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Fluorine azide

From Wikipedia, the free encyclopedia
Fluorine azide
Names
Other names
triazadienyl fluoride
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/FN3/c1-3-4-2
    Key: AJXWEJAGUZJGRI-UHFFFAOYSA-N
  • [N-]=[N+]=NF
Properties
FN3
Molar mass61.019 g/mol
AppearanceYellow-green gas
Density1.3 g/cm3[1]
Melting point−139 °C (−218 °F; 134 K)[2]
Boiling point−30 °C (−22 °F; 243 K)[2]
Explosive data
Shock sensitivityExtreme
Friction sensitivityExtreme
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Extremely sensitive explosive
NFPA 704 (fire diamond)
Related compounds
Othercations
Hydrazoic acid
Chlorine azide
Bromine azide
Iodine azide
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Fluorine azide ortriazadienyl fluoride is a yellow green gas composed ofnitrogen andfluorine with formulaFN3.[3] Its properties resemble those ofClN3,BrN3, andIN3.[4] The bond between the fluorine atom and the nitrogen is very weak, leading to this substance being very unstable and prone to explosion.[5] Calculations show the F–N–N angle to be around 102° with a straight line of 3 nitrogen atoms.[6]

It was first made by John F. Haller in 1942.[7]

Reactions

[edit]

Fluorine azide can be made by reactinghydrazoic acid orsodium azide, with fluorine gas.[2][8]

HN3 + F2 → N3F + HF
NaN3 + F2 → N3F + NaF

Fluorine azide decomposes without explosion at normal temperatures to makedinitrogen difluoride:

2 FN3 → N2F2 + 2 N2.[3]

At higher temperatures such as 1000 °C fluorine azide breaks up intonitrogen monofluoride radical:[8]

FN3 → NF + N2

The FN itself dimerizes on cooling.

2 NF → N2F2

Solid or liquidFN3 can explode, releasing a large amount of energy. A thin film burns at the rate of 1.6 km/s.[9] Due to the explosion hazard, only very small quantities of this substance should be handled at a time.[10]

FN3adducts can be formed with theLewis acidsboron trifluoride (BF3) andarsenic pentafluoride (AsF5) at -196 °C. These molecules bond with the first nitrogen atom from the fluorine.[11]

Properties

[edit]

Spectroscopy

[edit]
ParameterValue[10]Unit
A48131.448MHz
B5713.266MHz
C5095.276MHz
μa1.1
μb0.7

Shape

[edit]

Distances between atoms are F–N 0.1444 nm, FN=NN 0.1253 nm and FNN=N 0.1132 nm.[10]

Physical

[edit]

FN3adsorbs on to solid surfaces ofpotassium fluoride, but not ontolithium fluoride orsodium fluoride. This property was being investigated so thatFN3 could boost the energy of solid propellants.[1]

The ultravioletphotoelectric spectrum shows ionisation peaks at 11.01, 13,72, 15.6, 15.9, 16.67, 18.2, and 19.7 eV. Respectively these are assigned to the orbitals: π, nN or nF, nF, πF, nN or σ, π and σ.[5]

References

[edit]
  1. ^abBrener, Nathan E.; Kestner, Neil R.; Callaway, Joseph (December 1990).Theoretical Studies of Highly Energetic CBES Materials: Final Report for the Period 2 March 1987 to 31 May 1987(PDF). Louisiana State University, Department of Physics and Astronomy. pp. 21–27.Archived(PDF) from the original on March 3, 2016. Retrieved25 June 2014.
  2. ^abcGholivand, Khodayar; Gabriele Schatte; Helge Willner (1987). "Properties of triazadienyl fluoride, N3F".Inorganic Chemistry.26 (13):2137–2140.doi:10.1021/ic00260a025.ISSN 0020-1669.
  3. ^abGipstein, Edward; John F. Haller (1966). "Absorption Spectrum of Fluorine Azide".Applied Spectroscopy.20 (6):417–418.Bibcode:1966ApSpe..20..417G.doi:10.1366/000370266774386470.ISSN 0003-7028.S2CID 96337253.
  4. ^Saxena, P. B. (2007-01-01).Chemistry of Interhalogen Compounds. Discovery Publishing House. p. 96.ISBN 9788183562430. Retrieved16 June 2014.
  5. ^abRademacher, Paul; Andreas J. Bittner; Gabriele Schatte; Helge Willner (1988). "Photoelectron Spectrum and Electronic Structure of Triazadienyl Fluoride, N3F".Chemische Berichte.121 (3):555–557.doi:10.1002/cber.19881210325.ISSN 0009-2940.
  6. ^Peters, Nancy J. S.;Leland C. Allen; Raymond A. Firestone (1988). "Fluorine azide and fluorine nitrate: structure and bonding".Inorganic Chemistry.27 (4):755–758.doi:10.1021/ic00277a035.ISSN 0020-1669.
  7. ^Lowe, Derek (21 October 2008)."Things I Won't Work With: Triazadienyl Fluoride".In the Pipeline. Retrieved15 June 2014.
  8. ^abBenard, D. J.; B. K. Winker; T. A. Seder; R. H. Cohn (1989). "Production of nitrogen monofluoride (a1Δ) by dissociation of fluorine azide".The Journal of Physical Chemistry.93 (12):4790–4796.doi:10.1021/j100349a022.ISSN 0022-3654.
  9. ^Seder, T.A.; D.J. Benard (1991). "The decomposition of condensed phase fluorine azide".Combustion and Flame.85 (3–4):353–362.Bibcode:1991CoFl...85..353S.doi:10.1016/0010-2180(91)90139-3.ISSN 0010-2180.
  10. ^abcChristen, Dines.; H. G. Mack; G. Schatte; H. Willner (1988). "Structure of triazadienyl fluoride, FN3, by microwave, infrared, and ab initio methods".Journal of the American Chemical Society.110 (3):707–712.Bibcode:1988JAChS.110..707C.doi:10.1021/ja00211a007.ISSN 0002-7863.
  11. ^Schatte, G.; H. Willner (1991)."Die Wechselwirkung von N3F mit Lewis-Säuren und HF. N3F als möglicher Vorläufer für die Synthese von N3+-Salzen = The interaction of N3F with Lewis acids and HF•N3F as possible precursor for the synthesis of N3+ salts".Zeitschrift für Naturforschung B (in German).46 (4):483–489.doi:10.1515/znb-1991-0410.ISSN 0932-0776.S2CID 97045269.

