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Nitrogen pentahydride

From Wikipedia, the free encyclopedia
Nitrogen pentahydride
A possible structure of nitrogen pentahydride according to theory calculations[1]
Names
Other names
Ammonium hydride
Identifiers
3D model (JSmol)
  • InChI=1S/H5N/h1H5
    Key: QPGNFWUGXLWWDO-UHFFFAOYSA-N
  • covalent: [NH5]
  • ionic: [H-].[NH4+]
Properties
H5N
Molar mass19.047 g·mol−1
Structure
Trigonal bipyramidal molecular geometry (covalent[1])
0D (covalent[1])
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Nitrogen pentahydride, also known asammonium hydride is ahypothetical compound with the chemical formula NH5. There are two theoretical structures of nitrogen pentahydride. One structure istrigonal bipyramidal molecular geometry type NH5 molecule. Itsnitrogen atom andhydrogen atoms arecovalently bounded, and itssymmetry group isD3h.[1] Another predicted structure of nitrogen pentahydride is anionic compound, composed of anammonium ion and ahydride ion (NH4+H). Until now, no one has synthesized this substance, or proved its existence, and related experiments have not directly observed nitrogen pentahydride. It is only speculated that it may be areactive intermediate based on reaction products. Theoretical calculations show this molecule is thermodynamically unstable.[4] The reason might be similar to the instability ofnitrogen pentafluoride,[5] so the possibility of its existence is low. However, nitrogen pentahydride might exist in special conditions or high pressure. Nitrogen pentahydride was considered for use as asolid rocket fuel for research in 1966.[6]

Research and attempts

[edit]

Some studies believe that nitrogen pentahydride may exist in the formation of other metal atomscrystal lattice, such asmercury[7][8] andlithium. There are also related studies to explore the possibility of a substitution reaction with ammonium halide.[9] There are also attempts to react ammonium anddeuterium to produce the pentahydride, however some experiments show that it may only be a reactive intermediate, which will immediately decompose into ammonia and hydrogen,[10][1] and the same is true for experiments using deuterium.[2][1] However, all the studies above are only theoretical calculations, the existence of nitrogen pentahydride has not been observed, and this substance has not been shown to exist.

An experimental attempted to do adisplacement reaction between ammonium trifluoroacetate andlithium hydride in the molten state, in order to study the possibility of the existence of nitrogen pentahydride:[10]

CF3COONH4 + LiH → CF3COOLi + [NH4H]

In the reaction between ammonium trifluoroacetate and lithium deuteride, the product ammonia contains 85% of ordinary ammonia and 15% of monodeuterated ammonia. The product hydrogen contains 66% ofhydrogen deuteride, 21% of hydrogen gas and 13% of deuterium gas. In the product collected using tetradeuterated ammonium trifluoroacetate and lithium hydride, ammonia contains ND3, NHD2 and NH2D, while hydrogen contains 68% of hydrogen deuteride, 18% of hydrogen gas and 14% of deuterium gas. Therefore, it is speculated that the reaction may have two routes: one is to directly decompose into ammonia and hydrogen, the other is to first generate ammonium deuteride reactive intermediates, partly by forming deuterium anions and hydrogen cations to form deuterated hydrogen and ammonia and by the formation of hydride ions or deuterium cations to decompose into hydrogen or deuterium gas.[1]

But it immediately decomposed into hydrogen and ammonia, and it was impossible to prove its existence. Experiments with deuterium still get the same results:[2]

[NH4H] → NH3 + H2

Structure

[edit]
Possible structures of covalently bounded nitrogen pentahydride[1]

Several papers have conducted theoretical calculations on nitrogen pentahydride, and believe that nitrogen pentahydride is unlikely to form ionic crystals of hydride and ammonium ions. However, it is possible that hydrogen is connected to one of the hydrogen atoms of ammonium.[1] It may also be similar tonitrogen pentafluoride, forming athree-center two-electron bond similar tocarbonium ions, or those five hydrogen atoms are arranged in a triangular bipyramid structure around the nitrogen atom.[1]

Related compounds

[edit]

A compound that is similar to nitrogen pentahydride is the theoreticalnitrogen pentafluoride. Its structure is assumed to be tetrafluoroammonium fluoride (NF4+F).[11] Similarly to nitrogen pentahydride, it is a compound of nitrogen and five of the same atom, but nitrogen pentafluoride is also a hypothetical compound, still never synthesized and only theoretical research exist.[12] Other pnictogen pentahydrides are theoretically more stable, such asphosphorus pentahydride (PH4H) which is more stable than nitrogen pentahydride but still unstable to decomposition tophosphine and hydrogen gas. Its organic derivatives (phosphoranes) are more stable, such as stablepentaphenylphosphorus (Ph5P).[13] Other heavier pnictogen pentahydrides are more likely to exist, such as the theoreticalarsenic pentahydride.[14][better source needed]

