Argonium

Argonium
Names
IUPAC name
Argonium ion
Other names
Hydridoargon(1+)
argon hydride cation[1]
protonated argon[2]
Identifiers
3D model (JSmol)
  • InChI=1S/ArH/h1H/q+1 checkY[NIST]
    Key: TVQSUVFYDVJWLI-UHFFFAOYSA-N checkY[NIST]
  • [ArH+]
Properties
ArH+
Molar mass 40.956 g·mol−1
Conjugate base Argon
Related compounds
Related compounds
 Helium hydride ion, Neonium, Kryptonium, Xenonium
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Argonium (also called the argon hydride cation, the hydridoargon(1+) ion, or protonated argon; chemical formula ArH+) is a cation combining a proton and an argon atom. It can be made in an electric discharge, and was the first noble gas molecular ion to be found in interstellar space.[3]

Properties

[edit]

Argonium is isoelectronic with hydrogen chloride. Its dipole moment is 2.18 D for the ground state.[4] The binding energy is 369 kJ mol−1[5] (3.9 eV[6]). This is smaller than that of H+
3 and many other protonated species, but more than that of H+
2.[5]

Rotationless radiative lifetimes of different vibrational states vary with isotope and become shorter for the more rapid high-energy vibrations:

Lifetimes (ms)[7]
v ArH+ ArD+
1 2.28 9.09
2 1.20 4.71
3 0.85 3.27
4 0.64 2.55
5 0.46 2.11

The force constant in the bond is calculated at 3.88 mdyne/Å2.[8]

Reactions

[edit]
  • ArH+ + H2 → Ar + H+
    3    [5]
  • ArH+ + C → Ar + CH+
  • ArH+ + N → Ar + NH+
  • ArH+ + O → Ar + OH+
  • ArH+ + CO → Ar + COH+[5]

But the reverse reaction happens:

  • Ar + H+
    2     → ArH+ + H.[5]
  • Ar + H+
    3     → *ArH+ + H2[5]

Ar+ + H2 has a cross section of 10−18 m2 for low energy. It has a steep drop off for energies over 100 eV[9] Ar + H+
2 has a cross sectional area of 6×10−19 m2 for low energy H+
2, but when the energy exceeds 10 eV yield reduces, and more Ar+ and H2 is produced instead.[9]

Ar + H+
3 has a maximum yield of ArH+ for energies between 0.75 and 1 eV with a cross section of 5×10−20 m2. 0.6 eV is needed to make the reaction proceed forward. Over 4 eV more Ar+ and H starts to appear.[9]

Argonium is also produced from Ar+ ions produced by cosmic rays and X-rays from neutral argon.

  • Ar+ + H2 → *ArH+ + H[5] 1.49 eV[6]

When ArH+ encounters an electron, dissociative recombination can occur, but it is extremely slow for lower energy electrons, allowing ArH+ to survive for a much longer time than many other similar protonated cations.

  • ArH+ + e− → Ar + H[5]

Because ionisation potential of argon atoms is lower than that of the hydrogen molecule (in contrast to that of helium or neon), the argon ion reacts with molecular hydrogen, but for helium and neon ions, they will strip an electron from a hydrogen molecule.[5]

  • Ar+ + H2 → ArH+ + H[5]
  • Ne+ + H2 → Ne + H+ + H (dissociative charge transfer)[5]
  • He+ + H2 → He + H+ + H[5]

Spectrum

[edit]

Artificial ArH+ made from earthly argon contains mostly the isotope 40Ar rather than the cosmically abundant 36Ar. Artificially it is made by an electric discharge through an argon–hydrogen mixture.[10] Brault and Davis were the first to detect the molecule using infrared spectroscopy to observe vibration–rotation bands.[10]

Far infrared spectrum of 40Ar1H+[10] 36Ar 38Ar[4]
Transition observed frequency
J GHz
1←0 615.8584 617.525 615.85815
2←1 1231.2712 1234.602
3←2 1845.7937
4←3 2458.9819
5←4 3080.3921
6←5 3679.5835
7←6 4286.1150
21←20 12258.483
22←21 12774.366
23←22 13281.119

