“…8 c To better understand this phenomenon, several synthetic modifications and theoretical calculations were undertaken; the results revealed that the restriction of intramolecular motions, which led to rotation, vibration, and stretching, played a key role in the AIE phenomenon. Several synthetic modifications on organic fluorophores have been developed for AIE materials including siloles, 9 triphenylamine (TPA), 10 cyanostilbenes, 11 tetraphenylethenes, 12 a – d naphthalenediimide 12 e , f and anthracene 13 derivatives, diphenyldibenzofulvenes, 14 BODIPYs, 15 diketopyrrolopyrrole, 16 and fluorene derivatives, 17,18 The enhanced emission of all the AIEgens in their aggregate and solid forms is due to the nonplanar aromatic backbone that restricts the formation of π–π stacking. 5 On the other hand, supramolecular self-assembly of π-conjugated organic fluorescent molecules exhibits the AIE property in the aggregate state.…”