Peroxycarbonates

An MPI-containing peroxycarbonate group was acted with 2,5-dimethyl-2,5-dihydroperoxyhexane or synthesized from diethyleneglycolbis(chloroformate) re- 2,5-dimethyl-2,5-dihydroperoxyhexyne-3 [Eq. (9)] [24]. [Pg.759]

The deoxygenation of peroxycarbonates (53) with phosphines and phosphites has been examined. Reaction with phosphites favours pyrocarbonate formation (Path A) whilst phosphines favour carbonate formation (Path B). Secondary phosphine oxides are oxidized to phosphinic acids by perbenzoic acid. The kinetics of the deoxygenation of hydroperoxides by triphenylphosphine have been examined and the reaction shown to be catalysed by strong acids. ... [Pg.242]

Many other peroxy compounds can analogously be produced in the region of HAP for instance, sodium perborate Na2(B03)2 (from sodium metaborate NaB02) and peroxycarbonates. These compounds are used as stable oxidizing and bleaching agents. [Pg.289]

In practice, promising results have been obtained for several systems. For example, fair to good yields of epoxides are obtained when a two-phase system consisting of alkene and ethyl chloroformate is stirred with a buffered basic solution of hydrogen peroxide. The active oxidant is presumed to be O-ethyl peroxycarbonic acid.85... [Pg.1097]

See entry PEROXYCARBONATE ESTERS See other ALLYL COMPOUNDS... [Pg.988]

See entry THERMAL EXPLOSIONS See other PEROXYCARBONATE ESTERS... [Pg.1007]

The equilibrium between 1,1-dimethylethylperoxyl radicals and 1,1-dimethylethyl tetroxide was first evidenced by Bartlett and Guaraldi [157] for peroxyl radicals generated by irradiation of bis( 1,1-dimethylethyl) peroxycarbonate in CH2C12 at 77 K and oxidation of 1,1-dimethylethyl hydroperoxide with lead tetraacetate at 183 K in CH2C12. A series of studies of this equilibrium were performed later using the EPR technique (see Table 2.12). It is seen that the enthalpy of tetroxide decomposition ranges from 29 to 47 kJ mol-1. [Pg.86]

Bis(fluoroformyl) peroxide, 0625 Bis-3-(2-furyl)acryloyl peroxide, 3640 Bis(trichloroacetyl) peroxide, 1361 Bis(trifluoroacetyl) peroxide, 1367 Diacetyl peroxide, 1537 Dibenzenesulfonyl peroxide, 3499 Dibenzoyl peroxide, 3639 Di-3-camphoroyl peroxide, 3807 Dicrotonoyl peroxide, 2986 Dicyclohexylcarbonyl peroxide, 3667 Didodecanoyl peroxide, 3857 Di-2-furoyl peroxide, 3245 Dihexanoyl peroxide, 3554 Diisobutyryl peroxide, 3032 Diisopropyl peroxydicarbonate, 3034 Dimethanesulfonyl peroxide, 0931 Di-2-methylbutyryl peroxide, 3354 Di-l-naphthoyl peroxide, 3831 3,6-Dioxo-l,2-dioxane, 1445 Dipropionyl peroxide, 2442 Dipropyl peroxydicarbonate, 3035 Di-4-toluenesulfonyl peroxide, 3656 Peroxodisulfuryl difluoride, 4328 Phthaloyl peroxide, 2900 Potassium benzenesulfonylperoxosulfate, 2257 Potassium O-O-benzoylmonoperoxosulfate, 2684 (9-TriIIuoroacctyl-.S -lluorofonny 1 thioperoxide, 1050 See PEROXIDES, PEROXYCARBONATE ESTERS... [Pg.109]

OXOHALOGEN ACIDS, OXYGEN ENRICHMENT 1 -OXYPEROXY COMPOUNDS, OZONIDES PERCHLORYL COMPOUNDS, PEROXOACIDS PEROXOACID SALTS, PEROXYACIDS PEROXYCARBONATE ESTERS, PEROXYESTERS POLYNITROALKYL COMPOUNDS, POLYPEROXIDES QUATERNARY OXIDANTS, TRINITROETHYL ORTHOESTERS XENON COMPOUNDS... [Pg.307]

Of the 3 possible types of peroxycarbonate esters-dialkyl monoperoxycarbonates, dialkyl diperoxycarbonates and dialkyl peroxydicarbonates-, the latter are by far the least stable group. Several of the 16 alkyl and substituted-alkyl esters prepared decomposed violently or explosively at temperatures only slightly above the temperature of preparation (0-10°C), owing to self-accelerating exothermic decomposition. Several were also explosive on exposme to heat, friction or shock [1]. Amines and certain metals cause accelerated decomposition of dialkyl peroxydicarbonates by a true catalytic mechanism [2]. Individually indexed compoimds are ... [Pg.315]

Conditions that permit oxidation of organoboranes to alcohols using molecular oxygen,139 sodium peroxycarbonate,140 or amine oxides141 as oxidants have also been developed. The reaction with molecular oxygen is particularly effective in perfluoroalkane solvents.142... [Pg.233]

The IR and Raman spectra of esters derived from peroxycarboxylic and peroxycarbonic esters show a band near 860 cm, assigned to a stretching mode of the OO gronp. The band of the carbonyl gronp in these componnds is shifted to higher frequencies by 30-40 cm , as compared to ordinary esters . ... [Pg.705]

Bis(trifluoromethyl) peroxycarbonate, 705 Bis(trifluoromethyl) peroxydicarbonate, 705 Bis(trifluoromethyl) trioxide IR spectrum, 740 O NMR spectroscopy, 182 Bis(trifluoromethyl) tiioxydicarbonate, 740 Bis(trimethylsilyl) monoperoxysulfate Baeyer-Vilhger oxidation, 785 catalytic epoxidation, 791-2 Bis(trimethylsilyl) peroxide (BTSP) alcohol oxidation, 787-90 alkyne reactions, 800 aromatic compounds, 794-5 Baeyer-Vilhger ketone oxidation, 784-7 demethylation, 798... [Pg.1446]

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