phosphine oxide
{{Short description|Chemical compound}}
{{See also|Phosphine oxides}}
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|Section1={{Chembox Identifiers
| CASNo = 13840-40-9
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| PubChem = 57448882
| StdInChI=1S/H3OP/c1-2/h2H3
| StdInChIKey = MPQXHAGKBWFSNV-UHFFFAOYSA-N
| SMILES = [O-][PH3+]
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|Section2={{Chembox Properties
| P = 1|H = 3|O= 1
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Phosphine oxide is the inorganic compound with the formula H3PO. Although stable as a dilute gas, liquid or solid samples are unstable. Unlike many other compounds of the type POxHy, H3PO is rarely discussed and is not even mentioned in major sources on main group chemistry.{{Greenwood&Earnshaw2nd|page 510}}
H3PO has been detected by mass spectrometry as a reaction product of oxygen and phosphine,{{cite journal | last1 = Hamilton | first1 = Peter A. | last2 = Murrells | first2 = Timothy P. | year = 1985 | title = Kinetics and mechanism of the reactions of PH3 with O(3P) and N(4S) atoms| journal = J. Chem. Soc., Faraday Trans. | volume = 2 | issue = 81| pages = 1531–1541 | doi = 10.1039/F29858101531}} by means of FT-IR in a phosphine-ozone reaction{{cite journal | last1 = Withnall | first1 = Robert | last2 = Andrews | first2 = Lester | year = 1987 | title = FTIR spectra of the photolysis products of the phosphine-ozone complex in solid argon| journal = J. Phys. Chem. | volume = 91 | issue = 4| pages = 784–797 | doi = 10.1021/j100288a008}}
Generation
Phosphine oxide has been claimed as the product of a reaction of phosphine with vanadium oxytrichloride as well as with chromyl chloride. The product was obtained by matrix isolation.{{cite journal | last1 = Kayser | first1 = David A. | last2 = Ault | first2 = Bruce S. | year = 2003 | title = Matrix Isolation and Theoretical Study of the Photochemical Reaction of PH3 with OVCl3 and CrCl2O2| journal = J. Phys. Chem. A | volume = 107 | issue = 33| pages = 6500–6505 | doi = 10.1021/jp022692e | bibcode = 2003JPCA..107.6500K}} It has also been reported relatively stable in a water-ethanol solution by electrochemical oxidation of white phosphorus, where it slowly disproportionates into phosphine and hypophosphorous acid.{{cite journal | last1 = Yakhvarov | first1 = D. | last2 = Caporali | first2 = M. | last3 = Gonsalvi | first3 = L. | last4 = Latypov | first4 = S. | last5 = Mirabello | first5 = V. | last6 = Rizvanov | first6 = I. | last7 = Sinyashin | first7 = O. | last8 = Stoppioni | first8 = P. | last9 = Peruzzini | first9 = M. | year = 2011 | title = Experimental Evidence of Phosphine Oxide Generation in Solution and Trapping by Ruthenium Complexes | journal = Angewandte Chemie International Edition | volume = 50 | issue = 23 | pages = 5370–5373 | doi = 10.1002/anie.201100822 | pmid=21538749}}
Phosphine oxide is reported as an intermediate in the room-temperature polymerization of phosphine and nitric oxide to solid PxHy.{{cite journal | last1 = Zhao | first1 = Yi-Lei | last2 = Flora | first2 = Jason W. | last3 = David Thweatt | first3 = William | last4 = Garrison | first4 = Stephen L. | last5 = Gonzalez | first5 = Carlos | last6 = Houk | first6 = K. N. | last7 = Marquez | first7 = Manuel | year = 2009 | title = Phosphine Polymerization by Nitric Oxide: Experimental Characterization and Theoretical Predictions of Mechanism|journal = Inorg. Chem. | volume = 48 | issue = 3| pages = 1223–1231 | doi = 10.1021/ic801917a| pmid = 19102679 }}
Further reading
- {{cite journal |doi=10.1021/ja984314m |title=The Electron Localization Function (ELF) Description of the PO Bond in Phosphine Oxide |date=1999 |last1=Chesnut |first1=D. B. |last2=Savin |first2=A. |journal=Journal of the American Chemical Society |volume=121 |issue=10 |pages=2335–2336 }}
- {{cite journal |doi=10.1021/jp411623h |title=Pnicogen Bonds between X═PH3 (X = O, S, NH, CH2) and Phosphorus and Nitrogen Bases |date=2014 |last1=Alkorta |first1=Ibon |last2=Sánchez-Sanz |first2=Goar |last3=Elguero |first3=José |last4=Del Bene |first4=Janet E. |journal=The Journal of Physical Chemistry A |volume=118 |issue=8 |pages=1527–1537 | pmid=24547683 |bibcode=2014JPCA..118.1527A }}
References
{{Reflist|30em}}