The UV spectrum has two absorption points resulting in the ion breaking up. The 11.2 eV conversion to the B1Π state has a low dipole and so does not absorb much. A 15.8 eV to a repulsive A1Σ+ state is at a shorter wavelength than the Lyman limit, and so there are very few photons around to do this in space.[5]

Natural occurrence

[edit]

ArH+ occurs in interstellar diffuse atomic hydrogen gas. For argonium to form, the fraction of molecular hydrogen H2 must be in the range 0.0001 to 0.001. Different molecular ions form in correlation with different concentrations of H2. Argonium is detected by its absorption lines at 617.525 GHz (J = 1→0), and 1234.602 GHz (J = 2→1). These lines are due to the isotopolog 36Ar1H+ undergoing rotational transitions. The lines have been detected in the direction of the galactic centre SgrB2(M) and SgrB2(N), G34.26+0.15, W31C (G10.62−0.39), W49(N), and W51e, however where absorption lines are observed, argonium is not likely to be in the microwave source, but instead in the gas in front of it.[5] Emission lines are found in the Crab Nebula.[6]

In the Crab Nebula ArH+ occurs in several spots revealed by emission lines. The strongest place is in the Southern Filament. This is also the place with the strongest concentration of Ar+ and Ar2+ ions.[6] The column density of ArH+ in the Crab Nebula is between 1012 and 1013 atoms per square centimeter.[6] Possible the energy required to excite the ions so that then can emit comes from collisions with electrons or hydrogen molecules.[6] Towards the Milky Way centre the column density of ArH+ is around 2×1013 cm−2.[5]

Two isotopologs of argonium 36ArH+ and 38ArH+ are known to be in a distant unnamed galaxy with a redshift of z = 0.88582 (7.5 billion light years away) which is on the line of sight to the blazar PKS 1830−211.[4]

Electron neutralization and destruction of argonium outcompletes the formation rate in space if the H2 concentration is below 1 in 10−4.[11]

History

[edit]

Using the McMath solar Fourier transform spectrometer at Kitt Peak National Observatory, James W. Brault and Sumner P. Davis observed ArH+ vibration-rotation infrared lines for the first time.[12] J. W. C. Johns also observed the infrared spectrum.[13]

Use

[edit]

Argon facilitates the reaction of tritium (T2) with double bonds in fatty acids by forming an ArT+ (tritium argonium) intermediate.[14] When gold is sputtered with an argon-hydrogen plasma, the actual displacement of gold is done by ArH+.[15]

