Abstract
Multistimuli-responsive chromism was observed for vinylene-linked bisflavin 1 a with an extended π-conjugated platform. The yellow emission of a dilute solution of 1 a in CHCl3 (0.2 mM) observed at 298 K under UV excitation was changed to orange or red emission upon (1) an increase of concentration, (2) a decrease of temperature, and (3) variation of the solvent. This is in contrast to the almost non stimuli-responsive chromism of the N-methylated bisflavin analogue 1 b and monoflavin 2 a. Mechanistic investigation by 1 H NMR analysis under various conditions revealed that the extended π-conjugation platform and imide moiety of 1 a generate controllability in the formation of lower- and higher-ordered aggregates, which induce variation of the emission color upon change. Bisflavin 1 a also exhibited redox-induced chromism, where the orange emission of 1 a was quenched by the addition of hydrazine under anaerobic conditions, and changed back to the original emission upon subsequent bubbling of O2 gas.
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