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Chemiluminescence of o-Dicarboxylic Acid Chlorides

According to this suggestion there exists an equilibrium between the normal six-membered ring phthaloylperoxide (24 a) and its phthalide isomer -analogous to that of the corresponding diacyl chlorides. [Pg.45]

The isomer can be readily isolated, and actually gives rise to chemiluminescence in the presence of Na202 and an appropriate fluorescer [27]. Dioxiranes and dioxiranone (29) have been described recently [28]. It is assumed that the isophthaloylperoxide (28) is transformed to phthalic anhydride by transfer of an oxygen atom to the fluorescer. [Pg.45]

Further investigations are necessary to confirm this very interesting new suggestion. [Pg.45]

The essential differences between the two forms of peroxide reaction can be seen in the following comparison  [Pg.45]

With PPO and BPEA concentration = lxlO 0cLis ca. 2Ox0clDPO/BPEA in the same concentrations [Pg.45]


See other pages where Chemiluminescence of o-Dicarboxylic Acid Chlorides is mentioned: [Pg.45]    [Pg.45]   


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