References

[edit]
  1. ^abcdefghijOlah, G.A.; Prakash, G.K.S. (2003).Across Conventional Lines: Selected Papers of George A Olah(In 2 Volumes). World Scientific Series in 20th Century Chemistry. p. 759.ISBN 978-981-4498-54-8. Archived fromthe original on November 25, 2021.
  2. ^abcMerlet, P. and Koschel, D. and Hack, W. and Haubold, R. and Ohms-Bredemann, U. and Heinrich-Sterzel, C. and Wagner, J. and Keller-Rudek, H. and Schi{\"o}berg, D. and Strametz, C. (2013).N Nitrogen: Compounds with Noble Gases and Hydrogen. Gmelin Handbook of Inorganic and Organometallic Chemistry - 8th edition. Springer Berlin Heidelberg. p. 278.ISBN 978-3-662-06333-0.Archived from the original on 2017-08-16.{{cite book}}: CS1 maint: multiple names: authors list (link)
  3. ^Hisham, Mohamed W. M. and Benson, Sidney W. (1988). "Thermochemistry of inorganic solids. 8. Empirical relations among the enthalpies of formation of different anionic compounds".The Journal of Physical Chemistry.92 (21):6107–6112.doi:10.1021/j100332a052.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  4. ^Ewig, Carl S.; Van Wazer, John R. (1989). "Ab initio studies of molecular structures and energetics. 3. Pentacoordinated nitrogen NFnH5-n compounds".Journal of the American Chemical Society.111 (12):4172–4178.doi:10.1021/ja00194a005.
  5. ^Kurzydłowski, Dominik; Zaleski-Ejgierd, Patryk (December 2016)."Hexacoordinated nitrogen(V) stabilized by high pressure".Scientific Reports.6 (1) 36049.Bibcode:2016NatSR...636049K.doi:10.1038/srep36049.PMC 5093683.PMID 27808104.
  6. ^Sterrett, K. F.; Caron, A. P. (1966)."High pressure chemistry of hydrogenous fuels". Northrop Space Labs. Archived fromthe original on 2011-08-23. Retrieved2017-08-21.
  7. ^Bard, A.J. and Inzelt, G. and Scholz, F. (2012).Electrochemical Dictionary. Springer Berlin Heidelberg.ISBN 978-3-642-29550-8.LCCN 2012945766.Archived from the original on 2017-08-16.{{cite book}}: CS1 maint: multiple names: authors list (link)
  8. ^Gladyshev, VP; Kovaleva, SV; Khramtsova, NA (2001). "Determination of ammonium by stripping voltammetry".Journal of Analytical Chemistry.56 (5). Springer:443–448.doi:10.1023/A:1016627003444.S2CID 195095419.
  9. ^Olah, George A.; Donovan, Daniel J.; Shen, Jacob; Klopman, Gilles (1975). "Onium ions. XVI. Hydrogen-deuterium exchange accompanying the cleavage of ammonium (tetradeuterioammonium) trifluoroacetate by lithium deuteride (hydride) indicating SN2 like nucleophilic displacement at quaternary nitrogen through pentacoordinated ammonium hydride".Journal of the American Chemical Society.97 (12):3559–3561.doi:10.1021/ja00845a069.
  10. ^abOlah, G. A,; Donovan, D. J.;Shen, J.; Klopman, G.(J. Am. Chem. Soc. 97 [1975] 3559/61).
  11. ^Goetschel, C. T.; V. A. Campanile; R. M. Curtis; K. R. Loos; C. D. Wagner; J. N. Wilson (July 1972). "Preparation and properties of perfluoroammonium tetrafluoroborate, NF4+BF4-, and possible synthesis of nitrogen pentafluoride".Inorganic Chemistry.11 (7):1696–1701.doi:10.1021/ic50113a051.
  12. ^Lewars, Errol G. (2008-11-03).Modeling marvels: computational anticipation of novel molecules. Springer. pp. 53–67.ISBN 978-1-4020-6973-4.Archived from the original on 2015-02-12.
  13. ^^A Guide to Organophosphorus Chemistry Louis D. Quin2000 John Wiley & Sons ISBN 0-471-31824-8
  14. ^"arsorane".CHEBI.Archived from the original on 2017-08-21. Retrieved2017-08-21.
Nitrogen species
Hydrides
Organic
Oxides
Halides
Oxidation states
−3,−2,−1, 0,+1,+2,+3,+4,+5 (a stronglyacidic oxide)
Alkali metal
(Group 1) hydrides
Alkaline (Group 2)
earth hydrides
Monohydrides
Dihydrides
Group 13
hydrides
Boranes
Alanes
Gallanes
Indiganes
Thallanes
Nihonanes(predicted)
  • NhH
  • NhH3
  • Nh2H6
  • NhH5
Group 14 hydrides
Hydrocarbons
Silanes
Silenes
Silynes
Germanes
Stannanes
Plumbanes
Flerovanes(predicted)
  • FlH
  • FlH2
  • FlH4
Pnictogen
(Group 15) hydrides
Azanes
Azenes
Phosphanes
Phosphenes
Arsanes
Stibanes
Bismuthanes
Moscovanes
Hydrogen
chalcogenides
(Group 16 hydrides)
Polyoxidanes
Polysulfanes
Selanes
Tellanes
Polanes
Livermoranes
Hydrogen halides
(Group 17 hydrides)
  • HF
  • HCl
  • HBr
  • HI
  • HAt
  • HTs(predicted)
  • Transition
    metal hydrides
    Lanthanide
    hydrides
    Actinide
    hydrides
    Exotic matter hydrides
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