Seminar by Dr. Soumyadip Mondal (Institute of Science and Technology Austria) on "Individual Marcus-type kinetics controls singlet and triplet oxygen evolution from superoxide."

04 Feb 2026
Seminar Room # 350, second floor annex

Speaker: Dr. Soumyadip Mondal
Institute of Science and Technology Austria
(ISTA)

Title: "Individual Marcus-type kinetics controls singlet and
triplet oxygen evolution from superoxide."

Day and Date: Wednesday, February 04, 2026

Time: 11.00 am.

Venue: Room no. 350, Chemistry Department
Second floor, Annex
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Hosted by Prof. Arnab Dutta

Talk Title : "Individual Marcus-type kinetics controls singlet and triplet oxygen evolution from superoxide."
Abstract
Oxygen evolution from superoxide is a critical aspect of oxygen redox chemistry. Superoxide experiences a broad range of oxidizing conditions to liberate oxygen. A very widely occurring type of oxidation is disproportionation in response to superoxide being highly unstable in most environments1 . This reaction occurs in both protic (aqueous) environments2 and aprotic ones with relatively strong Lewis acids such as Li+ and Na+ 3,4 . During disproportionation (2 O2 – → O2 + O2 2– ), one superoxide is reduced to peroxide while the other is oxidized to form dioxygen, which may be 3O2 or 1O2 5 . Examples include cellular respiration6 and batteries3,7,8. Relative 3O2 and 1O2 yields and kinetics of superoxide disproportionation, and superoxide oxidation more generally, are therefore fundamental to these systems9 . However, it is still unclear what controls the extent to which 1O2 or 3O2 evolves during the oxidation of superoxide to dioxygen. I will talk about our recent findings that the driving force for superoxide oxidation to 3O2 and 1O2 oxygen to be the common descriptor determining the spin state10. This follows individual Marcus normal and inverted region behavior. 1O2 can only become significant since the kinetics for 3O2 evolution slows down in its inverted region. The results help clarify previously inconclusive findings about 1O2 formation from superoxide, including through interaction with chemical oxidants, and proton and Lewis acid-driven disproportionation. Recognizing what controls 3O2 and 1O2 formation from superoxide should enable strategies to suppress 1O2 in human-made redox systems, where 1O2 is, in most cases, harmful. The results expand knowledge on the electrogeneration of excited species more generally11 and pose new open questions, such as the origin of differing maximum kinetics for the ground and excited states. The findings provide insights into understanding and controlling spin states and kinetics in oxygen redox chemistry, with implications for fields including life sciences and energy storage.