Organoxenon compound

Organoxenon compounds in organic chemistry contain carbon to xenon chemical bonds. The first organoxenon compounds were divalent, such as (C6F5)2Xe. The first tetravalent organoxenon compound, [C6F5XeF2][BF4], was synthesized in 2004.[1] So far, more than one hundred organoxenon compounds have been researched.

Most of the organoxenon compounds are more unstable than xenon fluorides due to the high polarity. The molecular dipoles of xenon difluoride and xenon tetrafluoride are both 0 D. The early synthesized ones only contain perfluoro groups, but later some other groups were found, e.g. 2,4,6-trifluorophenyl.[2]

Xe(II)

The most common bivalent organoxenon compound is C6F5XeF, which is always used as a precursor to other organoxenon compounds. Due to the instability of xenon fluoride, it is impossible to synthesize organoxenon compounds by using general organic reagents. Most frequently used fluorinating agents include Cd(ArF)2(subscript "F" means fluorine-including aryl), C6F5SiF3, and C6F5SiMe3 (should be used along with fluoride).

With the use of stronger Lewis acids, such as C6F5BF2, ionic compounds like [RXe][ArFBF3] can be produced. Alkenyl and alkyl organoxenon compounds are prepared in this way as well, for example, C6F5XeCF=CF2 and C6F5XeCF3.[2]

Some typical reactions are listed below:

The third reaction also produces (C6F5)2Xe, Xe(2,4,6-C6H2F3)2 and so on.

The precursor C6F5XeF can be prepared by the reaction of trimethyl(pentaflurophenyl)silane (C6F5SiMe3) and xenon difluoride. Adding fluoride to the adduct of C6F5XeF and arsenic pentafluoride is another method.[2]

Arylxenon compounds with fewer fluorine substituents are also known. For instance, 2,6-F2C6H3Xe+BF4− and 4-FC6H4Xe+BF4− have been prepared, and a crystal structure of the former has been obtained, consisting of a formally 1-coordinate Xe with a long, weak contact with a F on the tetrafluoroborate anion.[3][4]

Xe(IV)

In 2000, Karel Lutar and Boris Žemva et al. produced an ionic compound. They treated xenon tetrafluoride and difluoro(pentaflurophenyl)borane in dichloromethane at -55 °C:

The compound is an extremely strong fluorinating agent, and it is capable of converting (C6F5)3P to (C6F5)3PF2, C6F5I to C6F5IF2, and iodine to iodine pentafluoride.[1]

See also

  • Compounds of carbon with other elements in the periodic table:
Compounds of carbon with other elements in the periodic table
CH He
CLi CBe CB CC CN CO CF Ne
CNa CMg CAl CSi CP CS CCl CAr
CK CCa CSc CTi CV CCr CMn CFe CCo CNi CCu CZn CGa CGe CAs CSe CBr CKr
CRb CSr CY CZr CNb CMo CTc CRu CRh CPd CAg CCd CIn CSn CSb CTe CI CXe
CCs CBa CHf CTa CW CRe COs CIr CPt CAu CHg CTl CPb CBi CPo CAt Rn
Fr CRa Rf Db CSg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
↓
CLa CCe CPr CNd CPm CSm CEu CGd CTb CDy CHo CEr CTm CYb CLu
Ac CTh CPa CU CNp CPu CAm CCm CBk CCf CEs Fm Md No Lr
Chemical bonds to carbon
Core organic chemistry Many uses in chemistry
Academic research, but no widespread use Bond unknown

References

  1. 1 2 LeBlond, Nicolas, Lutar, Karel, Žemva, Boris (2000-01-16). "The First Organoxenon(IV) Compound: Pentafluorophenyldifluoroxenonium(IV) Tetrafluoroborate". Angewandte Chemie International Edition. 39 (2): 391–393. doi:10.1002/(SICI)1521-3773(20000117)39:2<391::AID-ANIE391>3.0.CO;2-U.
  2. 1 2 3 FROHN, H (2004-05-31). "C6F5XeF, a versatile starting material in xenon-carbon chemistry". Journal of Fluorine Chemistry. 125 (6): 981–988. doi:10.1016/j.jfluchem.2004.01.019.
  3. ↑ Gilles, T.; Gnann, R.; Naumann, D.; Tebbe, K. F. (1994-03-15). "2,6-Difluorphenylxenon(II)-tetrafluoroborat". Acta Crystallographica Section C. 50 (3): 411–413. doi:10.1107/s0108270193009898. ISSN 0108-2701.
  4. ↑ Naumann, D.; Butler, H.; Gnann, R.; Tyrra, W. (1993-03-01). "Arylxenon tetrafluoroborates: compounds of unexpected stability". Inorganic Chemistry. 32 (6): 861–863. doi:10.1021/ic00058a018. ISSN 0020-1669.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.