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Diphosphene

From Wikipedia, the free encyclopedia
For the functional group, seeDiphosphene (functional group).
Diphosphene
Ball and stick model of diphosphene molecule
Ball and stick model of diphosphene molecule
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/H2P2/c1-2/h1-2H checkY
    Key: SWJAOBXRZSMKNS-UHFFFAOYSA-N checkY
Properties
P
2
H
2
Molar mass63.96340 g·mol−1
Related compounds
Otheranions
diazene
Othercations
diphosphenes
Related Binaryazenes
triazene
tetrazene
Related compounds
ammonia
diazane
triazane
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Chemical compound

Diphosphene is a compound having the formula (PH)2. It exists as twogeometric isomers,E andZ.[1] Diphosphene is also the parent member of the entire class ofdiphosphene compounds with the formula (PR)2, where R is anorganyl group.[2]

Visible radiation induces cis-trans isomerization,[3] although further irradiation can excite the molecule to a tripletdiradical state. In triplet trans-HPPH, the P-P bond length is predicted to be 2.291 Å. It is not only longer than the P-P double bond in ground state trans-bis(2,4,6-tri-tert-butylphenyl)diphosphene, but also longer than that of P-P single bond in H2PPH2. Calculation of the dihedral angle of trans-HPPH suggests that it is almost 90 degree, which means the formation ofπ{\displaystyle \pi } andπ{\displaystyle \pi ^{*}} P-P bonds is forbidden and σ bond is enhanced.[4]

References

[edit]
  1. ^Lu, T.; Simmonett, A. C.; Evangelista, F. A.; Yamaguchi, Y.; Schaefer, H. F. (2009). "Diphosphene and Diphosphinylidene".The Journal of Physical Chemistry A.113 (47):13227–13236.Bibcode:2009JPCA..11313227L.doi:10.1021/jp904028a.PMID 19594123.
  2. ^Yoshifuji, M.; Shibayama, K.; Inamoto, N.; Hirotsu, K.; Higuchi, T. (1983). "Reaction of the diphosphene ArP=PAr (Ar = 2,4,6-But3C6H2) with sulphur: isolation and X-ray structure of the diphosphene monosulphide".Journal of the Chemical Society, Chemical Communications.1983 (16):862–863.doi:10.1039/C39830000862.
  3. ^Caminade, Anne-Marie; Verrier, Martine; Ades, Claude; Paillous, Nicole; Koenig, Max (1984-01-01). "Laser irradiation of a diphosphene: evidence for the first cis–trans isomerization".J. Chem. Soc., Chem. Commun. (13):875–877.doi:10.1039/c39840000875.ISSN 0022-4936.
  4. ^Lu, Tongxiang; Hao, Qiang; Simmonett, Andrew C.; Evangelista, Francesco A.; Yamaguchi, Yukio; Fang, De-Cai; Schaefer, Henry F. (2010-10-14). "Low-Lying Triplet States of Diphosphene and Diphosphinylidene".The Journal of Physical Chemistry A.114 (40):10850–10856.Bibcode:2010JPCA..11410850L.doi:10.1021/jp105281w.ISSN 1089-5639.PMID 20836526.
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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