cation of mechanical stimuli such as scratching or grinding, promises applications for force sensors. [20][21][22][23][24][25][26][27][28][29][30][31][32][33][34][35][36] Emission changes of coordination complex crystals, [24] polymeric microcrystals, [30] and organic fluorophores, [31][32][33][34][35][36] have been correlated to an applied force or pressure for new anticounterfeiting technologies [23][24][25][26][27][28] and biological stress probes. [29] Force sensing via mechanofluorochromic activity has been reported at the micro/nanoscales by direct measurement of emission changes upon in situ application of varying amounts of mechanical stimulus. [24,30,31,[33][34][35][36] Yet, one issue that remains to be explored is the recovery of the material. Emission changes, correlated with applied force, are induced by morphological changes in the material. This means that subsequent sensing events, after the initial application of force, necessitate recovering the original morphology-a process not so straightforward as this usually requires thermal annealing, [38] solvent fuming, [25,27] or recrystallization. [20][21][22]37] Self-recovery, the spontaneous return to the initial state (of absorption, emission and morphology) of the scratched/ground material under ambient conditions, has been observed in derivatives based on Au(I) complexes, [28] pyrene, [39,40] anthracene, [41,42] tetraphenylethene, [43,44] indolylbenzothiadiazole, [45] triphenylamine, [46] boron-coordinated β-diketonate complexes, [47] and hexathiobenzene. [48] However, many MFC-active materials are left unexplored for multiple-use force sensing applications, not only due to the complexity of instrumentation required for such studies, [24,30,31,[33][34][35][36] but also due to the lack of molecular design leading to reversibility [40] and a clear understanding of mechanism of self-recovery. [30,45] Recently, mechanofluorochromic films based on a family of diphenylamine compounds functionalized with π-extended