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Issue 5, 2017
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Mechanism of activated chemiluminescence of cyclic peroxides: 1,2-dioxetanes and 1,2-dioxetanones

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Abstract

Almost all chemiluminescent and bioluminescent reactions involve cyclic peroxides. The structure of the peroxide and reaction conditions determine the quantum efficiency of light emission. Oxidizable fluorophores, the so-called activators, react with 1,2-dioxetanones promoting the former to their first singlet excited state. This transformation is inefficient and does not occur with 1,2-dioxetanes; however, they have been used as models for the efficient firefly bioluminescence. In this work, we use the SA-CASSCF/CASPT2 method to investigate the activated chemiexcitation of the parent 1,2-dioxetane and 1,2-dioxetanone. Our findings suggest that ground state decomposition of the peroxide competes efficiently with the chemiexcitation pathway, in agreement with the available experimental data. The formation of non-emissive triplet excited species is proposed to explain the low emission efficiency of the activated decomposition of 1,2-dioxetanone. Chemiexcitation is rationalized considering a peroxide/activator supermolecule undergoing an electron-transfer reaction followed by internal conversion.

Graphical abstract: Mechanism of activated chemiluminescence of cyclic peroxides: 1,2-dioxetanes and 1,2-dioxetanones

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Publication details

The article was received on 29 Nov 2016, accepted on 24 Dec 2016 and first published on 03 Jan 2017


Article type: Paper
DOI: 10.1039/C6CP08154A
Citation: Phys. Chem. Chem. Phys., 2017,19, 3955-3962
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    Mechanism of activated chemiluminescence of cyclic peroxides: 1,2-dioxetanes and 1,2-dioxetanones

    F. A. Augusto, A. Francés-Monerris, I. Fdez. Galván, D. Roca-Sanjuán, E. L. Bastos, W. J. Baader and R. Lindh, Phys. Chem. Chem. Phys., 2017, 19, 3955
    DOI: 10.1039/C6CP08154A

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