A salicylaldehyde azine-based derivative, which exhibited switchable solid-state fluorescence in response to external thermal and mechanical grinding stimulus, was reported in this study. Diffuse reflectance solid-state spectroscopy, fluorescence spectroscopy, solid-state 13 C and 1 H NMR spectroscopy, single crystal XRD analyses, powder X-ray diffractometry, and differential scanning calorimetry were used for investigating the changes of molecular packing modes. The multistimuli fluorescence originated from two distinctive crystalline lattices via different π–π interactions. The local dipole coupling among molecules with donor–planar–acceptor structure was evidenced to be the essential factor for the effective solid luminescence-switching properties.
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Chen et al. (2011) studied this question.
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