Non-Adabatic Chemiluminescent Dynamics of the Methyl-Substituted 1,2-Dioxetanes*

That the origin of chemi- and bioluminescence is a non-adiabatic process originating from the breakage of a peroxide bond is well understood. However, some details in the mechanisms of chemi- and bioluminescence are not well understood. In this lecture we will unravel one of these lesser understood experimental observations. That is, the intriguing and dramatic increase - 0.003 to 0.35 - of the quantum yield of the phosphorescence for the series of 1,2-dioxetane molecules substituted going from none up to four methyl groups. This changes of quantum yield, more than two orders of magnitude, is studied in a series of non-adiabatic surface hopping dynamics simulations using multi-configurational electron structure theory. The dynamics reveal how the seemingly innocent methyl groups retards the dynamic of the fragmentation process - 1,2-dioxetane thermally fragments to two formaldehyde - in a so-called entropic trap, there by enhancing the interstate crossing efficiency. The lecture will initially give a brief background to the field of chemi- and bioluminescence, followed by the details for the problem and simulations listed above.