peripheries: facile synthesis, crystallization‐induced blue‐shifted emission, and efficient blue luminogens for non‐doped OLEDS. Journal of Materials Chemistry 22 (24): 12001−12007.20 20 Huang, J., Sun, N., Dong, Y. et al. (2013). Similar or totally different: the control of conjugation degree through minor structural modifications, and deep‐blue aggregation‐induced emission luminogens for non‐doped OLEDS. Advanced Functional Materials 23 (18): 2329−2337.
21 21 Yuan, Y.‐X., Xiong, J.‐B., Luo, J. et al. (2019). The self‐assembly and chiroptical properties of tetraphenylethylene dicycle tetracholesterol with an AIE effect. Journal of Materials Chemistry C 7 (27): 8236–8243.
22 22 Geddes, C. D. and Lakopwicz, J. R. (2005). Advanced Concepts in Fluorescence Sensing. Norwell: Springer.
23 23 Jares‐Erijman, E. A. and Jovin, T. M. (2003). Fret imaging. Nature Biotechnology 21 (11): 1387−1395.
24 24 Liu, Y., Tao, X., Wang, F. et al. (2007). Intermolecular hydrogen bonds induce highly emissive excimers: enhancement of solid‐state luminescence. Journal of Physical Chemistry C 111 (17): 6544−6549.
25 25 An, B.‐K., Lee, D.‐S., Lee, J.‐S. et al. (2000). Microchannel networks for nanowire patterning. Journal of the American Chemical Society 122 (41): 10232−10233.
26 26 Li, Y., Li, F., Zhang, H. et al. (2007). Tight intermolecular packing through supramolecular interactions in crystals of cyano substituted oligo (para‐phenylene vinylene): a key factor for aggregation‐induced emission. Chemical Communications 45 ( 3): 231−233.
27 27 Ren, Y., Kan, W. H., Henderson, M. A. et al. (2011). External‐stimuli responsive photophysics and liquid crystal properties of self‐assembled “phosphole‐lipids”. Journal of the American Chemical Society 133 (42): 17014−17026.
28 28 Xie, Z., Yang, B., Li, F. et al. (2005). Cross dipole stacking in the crystal of distyrylbenzene derivative: the approach toward high solid‐state luminescence efficiency. Journal of the American Chemical Society 127 (41): 14152−14153.
29 29 Zhang, J., Xu, B., Chen, J. et al. (2014). An organic luminescent molecule: what will happen when the “butterflies” come together? Advanced Materials 26 (5): 739−745.
30 30 Yuan, Y.‐X., Wu, B.‐X., Xiong, J.‐B. et al. (2019). Exceptional aggregation‐induced emission from one totally planar molecule. Dyes and Pigments 170: 107556.
31 31 Luo, J., Song, K., Gu, F. et al. (2011). Switching of non‐helical overcrowded tetrabenzoheptafulvalene derivatives. Chemical Science 2 (10): 2029–2034.
32 32 Leung, N. L., Xie, N., Yuan, W. et al. (2014). Restriction of intramolecular motions: the general mechanism behind aggregation‐induced emission. Chemistry–A European Journal, 20 (47): 15349–15353.
33 33 Zhao, Z., Zheng, X., Du, L. et al. (2019). Non‐aromatic annulene‐based aggregation‐induced emission system via aromaticity reversal process. Nature Communications 10 (1): 1–10.
34 34 Yao, L., Zhang, S., Wang, R. et al. (2014). Highly efficient near‐infrared organic light‐emitting diode based on a butterfly‐shaped donor–acceptor chromophore with strong solid‐state fluorescence and a large proportion of radiative excitons. Angewandte Chemie International Edition 53 (8): 2119–2123.
35 35 Liu, J., Meng, Q., Zhang, X. et al. (2013). Aggregation‐induced emission enhancement based on 11, 11, 12, 12,‐tetracyano‐9, 10‐anthraquinodimethane. Chemical Communications 49 (12): 1199–1201.
36 36 Kamaldeep, K. S. n., Kaur, S., Bhalla, V. et al. (2014). Pentacenequinone derivatives for preparation of gold nanoparticles: facile synthesis and catalytic application. Journal of Materials Chemistry A 2 (22): 8369–8375.
37 37 Banal, J. L., White, J. M., Ghiggino, K. P. et al. (2014). Concentrating aggregation‐induced fluorescence in planar waveguides: a proof‐of‐principle. Scientific Reports 4 (1): 1–5.
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.
46 46 Debroy, P., Lindeman, S. V., and Rathore, R. (2009). A versatile synthesis of electroactive stilbenoprismands for effective binding of metal cations. The Journal of Organic Chemistry 74 (5): 2080–2087.
47 47 Sinha, N., Stegemann, L., Tan, T. T. et al. (2017). Turn‐on fluorescence in tetra‐NHC ligands by rigidification through metal complexation: an alternative to aggregation‐induced emission. Angewandte Chemie International Edition 56 (10): 2785–2789.
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.
53 53 Ding, W. L., Peng, X. L., Cui, G. L. et al. (2019). Potential‐energy surface and dynamics simulation of THBDBA: an annulated tetraphenylethene
