Bis(pentafluorophenyl)xenon

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Bis(pentafluorophenyl)xenon
Bis(pentafluorophenyl)xenon conformation.png
Names
IUPAC name
bis(2,3,4,5,6-pentafluorophenyl)xenon
Identifiers
  • 328379-54-0
3D model (JSmol)
ChemSpider
  • InChI=1S/C12F10Xe/c13-1-3(15)7(19)11(8(20)4(1)16)23-12-9(21)5(17)2(14)6(18)10(12)22
    Key: YAQWCIUPEXZIQW-UHFFFAOYSA-N
  • C1(=C(C(=C(C(=C1F)F)[Xe]C2=C(C(=C(C(=C2F)F)F)F)F)F)F)F
Properties
C12F10Xe
Molar mass 465.409 g·mol−1
Density 2.447 g/cm3 (at 50 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Bis(pentafluorophenyl)xenon is an unstable organic compound of xenon. It consists of two fluoronated phenyl rings connected to xenon.

Structure[]

Bis(pentafluorophenyl)xenon is a molecular substance. In the solid form it crystallises in the monoclinic system with space group P21/n.[1] The unit cell has four molecules with a=13.635 Å b=8.248 Å c=11.511 Å, β =102.624°. Unit cell volume is 1263.18 Å3.[2]

The molecules have carbon to xenon to carbon bonds in nearly a straight line (the bond angle is at least 175°). The carbon–xenon bond-lengths are 2.35 and 2.39 Å. The two pentafluorophenyl rings are twisted by 72° with respect to each other.[1]

Properties[]

Bis(pentafluorophenyl)xenon decomposes above −20 °C and can explode.[1]

Preparation[]

Bis(pentafluorophenyl)xenon is prepared in liquid dichloromethane at −40 °C.[1] It uses a tetramethyl ammonium fluoride catalyst.[3]

XeF2 + 2(CH3)3SiC6F5 → Xe(C6F5)2 + 2(CH3)3SiF

2C6F5XeF + Cd(C6F5)2 → Xe(C6F5)2 +CdF2

Reactions[]

Bis(pentafluorophenyl)xenon reacts with hydrogen fluoride to form pentafluorophenyl xenon fluoride C6F5XeF.[3] In acetonitrile solution bis(pentafluorophenyl)xenon decomposes to form C6F5-C6F5 (C12F10) and xenon.[3] But in dichloromethane solution the product is mostly pentafluorobenzene.[3]

Bis(pentafluorophenyl)xenon reacts with mercury to make Bis(pentafluorophenyl)mercury.[3]

It reacts with iodine to make pentafluoroiodobenzene. C6F5I.[3]

References[]

  1. ^ a b c d Bock, Harald; Hinz-Hübner, Dirk; Ruschewitz, Uwe; Naumann, Dieter (1 February 2002). "Structure of Bis(pentafluorophenyl)xenon, Xe(C6F5)2". Angewandte Chemie International Edition. 41 (3): 448–450. doi:10.1002/1521-3773(20020201)41:3<448::AID-ANIE448>3.0.CO;2-W.
  2. ^ Bock, H.; Hinz-Hubner, D.; Ruschewitz, U.; Naumann, D. (2002). "CCDC 169453: Experimental Crystal Structure Determination". Cambridge Crystallographic Data Centre. doi:10.5517/cc5pb7d. Cite journal requires |journal= (help)
  3. ^ a b c d e f Frohn, Hermann-Josef; Bardin, Vadim V. (November 2001). "Preparation and Reactivity of Compounds Containing a Carbon−Xenon Bond". Organometallics. 20 (23): 4750–4762. doi:10.1021/om010490j.
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