Methanium

Short description: Ion of carbon with five hydrogens

Methanium

"True" methanium, the metastable transitional state [CH
5]+

Fluxional methanium, [CH
3(H
2)]+

Names
IUPAC name

Methanium

Other names

carbonium (discouraged due to multiple definitions)[1]

Identifiers

3D model (JSmol)

* true methanium: Interactive image
* fluxional methanium: Interactive image

PubChem CID

* 21881157

InChI

* true methanium: InChI=1S/CH5/h1H5/q+1

Key: PXOFOHGGCICFQD-UHFFFAOYSA-N

* fluxional methanium: InChI=1S/CH5/c1-2/h2H,1H3/q+1

Key: AJLDAZFHECSILY-UHFFFAOYSA-N

SMILES

* true methanium: [C+H5]

* fluxional methanium: [CH3+].[HH]

Properties

Chemical formula

| CH+

Molar mass | 17.051 g·mol−1
Conjugate base | Methane
Structure

Molecular shape

| trigonal bipyramidal

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Infobox references

In chemistry, methanium is a complex positive ion with formula [[[Chemistry:Carbon|C]]H
5]+
(metastable transitional form, a carbon atom covalently bonded to five hydrogen atoms) or [CH
3(H
2)]+
(fluxional form, namely a molecule with one carbon atom covalently bonded to three hydrogen atoms and one dihydrogen molecule), bearing a +1 electric charge. It is a superacid and one of the onium ions, indeed the simplest carbonium ion.

It is highly unstable and highly reactive even upon having a complete octet, thus granting its superacidic properties.

Methanium can be produced in the laboratory as a rarefied gas or as a dilute species in superacids. It was prepared for the first time in 1950 and published in 1952 by Victor Talrose and his assistant Anna Konstantinovna Lyubimova.[2][3] It occurs as an intermediate species in chemical reactions.

The methanium ion is named after methane (CH
4), by analogy with the derivation of ammonium ion (NH+
4) from ammonia (NH
3).

## Contents

* 1 Structure
* 2 Preparation
* 3 Stability and reactions
* 4 See also
* 5 References

## Structure

Fluxional methanium can be visualised as a CH+
3 carbenium ion with a molecule of hydrogen interacting with the empty orbital in a 3-center-2-electron bond. The bonding electron pair in the H
2 molecule is shared between the two hydrogen and one carbon atoms making up the 3-center-2-electron bond.[4]

The two hydrogen atoms in the H
2 molecule can continuously exchange positions with the three hydrogen atoms in the CH+
3 ion (a conformation change called pseudorotation, specifically the Berry mechanism). The methanium ion is therefore considered a fluxional molecule. The energy barrier for the exchange is quite low and occurs even at very low temperatures.[5][6]

Infrared spectroscopy has been used to obtain information about the different conformations of the methanium ion.[7][8][9] The IR spectrum of plain methane has two C-H bands from symmetric and asymmetric stretching at around 3000 cm−1 and two bands around 1400 cm−1 from symmetrical and asymmetric bending vibrations. In the spectrum of CH+
5 three asymmetric stretching vibrations are present around 2800–3000 cm−1, a rocking vibration at 1300 cm−1, and a bending vibration at 1100 1300 cm−1.

## Preparation

Methanium can be prepared from methane by the action of very strong acids, such as fluoroantimonic acid (antimony pentafluoride SbF
5 in hydrogen fluoride HF).[10]

At about 270 Pa of pressure and ambient temperature, the methane ion CH+
4 will react with neutral methane to yield methanium and a methyl radical:[11]

CH+
4 \+ CH
4 → CH+
5 \+ CH

The methanium ion can also be made in the gas phase via the reaction of methane and an H+
ion (i.e. a proton).[citation needed]

4 \+ H+
(g) → CH+

## Stability and reactions

The cations obtained by reaction of methane with SbF
5 \+ HF, including methanium, are stabilized by interactions with the HF molecules.

At low pressures (around 1 mmHg) and ambient temperatures, methanium is unreactive towards neutral methane.[11]

