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In this work, we address a mechanistic issue on AIE process and correct a long-held misconception on stilbene photoluminescence. E–Zisomerisation has been generally recognized as the cause of emission quenching in stilbene solutions. A natural question arisen from this common belief is whether suppression of E–Zisomerisation by aggregate formation in a stilbenic fluorogen system is responsible for its AIE phenomenon. Monitoring of the structural change of a stilbene derivative named 1,2-diphenyl-1,2-di(p-tolyl)ethene by NMR during UV irradiation reveals that the E–Zisomerisation is not involved in its AIE process under the normal photoluminescence spectral measurement conditions.
Tseng et al. (Thu,) studied this question.