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• Synthesis of AIEgens with unsymmetrical intramolecular H-bonding functionalities. • Large Stoke shifted emission in the solid-state by ESIPT process. • Molecular structure dependent self-assembly, fluorescence efficiency and tunable emission. • Highly reversible mechanofluorochromism. We have synthesized two new ESIPT fluorophores (1-((E)-((E)-((2-hydroxyphenyl)(phenyl)methylene)hydrazono)methyl) naphthalen-2-ol (Naph-2-OH) and 5-(diphenylamino)-2-((E)-((E)-((2-hydroxyphenyl)(phenyl) methylene)hydrazono)methyl) phenol (TPA-2-OH)) with two unsymmetrical intramolecular H-bonding functionalities and investigated the solid-state structural assembly and fluorescence properties. The crystal structure analysis confirmed the formation of strong intramolecular H-bonding and twisted molecular conformation. The nonplanar twisted molecular conformation produced well separated molecules in the crystal lattice that lead to strongly enhanced emission ((λ max = 538 nm, Φ f = 5.2% (Naph-2-OH), λ max = 562 nm, Φ f = 13.4% (TPA-2-OH)). Density functional theoretical (DFT) calculation supported the fluorescence tuning and intramolecular charge transfer (ICT) from TPA donor to imine acceptor. Both Naph-2-OH and TPA-2-OH showed mechanical crushing and heating induced reversible fluorescence switching due to the reversible phase transformation between crystalline and amorphous state. ESIPT fluorophores with two unsymmetrical intramolecular H-bonding exhibited structure dependent molecular packing, solid state fluorescence and mechanofluorochromism. [Display omitted] [ABSTRACT FROM AUTHOR]