Handbook of Aggregation-Induced Emission, Volume 1

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38 38 Irie, M., Fukaminato, T., Matsuda, K. et al. (2014). Photochromism of diarylethene molecules and crystals: memories, switches, and actuators. Chemical Reviews 114 (24): 12174–12277.

39 39 Yuan, Y. X. and Zheng, Y. S. (2019). New acylhydrazone photoswitches with quantitative conversion and high quantum yield but without hydrogen bond stabilizing (Z)‐isomer. ACS Applied Materials & Interfaces 11 (7): 7303–7310.

40 40 Tseng, N. W., Liu, J., Ng, J. C. et al. (2012). Deciphering mechanism of aggregation‐induced emission (AIE): Is E–Z isomerisation involved in an AIE process? Chemical Science 3 (2): 493–497.

41 41 Wang, J., Mei, J., Hu, R. et al. (2012). Click synthesis, aggregation‐induced emission, E/Z isomerization, self‐organization, and multiple chromisms of pure stereoisomers of a tetraphenylethene‐cored luminogen. Journal of the American Chemical Society 134 (24): 9956–9966.

42 42 Yang, Z., Qin, W., Leung, N. L. et al. (2016). A mechanistic study of AIE processes of TPE luminogens: intramolecular rotation vs. configurational isomerization. Journal of Materials Chemistry C 4 (1): 99–107.

43 43 Xiong, J.‐B., Feng, H.‐T., Sun, J.‐P. et al. (2016). The fixed propeller‐like conformation of tetraphenylethylene that reveals aggregation‐induced emission effect, chiral recognition, and enhanced chiroptical property. Journal of the American Chemical Society 138 (36): 11469–11472.

44 44 Xiong, J.‐B., Yuan, Y.‐X., Wang, L. et al. (2018). Evidence for aggregation‐induced emission from free rotation restriction of double bond at excited state. Organic Letters 20 (2): 373–376.

45 45 Yuan, Y.‐X., Zhang, H.‐C., Hu, M. et al. (2020). Enhanced DNA sensing and chiroptical performance by restriction of double‐bond rotation of AIE cis‐tetraphenylethylene macrocycle diammoniums. Organic Letters 22: 1836–1840.

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48 48 Zeng, F., Zhao, S., Jiang, Y. et al. (2017). An emissive rigid tetraphenylethylene‐based molecule and its thermal polymerization. Tetrahedron 73 (30): 4487–4492.

49 49 Qian, H., Cousins, M. E., Horak, E. H. et al. (2017). Suppression of Kasha's rule as a mechanism for fluorescent molecular rotors and aggregation‐induced emission. Nature Chemistry 9 (1): 83–87.

50 50 Kokado, K. and Sada, K. (2019). Consideration of molecular structure in the excited state to design new luminogens with aggregation‐induced emission. Angewandte Chemie 131 (26): 8724–8731.

51 51 Peng, X.‐L., Ruiz‐Barragan, S., Li, Z.‐S. et al. (2016). Restricted access to a conical intersection to explain aggregation induced emission in dimethyl tetraphenylsilole. Journal of Materials Chemistry C 4 (14): 2802–2810.

52 52 Crespo‐Otero, R., Li, Q., and Blancafort, L. (2019). Exploring potential energy surfaces for aggregation‐induced emission—from solution to crystal. Chemistry–An Asian Journal 14 (6): 700–714.