Dioxetane intermediates readily decompose to chemiluminescent triplet carbonyls, giving rise what has been paradoxically called photochemistry in the dark. In this issue of Photochemistry and Photobiology, Bechara et al. report on mechanistic advances such a reaction. With use horseradish peroxidase for isobutyraldehyde-derived acetone, light emission from acetone singlet oxygen can be quenched...