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To explore the dynamics of biomolecules, tracing the kinetics of photo‐induced chemical reactions via the triplet excited state (T1) of probe molecules offers a timescale that is about 106 times wider than via the singlet excited state (S1). Using cyclooctatetraene (COT) as a triplet energy acceptor and at the same time as a photostabilizer, the triplet–triplet energy transfer (TTET) kinetics governed...
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