Tetranitrogen

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Tetranitrogen
N4-C2-T.png
Names
IUPAC name
tetranitrogen
Identifiers
3D model (JSmol)
ChemSpider
PubChem CID
  • Tetrazete:InChI=1S/N4/c1-2-4-3-1
    Key: SSOWKQVDUZHCLS-UHFFFAOYSA-N
  • tetrahedral:InChI=1S/N4/c1-2-3(1)4(1)2
    Key: LVXZGECMVPLXCK-UHFFFAOYSA-N
  • Tetrazete:N1=NN=N1
  • tetrahedral:N12N3N1N23
Properties
N4
Molar mass 56.0268
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Tetranitrogen is a neutrally charged polynitrogen allotrope of the chemical formula N
4 and consists of four nitrogen atoms. The tetranitrogen cation is the positively charged ion, N+
4, which is more stable than the neutral tetranitrogen molecule and is thus more studied.

Contents

History

Polynitrogen compounds have been well known and characterized by chemists for many years. The commonplace molecular (diatomic) nitrogen (N
2) was first isolated by Daniel Rutherford in 1772 [1] and the azide ion (N−
3) was discovered by Theodor Curtius in 1890. [2] Discoveries of other related nitrogenous allotypes during the twentieth century include the aromatic molecule pentazole and the radical molecule N•
3. However, none of these complexes could be isolated or synthesized on a macroscopic scale like N
2 and azide; it was not until 1999 that a large scale synthesis was devised for a third nitrogen allotrope, the pentazenium (N+
5) cation. [3] This increased interest in polynitrogen compounds in the late twentieth century was due to the advance of computational chemistry which predicted that these types of molecules could be used as potential high-energy-density matter (HEDM) sources. [4]

The N+
4 cation was first discovered in 1958 upon analysis of anomalous background peaks of molecular weight 56+ and 42+ in the mass spectra of molecular nitrogen, which corresponded with formation of N+
4 and N+
3, respectively. [5] Explicit synthesis of N+
4 was first carried out in 1984 by a similar mechanism of electron bombardment of N
2. [6] Theoretical chemistry predicted several possible synthesis mechanisms for N
4 including reaction of a neutral N atom with a N•
3 radical, binding of two N
2 molecules in the excited state, and extrusion from polycyclic compounds, none of which could be accomplished experimentally. However, in 2002 a method for synthesis of tetranitrogen was devised from the deionization of N+
4 through neutralization-reionization mass spectrometry (NRMS). [7] In the synthesis, N+
4 (which was first formed in the ionization chamber of the mass spectrometer) underwent two high energy collision events. During the first collision, N+
4 contacted a target gas, CH
4, to yield a small percentage of neutral N
4 molecules. [7]

N+
4 + CH
4 → N
4 + CH+
4

A deflecting electrode was used to remove any unreacted N+
4 ions as well as the target gas, CH
4, and any additional unintended reaction products, leaving a stream of N
4 molecules. In order to affirm the synthesis and isolation of N
4, this stream then underwent a second collision event, contacting a second target gas, O
2, reforming the N+
4 cation. [7]

N
4 + O
2 → N+
4 + O−
2

The disappearance and reemergence of this "recovery peak" confirms the completion of both reactions, providing ample evidence for the synthesis of N
4 by this method. Because the "flight time" between the two reactions, carried out in separate chambers of the mass spectrometer, was on the order of 1  μs, the N
4 molecule has a lifetime of at least this long. [7]

Characteristics

Since its discovery, N
4 has not been well studied. It is a gas at room temperature (298 K, 25 °C, 77 °F). It also has a lifetime in excess of 1 μs, though it is predicted to be characterized as metastable. [7] Due to its instability, the N4 molecule readily disassociates into two more-stable N2 molecules. This process is very exothermic, releasing around 800 kJ mol−1 of energy. [7]

Ab initio calculations in the neutral molecular suggest that previously proposed rectangular or tetrahedral structures, analogous to cyclobutadiene and tetrahedrane, respectively, are not likely to be the most thermodynamically stable. Instead, the ground state is expected to be a bent or zig-zag linear chain of the four nitrogen atoms containing two unpaired electrons on one of the terminal nitrogen atoms—essentially an azido-nitrene. [8]

The structure of N+
4 has been predicted by theoretical experiments and confirmed by experimental techniques involving collisionally activated dissociation mass spectrometry (CADMS). This technique bombards N+
4-producing fragments which can then be analyzed by tandem mass spectrometry. Based on the fragments observed, a structure was determined invlvolving two pairs of triple-bonded nitrogen atoms (two N
2 units) that are associated with each other with a longer, weaker bond.

