Xenon oxide difluoride

Xenon Oxide Difluoride. XeOF2 mw 185.20 bright yel solid mp —25° to —15° (decompn occurs on slow warming, warming at > 20°/hr leads to expin). Prepn is by co-condensation of w and Xe tetrafluoride under vac at —196°, wanning to —80° and then to —63° for 2 hrs, and finally to -47° for 1 hr. The compd explds in contact with Sb pentafluoride or As pentafluoride at —196°, also when in contact with solid Hg... 

The pure, crystalline chromium (V) oxide trifluoride can be prepared by the reaction of xenon(II) difluoride and chromium (VT) dioxide difluoride [7788-96-7], also known as chromyl fluoride, Cr02F2 (56) ... 

Although uncontrolled reaction of xenon hexafluoride and moisture produces explosive xenon trioxide, controlled action by progressive addition of limited amounts of water vapour with agitation to a frozen solution of the hexafluoride in anhydrous hydrogen fluoride at —196° C to give xenon oxide tetrafluoride or xenon dioxide difluoride is safe [1], Controlled hydrolysis in solution in hydrogen fluoride is, however, described as hazardous [2],... 

The Compound XeF XeOFj. Xenon oxide tetrafluoride ) was vacuum distilled on to xenon difluoride(0.67 mmole) contained in a KelF weighing bottle, of lO ml capacity, provided with a KelF valve. Excess XeOF was removed under vacuum with the bottle and its contents at 0°C. The white solid residue, m.p. 29 °C corresponded to an XeOF uptake (0.67 mmole) commensurate with the composition XeFj XeOF. ... 

In view of the instability of the trioxide it is interesting to speculate on the stability of the oxyfluorides. Xenon oxide tetrafluoride should be an exothermic compound since the atomic heat of formation using average bond energies of 32 kcal. and 17 kcal. respectively for Xe-F and Xe-O is —160 kcal. mole-. The combined heat of atomization of four fluorine atoms (4 x 18.3 kcal.) and one oxygen atom (59.2 kcals.), 132.4 kcal., is less than this. Xenon dioxide difluoride, by such considerations, should be endothermic. It is of interest that xenon oxide tetrafluoride is easily made by controlled hydrolysis of xenon hexafluoride and is a thermally stable entity (m.p. —28) whereas xenon dioxide difluoride has been observed only mass spectrometrically < >. 

Shortly after publication of the observations on the synthesis of xenon tetrafluoride, research was initiated with the noble gases in a number of laboratories. Xenon difluoride, xenon hexafluoride, xenon oxide tetrafluoride, and xenon trioxide were synthesized and reasonably well characterized within a rather short time. A number of other compounds have since been isolated, including xenon tetraoxide, a family of perxenates, and a variety of complex fluorides such as XeF2-2SbF5, XeFe BFs, and CsjXeFs. 

Xenon difluoride dissolves in water, yielding a solution which contains undissociated XeFa molecules which have a half-life of about 7 hours at 0°. It eventually hydrolyzes to yield the expected products, xenon, hydrogen fluoride, and oxygen. The hydrolysis reactions of the tetrafluoride and hexafluoride are somewhat more complicated. The addition of the stoichiometric amount of water to the hexafluoride results in the formation of xenon oxide tetrafluoride. Hydrolysis of either fluoride with an excess of water or acid yields in solution a stable xenon(VI) species, which has been shown to be hydrated xenon trioxide. Removal of the excess water leaves xenon trioxide as a solid residue. Inasmuch as this solid is an extremely sensitive explosive, such solutions must be handled with care. 

IV) oxide sulfate (III) sulfate (III) sulfide Xenon difluoride hexafluoride tetrafluoride trioxide Ytterbium... 

Silver difluoride [7783-95-1], AgF2, is a black crystalline powder. It has been classified as a hard fluorinating agent (3) which Hberates iodine from KI solutions and o2one from dilute aqueous acid solutions on heating. It spontaneously oxidizes xenon gas to Xe(II) in anhydrous hydrogen fluoride solutions (20). 

Stable noble-gas compounds have no industrial uses as of this writing but are frequently utilized in laboratories as fluorinating and oxidizing agents. Xenon difluoride and xenon tetrafluoride are relatively mild oxidative fluorinating agents and have been used for the preparation of phosphoms, sulfur, tellurium. 

Trimethylarsine gives a 98% yield of trimethylarsine difluoride when treated with xenon difluoride [102] in fluorotrichloromelhane. and tnsfpentafluorophen-yl)arsine gives a 94% yield of tris(pentafluornphenyl)arsme difluoride after reaction with dilute fluorine in fluorotnchloromethane at 0 C [106] Other trivalent arsenic compounds have also been fluorinated with xenon difluoride [103] In addition, arsines have been oxidatively fluorinated by iodine pentafluoride [107] or electrochemically in 26-34% yield [108]... 

Xenon difluoride has been used to oxidize a number of antimony compounds [102, 109] in yields ranging from 73 to 98%. Elemental fluorine oxidized tris(pen-tafluorophenyl)stibine to tris(pentafluorophenyl)stibine difluoride in 98% yield [706]. Oxidative fluonnation of stibines has also been accomplished with iodine pentafluoride [707]. 

Pentafluorophenylditelluridc yields 79-80% pentafluorophenyltellunum tri fluoride on treatment with fluorine or xenon difluoride [105] The fluonnated tetravalent tellurium can be further oxidized to hexavalent tellurium with either xenon difluoride [/22] or fluorine [123]... 

Polymer-bound phenyliodine difluoride, which also has been used as a reagent to add fluorine to alkenes, can be prepared by the addition of xenon difluoride to the polymer [134, 135 136] Methyl iodide is converted to trifluoro methyliodine difluoride by treatment with fluorine at -110 C [137] Perfluoro-alkyliodine tetrafluorides could be synthesized from the perfluoroalkyliodine difluorides and fluorine [138] or chlorine trifluoride [139] Perfluoroalkyl [140] and perfluoroaryl [141] iodides are oxidized to the corresponding iodine difluorides by chlorine trifluoride. 

On the other hand, oxidizing fluonnating agents like silver difluoride, xenon difluoride, or bromine trifluoride replace one chlorine group and then cleave the sulfur-nitrogen bond [56],... 

Though a powerful oxidant, the difluoride is not explosively unstable. Safe procedures for the use of xenon difluoride in fluorination reactions are detailed. Residual traces of the fluoride are rapidly destroyed by dichloromethane at ambient temperatures. 

In the preparation of xenon difluoride dioxide from caesium nitrate and xenon tetrafluoride oxide, the latter must always be used in excess to prevent formation of explosive xenon trioxide. 

In the reaction of the pentaoxide with xenon tetrafluoride oxide to give xenon difluoride dioxide and nitryl fluoride, the xenon tetrafluoride oxide must be used in excess to avoid formation of xenon trioxide, which forms a sensitive explosive mixture with xenon difluoride dioxide. 

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