1965
DOI: 10.1021/j100893a032
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A Study of the Pyrolysis of Methyl Ethyl and Diethyl Carbonates in the Gas Phase

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Cited by 55 publications
(40 citation statements)
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“…Overall, the results presented are in agreement with a previous experimental study on diethyl carbonate pyrolysis, in which also ethene and carbon dioxide were found as products. [9] If monomeric carbonic acid is to be made by twofold ester pyrolysis of carbonates, simple dialkyl carbonates are obviously unlikely to perform well. The following carbonates 4-7 all contain O-X (X = C, N, O) bonds that are weaker than the C-O bond of 2.…”
Section: Diethyl Carbonatementioning
confidence: 99%
“…Overall, the results presented are in agreement with a previous experimental study on diethyl carbonate pyrolysis, in which also ethene and carbon dioxide were found as products. [9] If monomeric carbonic acid is to be made by twofold ester pyrolysis of carbonates, simple dialkyl carbonates are obviously unlikely to perform well. The following carbonates 4-7 all contain O-X (X = C, N, O) bonds that are weaker than the C-O bond of 2.…”
Section: Diethyl Carbonatementioning
confidence: 99%
“…Contrary to TMAH, DMC is neutral, odourless, non-corrosive and nontoxic, and for these appealing properties is a widely investigated methylating reagent in organic synthesis [27,28]. DMC is favourably placed for application in analytical pyrolysis as it is thermally stable [29,30] and its methylating power is favoured at high temperatures [28].…”
Section: Introductionmentioning
confidence: 99%
“…The magnitude of the intramolecular isotope effects and the relative Arrhenius parameters for the two reaction channels have been determined. Our results are compared to previous work on DEC itself [3,4], and the isotope effects in ethyl acetate, ethyl acetate 1,1,2,2-&, and ethyl acetate-ds pyrolyses [5]. …”
Section: I1mentioning
confidence: 75%