1977
DOI: 10.1016/0009-2614(77)85399-2
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Mass spectrometric detection of dioxirane, H2COO, and its decomposition products, H2 and CO, from the reaction of ozone with ethylene

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Cited by 61 publications
(36 citation statements)
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“…The recent paper by Atkinson et al [1982] suggests that the reaction rates of a-and/3-pinene with ozone are lower than previously reported, which would increase the relative importance of the reaction with OH for these two hydrocar-bons. Reaction mechanisms have been investigated in great detail for alkenes [Demerjian et al, 1974;Wadt and Goddard, 1975;Martinez et al, 1977;Herron and Huie, 1977;Niki et al, 1978;Atkinson et al, 1979;Falls and $einfeld, 1978] and to some extent for cyclic olefins [Grosjean, 1977;Grosjean and Friedlander, 1979] and for terpenes [Schwartz, 1974]. The status and limitations of our current knowledge of these reactions have been reviewed by Niki [1978].…”
Section: Tionsmentioning
confidence: 99%
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“…The recent paper by Atkinson et al [1982] suggests that the reaction rates of a-and/3-pinene with ozone are lower than previously reported, which would increase the relative importance of the reaction with OH for these two hydrocar-bons. Reaction mechanisms have been investigated in great detail for alkenes [Demerjian et al, 1974;Wadt and Goddard, 1975;Martinez et al, 1977;Herron and Huie, 1977;Niki et al, 1978;Atkinson et al, 1979;Falls and $einfeld, 1978] and to some extent for cyclic olefins [Grosjean, 1977;Grosjean and Friedlander, 1979] and for terpenes [Schwartz, 1974]. The status and limitations of our current knowledge of these reactions have been reviewed by Niki [1978].…”
Section: Tionsmentioning
confidence: 99%
“…Major products from isoprene photooxidation are formaldehyde and the two unsaturated carbonyls methacrolein and methylvinylketone Arnts and Gay, 1979] The ozone-olefin reaction mechanism is also quite complex and is summarized in Figure 11. It involves ozone addition on the double bond, to form the initial molozonide, and the subsequent formation of a dioxy radical via a dioxirane-type intermediate [Wadt and Goddard, 1975;Martinez et al, 1977]. Further reactions of the dioxy radical lead to a variety of'stable' products (aldehydes, acids) and free radicals.…”
Section: Tionsmentioning
confidence: 99%
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“…Various strategies, methods and many effective catalytic systems have been developed for the preparation of epoxides from olefins [1][2][3][4][5][6][7][8][9][10][11]. Recently, the catalytic epoxidation with organic peroxides, H 2 O 2 , oxygen and air has become an especially attractive target.…”
Section: Introductionmentioning
confidence: 99%
“…Lovas and Suenram (1977) found a number of microwave transitions attributable to an asymmetric top with a large dipole moment. Martinez, Huie and Herron (1977) confFrmed the HgCOg composition by mass spectrometry. The molecular, as opposed to radical, nature of the species was demonstrated by the ability of these researchers to repeatedly freeze and vaporize the intermediate.…”
Section: F Reconciliation Of High Barrier and Experimental Resultsmentioning
confidence: 99%