Abstract
The bioluminescence reaction of many biological subspecies, most notably fireflies, forms dioxetanone derivatives as high-energy intermediates. The thermal instability of dioxetanones complicates understanding of the transition from the ground state to the first excited state that leads to light emission. Herein, we report the reaction mechanism of 2-coumaranones, synthetically accessible strongly chemiluminescent materials that mimic the bioluminescence reaction. The pathways of chemiexcitation and photorelaxation are clarified on the basis of synthetic evidence and spectrochemical as well as computational mechanistic analysis.
Original language | English (US) |
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Pages (from-to) | 678-681 |
Number of pages | 4 |
Journal | European Journal of Organic Chemistry |
Volume | 2016 |
Issue number | 4 |
DOIs | |
State | Published - Feb 1 2016 |
Keywords
- Bioluminescence
- Luminescence
- Natural products
- Oxygen heterocycles
- Photochemistry
- Reaction mechanisms
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Organic Chemistry