Abstract
The structural assembly of organic fluorescent molecules exerts a significant influence on solid-state fluorescence properties, including fluorescence tuning and switching. Herein, we have synthesized a Schiff base based organic fluorophore, 2-((E)-((E)-(4-hydroxybenzylidene)hydrazono)(phenyl)methyl)phenol (1), with intra- and intermolecular H-bonding hydroxyl functionalities, and studied its solid state structural arrangement and fluorescence properties. 1 exhibited aggregation induced enhanced emission (AIEE) in the solid state. The crystallization of 1 produced geometrical (E/Z) isomers (1a (E-isomer) and 1b (Z-isomer)) with completely different intra- and intermolecular H-bonding. 1a showed typical intramolecular H-bonding with an adjacent nitrogen and showed six membered planar rings while 1b revealed unusual intramolecular H-bonding with seven membered non-planar rings. The intermolecular H-bonding of the additional hydroxy group in 1a produced a hexagon arrangement with the inclusion of a water molecule whereas a 2D network structure is formed in 1b. However, both 1a and 1b isomers showed large Stokes shifted solid state fluorescence at 570 and 565 nm, respectively, due to the intramolecular H-bonding facilitated excited state intramolecular proton transfer (ESIPT) process. Interestingly, both 1a and 1b exhibited self-reversible fluorescence switching after crushing without showing any structural transformation. 1a exhibited a relatively slow fluorescence recovery compared to 1b. Computational studies showed that intramolecular H-bonding/conformational twisting controlled the electron density distribution in the HOMO. PXRD studies confirmed the structural stability and complete regeneration of the crystalline phase after mechanical crushing. Thus, the simple interplay of intra/intermolecular H-bonding in 1 led to the formation of geometrical isomers with distinct self-reversibility.