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Oxides carbonyl difluoride

Oxygen difluoride reacts rapidly with selected alkenes at low temperatures however, per-fliioroalkenes are less reactive than the corresponding alkylalkenes and require either thermal or ultraviolet activation." The oxidation, which is a homogeneous chain reaction," of hexa-fluoropropene, tetrafluorocyclopropene, and pcrfluorobut-2-ene all give a variety of products such as carbon tetrafluoridc, carbonyl difluoride, hexafluoroethane, oxiranes, and other oxidation products." This reaction is not useful for preparative organic work. [Pg.697]

SYNS CARBON DIFLUORIDE OXIDE CARBON FLUORIDE OXIDE CARBONIC DIFLUORIDE CARBON OXYFLUORIDE CARBONYL DIFLUORIDE DIFLUOROFORMALDEHYDE FLUOPHOSGENE FLUOROFORMYL FLUORIDE FLUOROPHOSGENE RCRA WASTE NUMBER U033... [Pg.291]

Carbonyl difluoride is usually the major product of the oxidation of tetrafluoroethene, CFj=CF3, whether the oxidation is induced thermally, photochemically or by ionising radiation. [Pg.577]

Carbonyl difluoride is the principal product of the oxidation of tetrafluoroethene by molecular oxygen, whether induced thermally, photolytically, or by ionizing (X-ray or y-ray) radiation. A comparison of the methods has been carried out for the gas phase in a static system, and the results are summarized in Table 13.2 [320]. Tetrafluoroethene oxide, CjF O (13.2), and hexafluorocyclopropane, (CF2)3 (13.3), are formed as additional gaseous products... [Pg.578]

Carbonyl difluoride is formed frequently during the oxidation of many fluorine-containing halocarbons. The "simplest" fluorocarbon, CFj (prepared from the decomposition of trifluoromethyl fluorophosphoranes), when generated at 100 C in the presence of Oj, gives COFj [1299]. [Pg.583]

The oxidation of haiogenated methanes by SO 3 is particuiariy worthy of mention. By choice of the halogen substituents, each of the more common carbonyl dihalides, both symmetrical and asymmetrical, can be prepared by a convenient laboratory method. For the synthesis of carbonyl difluoride, the reagents CF Clj or CF Br may be used. The addition of CFjBtj (0.5 mol) to SO 3 (2.5 mol) at 35-44 C over 2 h resulted in a yield (based on CFjBrj) of COFj of 63 %, according to [1875] ... [Pg.588]

Fluorination of high molecular weight polyethers with elemental fluorine (diluted with helium) at room temperature gave fluorinated polyethers, which were depolymerized by further treatment with flowing F -He at 55-210 "C to produce carbonyl difluoride, amongst the decomposition products [1197c]. COFj is also formed in the oxidative thermal degradation of polyethers derived from hexafluoropropene oxide [1582]. Polymeric C F Oj decomposes, at an unspecified temperature, into carbonyl difluoride [760], The presence of... [Pg.596]

Carbonyl difluoride will react with partially oxidized charcoals to produce graphite fluorides, containing up to 10% fluoride [ICI29]. Treatment of carbonyl difluoride with carbon monoxide at temperatures in excess of 350 C and elevated pressures, and in the presence of a catalyst e.g. Fe or CuFj), is reported to generate tetrafluoroethene [842] ... [Pg.630]

Carbonyl difluoride has been used as a plasma etchant for silicon, and was found to etch the surface rapidly [397]. A CF -Oj plasma etchant has also been used COFj is formed as a primary oxidation product [153]. An excess of O, in the plasma causes loss of COF 2 by reaction with singlet oxygen (vide infra), with a concomitant drop in the formation of SiF [153]. COF2 will also thermally (625 C) etch Si(lll) surfaces, and photochemically... [Pg.633]

Bis(trifluoromethyl)carbene, from bis(trifluoromethyl)(liazirine, reacts with carbonyl difluoride at 180 C over 4 h in a sealed tube, to give a yield (40%) of the adduct, perfluoroisobutene oxide, along with hexafluoropropanone (10%) [1300] ... [Pg.642]


See other pages where Oxides carbonyl difluoride is mentioned: [Pg.300]    [Pg.301]    [Pg.578]    [Pg.584]    [Pg.640]   
See also in sourсe #XX -- [ Pg.629 ]




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Carbonyl difluoride

Carbonyl oxidation

Carbonyl oxide

Carbonylation oxide

Metal oxides reaction with, carbonyl difluoride

Oxidation carbonylative

Oxidation oxidative carbonylation

Oxidative carbonylation

Oxidative carbonylations

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