References

[edit]
  1. ^ NIST Computational Chemistry Comparison and Benchmark Database, NIST Standard Reference Database Number 101. Release 19, April 2018, Editor: Russell D. Johnson III. http://cccbdb.nist.gov/
  2. ^ Neufeld, David A.; Wolfire, Mark G. (2016). "The Chemistry of Interstellar Argonium and Other Probes of the Molecular Fraction in Diffuse Clouds". The Astrophysical Journal. 826 (2): 183. arXiv:1607.00375. Bibcode:2016ApJ...826..183N. doi:10.3847/0004-637X/826/2/183. S2CID 118493563.
  3. ^ Quenqua, Douglas (13 December 2013). "Noble Molecules Found in Space". The New York Times. Retrieved 26 September 2016.
  4. ^ a b c Müller, Holger S. P.; Muller, Sébastien; Schilke, Peter; Bergin, Edwin A.; Black, John H.; Gerin, Maryvonne; Lis, Dariusz C.; Neufeld, David A.; Suri, Sümeyye (7 October 2015). "Detection of extragalactic argonium, ArH+, toward PKS 1830−211". Astronomy & Astrophysics. 582: L4. arXiv:1509.06917. Bibcode:2015A&A...582L...4M. doi:10.1051/0004-6361/201527254. S2CID 10017142.
  5. ^ a b c d e f g h i j k l m n o Schilke, P.; Neufeld, D. A.; Müller, H. S. P.; Comito, C.; Bergin, E. A.; Lis, D. C.; Gerin, M.; Black, J. H.; Wolfire, M.; Indriolo, N.; Pearson, J. C.; Menten, K. M.; Winkel, B.; Sánchez-Monge, Á.; Möller, T.; Godard, B.; Falgarone, E. (4 June 2014). "Ubiquitous argonium (ArH+) in the diffuse interstellar medium: A molecular tracer of almost purely atomic gas". Astronomy & Astrophysics. 566: A29. arXiv:1403.7902. Bibcode:2014A&A...566A..29S. doi:10.1051/0004-6361/201423727. S2CID 44021593.
  6. ^ a b c d e f Barlow, M. J.; Swinyard, B. M.; Owen, P. J.; Cernicharo, J.; Gomez, H. L.; Ivison, R. J.; Krause, O.; Lim, T. L.; Matsuura, M.; Miller, S.; Olofsson, G.; Polehampton, E. T. (12 December 2013). "Detection of a Noble Gas Molecular Ion, 36ArH+, in the Crab Nebula". Science. 342 (6164): 1343–1345. arXiv:1312.4843. Bibcode:2013Sci...342.1343B. doi:10.1126/science.1243582. PMID 24337290. S2CID 37578581.
  7. ^ Pavel Rosmus (1979). "Molecular Constants for the 1Σ+ Ground State of the ArH+ Ion". Theoretica Chimica Acta. 51 (4): 359–363. doi:10.1007/BF00548944. S2CID 98475430.
  8. ^ Fortenberry, Ryan C. (June 2016). "Quantum astrochemical spectroscopy". International Journal of Quantum Chemistry. 117 (2): 81–91. doi:10.1002/qua.25180.
  9. ^ a b c Phelps, A. V. (1992). "Collisions of H+, H+
    2    , H+
    3    , ArH+, H−, H, and H2 with Ar and of Ar+ and ArH+ with H2 for Energies from 0.1 eV to 10 keV". J. Phys. Chem. Ref. Data. 21 (4). doi:10.1063/1.555917.
  10. ^ a b c Brown, John M.; Jennings, D.A.; Vanek, M.; Zink, L.R.; Evenson, K.M. (April 1988). "The pure rotational spectrum of ArH+". Journal of Molecular Spectroscopy. 128 (2): 587–589. Bibcode:1988JMoSp.128..587B. doi:10.1016/0022-2852(88)90173-7.
  11. ^ David A. Neufeld; Mark G. Wolfire (1 July 2016). "The chemistry of interstellar argonium and other probes of the molecular fraction in diffuse clouds". The Astrophysical Journal. 826 (2): 183. arXiv:1607.00375. Bibcode:2016ApJ...826..183N. doi:10.3847/0004-637X/826/2/183. S2CID 118493563.
  12. ^ Brault, James W; Davis, Sumner P (1 February 1982). "Fundamental Vibration-Rotation Bands and Molecular Constants for the ArH+ Ground State (1Σ+ )". Physica Scripta. 25 (2): 268–271. Bibcode:1982PhyS...25..268B. doi:10.1088/0031-8949/25/2/004. S2CID 250825672.
  13. ^ Johns, J.W.C. (July 1984). "Spectra of the protonated rare gases". Journal of Molecular Spectroscopy. 106 (1): 124–133. Bibcode:1984JMoSp.106..124J. doi:10.1016/0022-2852(84)90087-0.
  14. ^ Peng, C. T. (April 1966). "Mechanism of Addition of Tritium to Oleate by Exposure to Tritium Gas". The Journal of Physical Chemistry. 70 (4): 1297–1304. doi:10.1021/j100876a053. PMID 5916501.
  15. ^ Jiménez-Redondo, Miguel; Cueto, Maite; Doménech, José Luis; Tanarro, Isabel; Herrero, Víctor J. (3 November 2014). "Ion kinetics in Ar/H2 cold plasmas: the relevance of ArH+" (PDF). RSC Advances. 4 (107): 62030–62041. Bibcode:2014RSCAd...462030J. doi:10.1039/C4RA13102A. ISSN 2046-2069. PMC 4685740. PMID 26702354.
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