Most of aromatic conjugated imines I know are far less fluorescent than its aromatic precursor. What happens to the excited state when the imine is formed?
Can you provide some example structures of the products and the precursors?
Please insert your question in google
Why aromatic imines are weakly fluorescent?
and you will obtain a lot of hints.
Among them :
https://www.researchgate.net/topic/Imines
Please read them and good luck
JRG
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