External links

[edit]
Salts and covalent derivatives of thefluoride ion
HF?HeF2
LiFBeF2BF
BF3
B2F4
+BO3
CF4
CxFy
+CO3
NF3
FN3
N2F2
NF
N2F4
NF2
?NF5
+N
+NO3
OF2
O2F2
OF
O3F2
O4F2
?OF4
F2Ne
NaFMgF2AlF
AlF3
SiF4P2F4
PF3
PF5
+PO4
S2F2
SF2
S2F4
SF3
SF4
S2F10
SF6
+SO4
ClF
ClF3
ClF5
?ArF2
?ArF4
KFCaF
CaF2
ScF3TiF2
TiF3
TiF4
VF2
VF3
VF4
VF5
CrF2
CrF3
CrF4
CrF5
?CrF6
MnF2
MnF3
MnF4
?MnF5
FeF2
FeF3
FeF4
CoF2
CoF3
CoF4
NiF2
NiF3
NiF4
CuF
CuF2
?CuF3
ZnF2GaF2
GaF3
GeF2
GeF4
AsF3
AsF5
Se2F2
SeF4
SeF6
+SeO3
BrF
BrF3
BrF5
KrF2
?KrF4
?KrF6
RbFSrF
SrF2
YF3ZrF2
ZrF3
ZrF4
NbF4
NbF5
MoF4
MoF5
MoF6
TcF4
TcF
5

TcF6
RuF3
RuF
4

RuF5
RuF6
RhF3
RhF4
RhF5
RhF6
PdF2
Pd[PdF6]
PdF4
?PdF6
Ag2F
AgF
AgF2
AgF3
CdF2InF
InF3
SnF2
SnF4
SbF3
SbF5
TeF4
?Te2F10
TeF6
+TeO3
IF
IF3
IF5
IF7
+IO3
XeF2
XeF4
XeF6
?XeF8
CsFBaF2 LuF3HfF4TaF5WF4
WF5
WF6
ReF4
ReF5
ReF6
ReF7
OsF4
OsF5
OsF6
?OsF
7

?OsF
8
IrF2
IrF3
IrF4
IrF5
IrF6
PtF2
Pt[PtF6]
PtF4
PtF5
PtF6
AuF
AuF3
Au2F10
?AuF6
AuF5•F2
Hg2F2
HgF2
?HgF4
TlF
TlF3
PbF2
PbF4
BiF3
BiF5
PoF2
PoF4
PoF6
AtF
?AtF3
?AtF5
RnF2
?RnF
4

?RnF
6
FrFRaF2 LrF3RfDbSgBhHsMtDsRgCnNhFlMcLvTsOg
LaF3CeF3
CeF4
PrF3
PrF4
NdF2
NdF3
NdF4
PmF3SmF
SmF2
SmF3
EuF2
EuF3
GdF3TbF3
TbF4
DyF2
DyF3
DyF4
HoF3ErF3TmF2
TmF3
YbF2
YbF3
AcF3ThF2
ThF3
ThF4
PaF4
PaF5
UF3
UF4
UF5
UF6
NpF3
NpF4
NpF5
NpF6
PuF3
PuF4
PuF5
PuF6
AmF2
AmF3
AmF4
?AmF6
CmF3
CmF4
 ?CmF6
BkF3
BkF
4
CfF3
CfF4
EsF3
EsF4
?EsF6
FmMdF3No
PF6,AsF6,SbF6 compounds
AlF2−5,AlF3−6 compounds
chlorides, bromides, iodides
and pseudohalogenides
SiF2−6,GeF2−6 compounds
Oxyfluorides
Organofluorides
with transition metal,
lanthanide, actinide, ammonium
nitric acids
bifluorides
thionyl, phosphoryl,
and iodosyl
Nitrogen species
Hydrides
Organic
Oxides
Halides
Oxidation states
−3,−2,−1, 0,+1,+2,+3,+4,+5 (a stronglyacidic oxide)
Salts and covalent derivatives of theazide ion
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