## See also

* Methenium
* Ammonium
* Ethanium

## References

1. ↑ Chemistry, International Union of Pure and Applied (2009). "carbonium ion" (in en). IUPAC Compendium of Chemical Terminology. IUPAC. doi:10.1351/goldbook.C00839. ISBN 978-0-9678550-9-7. http://goldbook.iupac.org/C00839.html. Retrieved 27 November 2018.
2. ↑ V. L. Talrose and A. K. Lyubimova, Dokl. Akad. Nauk SSSR 86, 909-912 (1952) (In Russian: Тальрозе, В. Л., and А. К. Любимова. "Вторичные процессы в ионном источнике масс-спектрометра." ДАН СССР 86 (1952): 909-912)
3. ↑ Nikolaev, Eugene (1998). "Victor Talrose: an appreciation". Journal of Mass Spectrometry 33 (6): 499–501. doi:10.1002/(SICI)1096-9888(199806)33:6<499::AID-JMS684>3.0.CO;2-C. ISSN 1076-5174. Bibcode: 1998JMSp...33..499N.
4. ↑ Rasul, Golam; Prakash, G.K. Surya; Olah, George A. (2011). "Comparative study of the hypercoordinate carbonium ions and their boron analogs: A challenge for spectroscopists". Chemical Physics Letters 517 (1–3): 1–8. doi:10.1016/j.cplett.2011.10.020. Bibcode: 2011CPL...517....1R.
5. ↑ Schreiner, Peter R.; Kim, Seung-Joon; Schaefer, Henry F.; von Ragué Schleyer, Paul (1993). "CH+5: The never‐ending story or the final word?". Journal of Chemical Physics 99 (5): 3716–3720. doi:10.1063/1.466147.CH+5:+The+never‐ending+story+or+the+final+word?&rft.jtitle=Journal+of+Chemical+Physics&rft.aulast=Schreiner&rft.aufirst=Peter+R.&rft.au=Schreiner, Peter+R.&rft.au=Kim, Seung-Joon&rft.au=Schaefer, Henry+F.&rft.au=von+Ragué+Schleyer, Paul&rft.date=1993&rft.volume=99&rft.issue=5&rft.pages=3716–3720&rft_id=info:doi/10.1063/1.466147&rfr_id=info:sid/en.wikibooks.org:Chemistry:Methanium">
6. ↑ Müller, Hendrik; Kutzelnigg, Werner; Noga, Jozef; Klopper, Wim (1997). "CH5+: The story goes on. An explicitly correlated coupled-cluster study". Journal of Chemical Physics 106 (5): 1863. doi:10.1063/1.473340. Bibcode: 1997JChPh.106.1863M.
7. ↑ White, Edmund T.; Tang, Jian; Oka, Takeshi (1999). "CH+5: The infrared spectrum observed". Science 284 (5411): 135–7. doi:10.1126/science.284.5411.135. PMID 10102811. Bibcode: 1999Sci...284..135W.CH+5:+The+infrared+spectrum+observed&rft.jtitle=Science&rft.aulast=White&rft.aufirst=Edmund+T.&rft.au=White, Edmund+T.&rft.au=Tang, Jian&rft.au=Oka, Takeshi&rft.date=1999&rft.volume=284&rft.issue=5411&rft.pages=135–7&rft_id=info:doi/10.1126/science.284.5411.135&rft_id=info:pmid/10102811&rft_id=info:bibcode/1999Sci...284..135W&rfr_id=info:sid/en.wikibooks.org:Chemistry:Methanium">
8. ↑ Oskar Asvany, Padma Kumar P; Redlich, Britta; Hegemann, Ilka; Schlemmer, Stephan; Marx, Dominik (2005). "Understanding the infrared spectrum of bare CH+5.". Science 309 (5738): 1219–1222. doi:10.1126/science.1113729. PMID 15994376. Bibcode: 2005Sci...309.1219A.CH+5.&rft.jtitle=Science&rft.aulast=Oskar+Asvany&rft.aufirst=Padma+Kumar+P&rft.au=Oskar+Asvany, Padma+Kumar+P&rft.au=Redlich, Britta&rft.au=Hegemann, Ilka&rft.au=Schlemmer, Stephan&rft.au=Marx, Dominik&rft.date=2005&rft.volume=309&rft.issue=5738&rft.pages=1219–1222&rft_id=info:doi/10.1126/science.1113729&rft_id=info:pmid/15994376&rft_id=info:bibcode/2005Sci...309.1219A&rfr_id=info:sid/en.wikibooks.org:Chemistry:Methanium">
9. ↑ Huang, Xinchuan; McCoy, Anne B.; Bowman, Joel M.; Johnson, Lindsay M.; Savage, Chandra; Dong, Feng; Nesbitt, David J. (2006). "Quantum deconstruction of the infrared spectrum of CH+5.". Science 311 (5757): 60–63. doi:10.1126/science.1121166. PMID 16400143. Bibcode: 2006Sci...311...60H. https://zenodo.org/record/1230864.CH+5.&rft.jtitle=Science&rft.aulast=Huang&rft.aufirst=Xinchuan&rft.au=Huang, Xinchuan&rft.au=McCoy, Anne+B.&rft.au=Bowman, Joel+M.&rft.au=Johnson, Lindsay+M.&rft.au=Savage, Chandra&rft.au=Dong, Feng&rft.au=Nesbitt, David+J.&rft.date=2006&rft.volume=311&rft.issue=5757&rft.pages=60–63&rft_id=info:doi/10.1126/science.1121166&rft_id=info:pmid/16400143&rft_id=info:bibcode/2006Sci...311...60H&rft_id=https://zenodo.org/record/1230864&rfr_id=info:sid/en.wikibooks.org:Chemistry:Methanium">
10. ↑ Sommer, J.; Jost, R. (2000). "Carbenium and carbonium ions in liquid- and solid-superacid-catalyzed activation of small alkanes". Pure and Applied Chemistry 72 (12): 2309–2318. doi:10.1351/pac200072122309. http://195.37.231.82/publications/pac/pdf/2000/pdf/7212x2309.pdf.
11. ↑ 11.0 11.1 Field, F. H.; Munson, M. S. B. (1965). "Reactions of gaseous ions. XIV. Mass spectrometric studies of methane at pressures to 2 Torr". Journal of the American Chemical Society 87 (15): 3289–3294. doi:10.1021/ja01093a001.

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