“…In 2012, Wang et al [ 43 ] obtained a family of D-A-D type NIR fluorophores (4,9-Bis[4-(1,2,2-triphenylvinyl)phenyl][1,2,5]thiadiazolo-[3,4-g]-quinoxaline ( M19 ), 4,9-Bis{4-[2,2-bis(4-methoxyphenyl)-1-phenylvinyl]phenyl}[1,2,5]thiadiazolo-[3,4-g]quinoxaline ( M20 ), 4,8-Bis[4-(1,2,2-triphenylvinyl)phenyl]benzo[1,2-c:4,5-c′]bis-[1,2,5]thiadiazole ( M21 ) and 4,8-Bis{4-[2,2-bis(4-methoxyphenyl)-1-phenylvinyl]phenyl}benzo-[1,2-c:4,5-c′]bis[1,2,5]thiadiazole ( M22 )) containing rigid nonplanar conjugated tetraphenylethene (TPE) moieties with electron-deficient [1,2,5]thiadiazolo[3,4-g]quinoxaline (QTD) or BBTD as acceptors ( Figure 10 ). A twisted TPE had the excellent aggregation-induced emission enhancement (AIEE) and showed a higher fluorescence efficiency in the solid state than in solution [ 111 , 112 , 113 ]. So incorporation of TPE units into the chemical structures of poor fluorophores could improve their fluorescence efficiency in the solid state significantly.…”