Phosphorus pentaiodide

Phosphorus pentaiodide
Names
IUPAC name
Phosphorus(V) iodide
Other names
  • Pentaiodophosphorane
  • Pentaiodophosphorus
  • Phosphorus pentaiodide
  • Tetraiodophosphonium iodide
Identifiers
CompTox Dashboard (EPA)
  • DTXSID30504485 Edit this at Wikidata
Properties
Chemical formula
PI5
Molar mass 665.49611 g·mol−1
Appearance Brown-black crystalline solid (disputed)[1]
Melting point 41 °C (106 °F; 314 K) (disputed)[1]
Related compounds
Related compounds
  • Phosphorus pentafluoride
  • Phosphorus pentachloride
  • Phosphorus pentabromide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound

Phosphorus pentaiodide is a hypothetical inorganic compound with formula PI5. The existence of this compound has been claimed intermittently since the early 1900s.[2] The claim is disputed: "The pentaiodide does not exist (except perhaps as PI3·I2, but certainly not as [PI4]+I...)".[3]

Claims

Phosphorus pentaiodide was reported to be a brown-black crystalline solid melting at 41 °C produced by the reaction of lithium iodide and phosphorus pentachloride in methyl iodide, however, this claim is disputed and probably generated a mixture of phosphorus triiodide and iodine.[1][4]

Although phosphorus pentaiodide has been claimed to exist in the form of [PI4]+I (tetraiodophosphonium iodide), experimental and theoretical data refutes this claim.[5][1]

Derivatives

Unlike the elusive PI5, the [PI4]+ cation (tetraiodophosphonium cation) is widely known. This cation is known with the anions tetraiodoaluminate [AlI4], hexafluoroarsenate [AsF6], hexafluoroantimonate [SbF6] and tetraiodogallate [GaI4]. [4][5]

References

  1. ^ a b c d N. G. Feshchenko; V. G. Kostina; A. V. Kirsanov (1978). "Chem Inform Abstract: SYNTHESIS OF PHOSPHORUS PENTAIODIDE". Russian Journal of General Chemistry. 48 (23): 195. doi:10.1002/chin.197823039.
  2. ^ Walker and Johnson, J. Chem. Soc. 87, 1595 (1905).
  3. ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
  4. ^ a b Inis Tornieporth-Getting; Thomas Klapötke (1990). "The preparation and characterization by Raman spectroscopy of Pl4+AsF6– containing the tetraiodophosphonium cation". Journal of the Chemical Society, Chemical Communications (2): 132–133. doi:10.1039/C39900000132.
  5. ^ a b Martin Kaupp; Christoph Aubauer; Günter Engelhardt; Thomas M. Klapötke; Olga L. Malkina (1999). "The PI+4 cation has an extremely large negative 31P nuclear magnetic resonance chemical shift, due to spin–orbit coupling: A quantum-chemical prediction and its confirmation by solid-state nuclear magnetic resonance spectroscopy". The Journal of Chemical Physics. 110 (8): 3897–3902. Bibcode:1999JChPh.110.3897K. doi:10.1063/1.478243.
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Phosphides
Other compounds
  • PBr3
  • PBr5
  • PBr7
  • PCl3
  • PCl5
  • P2Cl4
  • PF3
  • PF5
  • PI3
  • PH3
  • PN
  • P3N5
  • PO
  • P2O3
  • P2O4
  • P2O5
  • P4S3
  • P4Sx
  • P4S10
  • v
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  • e
Salts and covalent derivatives of the iodide ion
HI
+H
He
LiI BeI2 BI3
+BO3
CI4
+C
NI3
NH4I
+N
I2O4
I2O5
I2O6
I4O9
IF
IF3
IF5
IF7
Ne
NaI MgI2 AlI
AlI3
SiI4 PI3
P2I4
+P
PI5
S2I2 ICl
ICl3
Ar
KI CaI2 ScI3 TiI2
TiI3
TiI4
VI2
VI3
CrI2
CrI3
CrI4
MnI2 FeI2
FeI3
CoI2 NiI2
-Ni
CuI ZnI2 GaI
GaI3
GeI2
GeI4
+Ge
AsI3
As2I4
+As
Se IBr
IBr3
Kr
RbI
RbI3
SrI2 YI3 ZrI2
ZrI3
ZrI4
NbI4
NbI5
MoI2
MoI3
TcI3 RuI3 RhI3 PdI2 AgI CdI2 InI
InI3
SnI2
SnI4
SbI3
+Sb
TeI4
+Te
I
I
3
Xe
CsI
CsI3
BaI2   LuI3 HfI3
HfI4
TaI4
TaI5
WI2
WI3
WI4
ReI3
ReI
4
OsI
OsI2
OsI3
IrI3
IrI
4
PtI2
PtI4
AuI
AuI3
Hg2I2
HgI2
TlI
TlI3
PbI2 BiI3 PoI2
PoI4
AtI Rn
Fr RaI2   Lr Rf Db Sg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
LaI2
LaI3
CeI2
CeI3
PrI2
PrI3
NdI2
NdI3
PmI3 SmI2
SmI3
EuI2
EuI3
GdI2
GdI3
TbI3 DyI2
DyI
3
HoI3 ErI3 TmI2
TmI3
YbI2
YbI3
AcI3 ThI2
ThI3
ThI4
PaI4
PaI5
UI3
UI4
NpI3 PuI3 AmI2
AmI3
CmI3 BkI
3
CfI
2

CfI
3
EsI2
EsI3
Fm Md No
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