily) a proton bound simultaneously to the two carbon atoms, and the electrical charge evenly spread between them, as in other non-classical ions. The alternative "classical" structure would have the charge and the extra hydrogen bound to only one of the two atoms, i.e. a methylated methanium ion.

Earlier calculations had predicted that the energies of the two forms should be 4 to 12 kcal/mol lower than the dissociated state C
2
H+
5
+ H
2
, and they should be separated by a slightly positive energy barrier.[1] Gas-phase infrared spectroscopy by Yeh and others (1989) has shown that both forms are stable.[1] The bridged structure has the lowest energy, 4 to 8 kcal/mol lower than the classical one.[1]

Refined calculations by Obata and Hirao (1993) predict that the most stable form has three orthogonal planes of symmetry (C2v) with the two CH
3
subgroups in the eclipsed configuration (unlike ethane, whose ground state has the staggered configuration). Four "bottom" H atoms lie on a plane opposite to the bridging H atom and the other two "top" H atoms. The approximate computed distances are C–C 0.211 nm, C–H 0.124 nm (bridging), 0.107 nm (bottom) and 0.108 nm (top); the C–H–C angle at the bridge is about 116 degrees, the H–C–H angles are 116 degrees (bottom-bottom) and 114 degrees (bottom-top). However there are other configurations with near-minimum energy, including one where the two CH
3
subgroups are slightly staggered (with Cs symmetry), an another where one of the carbons of a C
2
H+
5
ion is loosely bound to an H
2
molecule 0.250 nm away.[4]

References

  1. ^ a b c d e L. I. Yeh, J. M. Price, and Y. T. Lee (1989), "Infrared spectroscopy of the pentacoordinated carbonium ion C
    2
    H+
    7
    ". Journal of the American Chemical Society, volume 111, pages 5591-5604. doi:10.1021/ja00197a015
  2. ^ a b 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
  3. ^ a b 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
  4. ^ Shigeki Obata and Kimihiko Hirao (1993), "Structure and Vibrational Analysis of Protonated Ethane C2H7+", Bulletin of the Chemical Society of Japan volume 66, issue 11, pages 3271-3282 doi:10.1246/bcsj.66.3271