Xenon, compounds

Xenon arc lamp Xenon compounds Xenon dichloride Xenon difluoride... 

Halides. Xenon duorides, xenon oxide tetraduoride [13774-85-1XeOE, and their complexes are the only thermodynamically stable xenon compounds. Xenon diduo ride [13709-36-9] xenon tetraduoride [13709-61-0], and xenon hexaduoride [13693-09-9] are colodess, crystalline soHds which can be sublimed under vacuum at 25°C. The mean thermochemical bond energies are XeE2, 132.3 0.7 kJ/mol (31.6 0.2 kcal/mol) XeE ... 

The starting point for the synthesis of xenon compounds is the preparation of xenon difluoride, XeF2, and xenon tetrafluoride, XeF4, by heating a mixture of the elements to 400°C at 6 atm. At higher pressures, fluorination proceeds as far as xenon hexafluoride, XeFfi. All three fluorides are crystalline solids (Fig. 15.27). In the gas phase, all are molecular compounds. Solid xenon hexafluoride, however, is ionic, with a complex structure consisting of XeF< + cations bridged by F anions. 

Xenon(II) fluoride trifluoroacetate [25710-89-8] F3CCO.OXeF Jha. N. K RICRev., 1971, 4, 157 It explodes on thermal or mechanical shock. See other XENON compounds C2F402Xe... 

See other XENON compounds, See also quaternary oxidants... 

Liquid mixtures of the 2 xenon compounds, cooled in liquid nitrogen, tend to flash, then explode after a few seconds. 

See other NON-METAL HALIDES, oxidants, xenon compounds... 

See other xenon compounds See related non-metal oxides... 

See Other NON-METAL OXIDES, OXIDANTS, XENON COMPOUNDS... 

Since the discovery of the first noble gas compound, Xe PtF (Bartlett, 1962), a number of compounds of krypton, xenon, and radon have been prepared. Xenon has been shown to have a very rich chemistry, encompassing simple fluorides, XeF2> XeF, and XeF oxides, XeO and XeO oxyf luorides, XeOF2> XeOF, and Xe02 2 perxenates perchlorates fluorosulfates and many adducts with Lewis acids and bases (Bartlett and Sladky, 1973). Krypton compounds are less stable than xenon compounds, hence only about a dozen have been prepared KrF and derivatives of KrF2> such as KrF+SbF, KrF+VF, and KrF+Ta2F11. The chemistry of radon has been studied by radioactive tracer methods, since there are no stable isotopes of this element, and it has been deduced that radon also forms a difluoride and several complex salts. In this paper, some of the methods of preparation and properties of radon compounds are described. For further information concerning the chemistry, the reader is referred to a recent review (Stein, 1983). 

This behavior provides evidence that in each of the compounds, radon is in the +2 oxidation state When higher-valent xenon compounds, such as XeF and XeF, are hydrolyzed, water-soluble xenon species (XeO and XeO ) are produced (Malm and Appelman, 1969). We have observed no radon species corresponding to these xenon species in hydrolysis experiments. 

Russian scientists (Avrorin et al., 1981, 1985) have reported that reactions of complex mixtures of radon, xenon, metal fluorides, bromine pentafluoride, and fluorine yield a higher fluoride of radon which hydrolyzes to form RnO. However, efforts to confirm these findings have been unsuccessful. In similar experiments which have been carried out at Argonne National Laboratory (Stein, 1984), it has been found that radon in the hydrolysate is merely trapped in undissolved solids centrifugation removes the radon from the liquid phase completely. This is in marked contrast to the behavior of a solution of XeO, which can be filtered or centrifuged without loss of the xenon compound. Hence there is no reliable evidence at present for the existence of a higher oxidation state of radon or for radon compounds or ions in aqueous solutions. Earlier reports of the preparation of oxidized radon species in aqueous solutions (Haseltine and Moser, 1967 Haseltine, 1967) have also been shown to be erroneous (Flohr and Appelman, 1968 Gusev and Kirin, 1971). 

Numerous other reactions of krypton difluoride are known, but they will not be reviewed here. The chemistry of krypton is well established, but it is still much less extensive than that of xenon. Although a rather extensive chemistry of the noble gases has developed, the vast majority of the studies have dealt with the xenon compounds. 

In 2001-2002, comprehensive reviews (6-8) on the preparation and reactivity of carbon-xenon compounds have been published covering the literature until 2000-2001. The objective of this chapter is to highlight the progress that was achieved during the first decade, to discuss more recent progress, and to identify areas that are open for further investigation. 

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