Dioxygenyl

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Dioxygenyl-ion-2D-dimensions.png

The dioxygenyl ion, O2+, is a rarely encountered oxycation in which both oxygen atoms have a formal oxidation state of +½. It is formally derived from oxygen by the removal of an electron:

O2 → O2+ + e

The energy change for this process is called the ionization energy of the oxygen molecule. Relative to most molecules, this ionization energy is very high at 1175 kJ/mol.[1] As a result, the scope of the chemistry of O2+ is quite limited, acting mainly as a 1-electron oxidiser.[2]

Structure and molecular properties[edit]

O2+ has a bond order of 2.5, and a bond length of 112.3 pm in solid O2[AsF6].[3] It has the same number of valence electrons as nitric oxide. The bond energy is 625.1 kJ mol−1 and the stretching frequency is 1858 cm−1,[4] both of which are high relative to most molecules.

Synthesis[edit]

The reaction of oxygen, O2, with platinum hexafluoride, PtF6, yields dioxygenyl hexafluoroplatinate, O2+[PtF6]-:

O2 + PtF6 → O2+[PtF6]

PtF6 is one of the few oxidising agents sufficiently powerful to oxidise O2.

Dioxygenyl hexafluoroplatinate played a pivotal role in the discovery of noble gas compounds. After Neil Bartlett found that PtF6 could oxidise O2 to O2+, he investigated its reaction with noble gases and discovered xenon hexafluoroplatinate.

O2+ is also found in similar compounds of the form O2MF6, where M is arsenic (As),[5] gold (Au),[6] niobium (Nb), ruthenium (Ru), rhenium (Re), rhodium (Rh),[7] vanadium (V),[8] or phosphorus (P).[9] Other forms are also attested, including O2GeF5 and (O2)2SnF6.[8]

The tetrafluoroborate and hexafluorophosphate salts may be prepared by the reaction of dioxygen difluoride with boron trifluoride or phosphorus pentafluoride at −126 °C:[9]

2 O2F2 + 2 BF3 → 2 O2BF4 + F2
2 O2F2 + 2 PF5 → 2 O2PF6 + F2

These compounds rapidly decompose at room temperature:

2 O2BF4 → 2 O2 + F2 + 2 BF3
2 O2PF6 → 2 O2 + F2 + 2 PF5

Reactions[edit]

The reaction of O2BF4 with xenon at 173 K produces a white solid believed to be F–Xe–BF2, containing an unusual xenon-boron bond:[10]

2 O2BF4 + 2 Xe → 2 O2 + F2 + 2 FXeBF2

The dioxygenyl salts O2BF4 and O2AsF6 react with carbon monoxide to give oxalyl fluoride, F–(C=O)–(C=O)–F, in high yield.[11]

References[edit]

  1. ^ Michael Clugston; Rosalind Flemming (2000). Advanced Chemistry, Oxford University Press, ISBN 0-19-914633-0, ISBN 978-0-19-914633-8, p. 355.
  2. ^ Foote, Christopher S.; Valentine, Joan S. (1995). Active oxygen in chemistry. Joel F. Liebman, A. Greenberg. Springer. ISBN 0-412-03441-7. 
  3. ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 0080379419.  p. 616
  4. ^ J. Shamir, J. Binenboym, H. H. Claassen (1968). "The vibrational frequency of the O2+ cation". J. Am. Chem. Soc. 90 (22): 6223−6224. doi:10.1021/ja01024a054. 
  5. ^ A. R. Young, T. Hirata, S. I. Morrow (1964). "The Preparation of Dioxygenyl Salts from Dioxygen Difluoride". J. Am. Chem. Soc. 86 (1): 20−22. doi:10.1021/ja01055a006. 
  6. ^ Nakajima, Tsuyoshi (1995). Fluorine-carbon and fluoride-carbon materials: chemistry, physics, and applications. CRC Press. ISBN 0-8247-9286-6. 
  7. ^ Vasile, M. J.; Falconer, W. E. (1975). "Vapour transport of dioxygenyl salts". Journal of the Chemical Society Dalton Transactions (4): 316–318. doi:10.1039/DT9750000316.  edit
  8. ^ a b Holleman, Arnold F.; Wiberg, Egon (2001). Inorganic chemistry. Academic Press. p. 475. ISBN 0-12-352651-5. 
  9. ^ a b Solomon, I. J.; Brabets, R. I.; Uenishi, R. K.; Keith, J. N.; McDonough, J. M. (1964). "New Dioxygenyl Compounds". Inorganic Chemistry 3 (3): 457. doi:10.1021/ic50013a036.  edit
  10. ^ Goetschel, C. T.; Loos, K. R. (1972). "Reaction of xenon with dioxygenyl tetrafluoroborate. Preparation of FXe-BF2". Journal of the American Chemical Society 94 (9): 3018–3021. doi:10.1021/ja00764a022.  edit
  11. ^ Pernice, H.; Willner, H.; Eujen, R. (2001). "The reaction of dioxygenyl salts with 13
    CO Formation of F13
    C(O)13
    C(O)F". Journal of Fluorine Chemistry 112 (2): 277–590. doi:10.1016/S0022-1139(01)00512-7.
      edit