Applications

Tetranitrogen and other similar polynitrogen compounds are predicted to be good candidates for use as high-energy-density matter (HEDM), high energy fuel sources with small weight in comparison with traditional liquid and fuel cell-based energy sources. [9] [8] The N≡N triple bond of N
2 is much stronger (energy of formation of 229  kcal/mol) than either an equivalent one and a half N=N double bonds (100 kcal/mol, i.e. 150 kcal/mol total) or an equivalent three N−N single bonds (38.4 kcal/mol, i.e. 115 kcal/mol total). Because of this, polynitrogen molecules are expected to readily break down into harmless N
2 gas, in the process releasing large amounts of chemical energy. This is in contrast to carbon containing compounds which have lower energies of formation for an equivalent number of single or double bonds than for a C≡C triple bond, allowing for the thermodynamically favorable formation of polymers. [9] It is for this reason that the only allotropic form of nitrogen found in nature is molecular nitrogen (N
2) and why novel strategies of synthesizing polynitrogen allotropes in a cost-efficient manner are so highly sought after.

See also

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References

  1. ↑ Rutherford, Daniel (1772). De aere fixo dicto, aut mephitico [On air said to be fixed or mephitic]. University of Edinburgh: Balfour & Smellie.
  2. ↑ Curtius, Theodor (1890). "Ueber Stickstoffwasserstoffsäure (Azoimid) N3H" [On Hydrazoic Acid (Azoimide) N3H]. Berichte der Deutschen Chemischen Gesellschaft (in German). 23 (2): 3023–3033. doi:10.1002/cber.189002302232.
  3. ↑ Christe, Karl O.; Wilson, William W.; Sheehy, Jeffrey A.; Boatz, Jerry A. (12 Jul 1999). "N +
    5    : A Novel Homoleptic Polynitrogen Ion as a High Energy Density Material"    . Angewandte Chemie International Edition. 38 (13–14): 2004–2009. doi: 10.1002/(SICI)1521-3773(19990712)38:13/14<2004::AID-ANIE2004>3.0.CO;2-7 . PMID   34182671.
  4. ↑ Glukhovtsev, Mikhail N.; Jiao, Haijun; Schleyer, Paul von Ragué (January 1996). "Besides N2, What Is the Most Stable Molecule Composed Only of Nitrogen Atoms?". Inorganic Chemistry. 35 (24): 7124–7133. doi:10.1021/ic9606237. PMID   11666896.
  5. ↑ Junk, Gregor (1 June 1958). "The Presence of N +
    3     and N+
    4     in the Mass Spectra of Molecular Nitrogen". Journal of the American Chemical Society. 80 (11): 2908–2909. doi:10.1021/ja01544a085.
  6. ↑ Stephan, K.; Märk, T. D.; Futrell, J. H.; Helm, H. (1 April 1984). "Electron impact ionization of (N2)2: Appearance energies of N+
    3     and N+
    3    ". Journal of Chemical Physics. American Institute of Physics (published 31 August 1998) (80): 3185. doi:10.1063/1.44714.    {{cite journal}}: CS1 maint: multiple names: authors list (link), as cited in Tosi, P.; Lu, W. Y.; Bassi, D.; Tarroni, R. (1 February 2001). "The reaction N +
    2     + N
    2     → N+
    3     + N from thermal to 25 eV". Journal of Chemical Physics. 114 (5): 2149–2153. doi:10.1063/1.1336808.
  7. 1 2 3 4 5 6 Cacace, F.; de Petris, G.; Troiani, A. (18 January 2002). "Experimental Detection of Tetranitrogen". Science. 295 (5554): 480–481. Bibcode:2002Sci...295..480C. doi:10.1126/science.1067681. PMID   11799238. S2CID   35745247.
  8. 1 2 Nguyen, Minh Tho (September 2003). "Polynitrogen compounds: 1. Structure and stability of N4 and N5 systems". Coordination Chemistry Reviews. 244 (1–2): 93–113. doi:10.1016/S0010-8545(03)00101-2.
  9. 1 2 Zarko, V. E. (2010). "Searching for ways to create energetic materials based on polynitrogen compounds (review)". Combustion, Explosion, and Shock Waves. 46 (22): 121–131. doi:10.1007/s10573-010-0020-x. S2CID   95184003.
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