Handbook of Aggregation-Induced Emission, Volume 1. Группа авторов

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aggregation‐induced emission system via aromaticity reversal process. Nat. Commun. 10 (1), 2952.

      44 44 Bu, F.; Duan, R.; Xie, Y.; Yi, Y.; Peng, Q.; Hu, R.; Qin, A.; Zhao, Z.; Tang, B. Z. (2015). Unusual aggregation‐induced emission of a coumarin derivative as a result of the restriction of an intramolecular twisting motion. Angew. Chem. Int. Ed. 54 (48), 14492–14497.

      45 45 Yu, G.; Yin, S.; Liu, Y.; Chen, J.; Xu, X.; Sun, X.; Ma, D.; Zhan, X.; Peng, Q.; Shuai, Z.; Tang, B.; Zhu, D.; Fang, W.; Luo, Y. (2005). Structures, electronic states, photoluminescence, and carrier transport properties of 1,1‐disubstituted 2,3,4,5‐tetraphenylsiloles. J. Am. Chem. Soc. 127 (17), 6335–6346.

      46 46 Tang, B. Z.; Zhan, X.; Yu, G.; Sze Lee, P. P.; Liu, Y.; Zhu, D. (2001). Efficient blue emission from siloles. J. Mater. Chem. 11 (12), 2974–2978.

      47 47 Zhao, E.; Lam, J. W. Y.; Hong, Y.; Liu, J.; Peng, Q.; Hao, J.; Sung, H. H. Y.; Williams, I. D.; Tang, B. Z. (2013). How do substituents affect silole emission? J. Mater. Chem. C 1 (36), 5661–5668.

      48 48 Zhao, Z.; Liu, D.; Mahtab, F.; Xin, L.; Shen, Z.; Yu, Y.; Chan, C. Y. K.; Lu, P.; Lam, J. W. Y.; Sung, H. H. Y.; Williams, I. D.; Yang, B.; Ma, Y.; Tang, B. Z. (2011). Synthesis, structure, aggregation‐induced emission, self‐assembly, and electron mobility of 2,5‐bis(triphenylsilylethynyl)‐3,4‐diphenylsiloles. Chem. Eur. J. 17 (21), 5998–6008.

      49 49 Zhan, X.; Haldi, A.; Risko, C.; Chan, C. K.; Zhao, W.; Timofeeva, T. V.; Korlyukov, A.; Antipin, M. Y.; Montgomery, S.; Thompson, E.; An, Z.; Domercq, B.; Barlow, S.; Kahn, A.; Kippelen, B.; Brédas, J.‐L.; Marder, S. R. (2008). Fluorenyl‐substituted silole molecules: geometric, electronic, optical, and device properties. J. Mater. Chem. 18 (26), 3157–3166.

      50 50 Romanov, A. S.; Di, D.; Yang, L.; Fernandez‐Cestau, J.; Becker, C. R.; James, C. E.; Zhu, B.; Linnolahti, M.; Credgington, D.; Bochmann, M. (2016). Highly photoluminescent copper carbene complexes based on prompt rather than delayed fluorescence. Chem. Commun. 52 (38), 6379–6382.

      51 51 Karadakov, P. B. (2008). Aromaticity and antiaromaticity in the low‐lying electronic states of cyclooctatetraene. J. Phys. Chem. A 112 (49), 12707–12713.

      52 52 Feixas, F.; Vandenbussche, J.; Bultinck, P.; Matito, E.; Solà, M. (2011). Electron delocalization and aromaticity in low‐lying excited states of archetypal organic compounds. Phys. Chem. Chem. Phys. 13 (46), 20690–20703.

      53 53 Gogonea, V.; Schleyer, P. v. R.; Schreiner, P. R. (1998). Consequences of triplet aromaticity in 4nπ‐electron annulenes: calculation of magnetic shieldings for open‐shell species. Angew. Chem. Int. Ed. 37 (13‐14), 1945–1948.

      54 54 Dong, Y.; Xu, B.; Zhang, J.; Lu, H.; Wen, S.; Chen, F.; He, J.; Li, B.; Ye, L.; Tian, W. (2012). Supramolecular interactions induced fluorescent organic nanowires with high quantum yield based on 9,10‐distyrylanthracene. CrystEngComm 14 (20), 6593–6598.

      55 55 Qin, A.; Lam, J. W. Y.; Mahtab, F.; Jim, C. K. W.; Tang, L.; Sun, J.; Sung, H. H. Y.; Williams, I. D.; Tang, B. Z. (2009). Pyrazine luminogens with “free” and “locked” phenyl rings: understanding of restriction of intramolecular rotation as a cause for aggregation‐induced emission. Appl. Phys. Lett. 94 (25), 253308.

      56 56 Chen, J.; Xu, B.; Ouyang, X.; Tang, B. Z.; Cao, Y. (2004). Aggregation‐induced emission of cis,cis‐1,2,3,4‐tetraphenylbutadiene from restricted intramolecular rotation. J. Phys. Chem. A 108 (37), 7522–7526.

      57 57 Wu, Q.; Zhang, T.; Peng, Q.; Wang, D.; Shuai, Z. (2014). Aggregation induced blue‐shifted emission ‐ the molecular picture from a QM/MM study. Phys. Chem. Chem. Phys. 16 (12), 5545–5552.

      58 58 Heller, E. J.; Sundberg, R.; Tannor, D. (1982). Simple aspects of Raman scattering. J. Phys. Chem. 86 (10), 1822–1833.

      59 59 Santoro, F.; Cappelli, C.; Barone, V. (2011). Effective time‐independent calculations of vibrational resonance Raman spectra of isolated and solvated molecules including Duschinsky and Herzberg–Teller effects. J. Chem. Theory Comput. 7 (6), 1824–1839.

      60 60 Dong, Y.; Lam, J. W. Y.; Qin, A.; Sun, J.; Liu, J.; Li, Z.; Sun, J.; Sung, H. H. Y.; Williams, I. D.; Kwok, H. S.; Tang, B. Z. (2007). Aggregation‐induced and crystallization‐enhanced emissions of 1,2‐diphenyl‐3,4‐bis(diphenylmethylene)‐1‐cyclobutene. Chem. Commun. ( 31), 3255–3257.

      61 61 Zhang, T.; Ma, H.; Niu, Y.; Li, W.; Wang, D.; Peng, Q.; Shuai, Z.; Liang, W. (2015). Spectroscopic signature of the aggregation‐induced emission phenomena caused by restricted nonradiative decay: a theoretical proposal. J. Phys. Chem. C 119 (9), 5040–5047.

      62 62 Lin, S. H.; Bersohn, R. (1968). Effect of partial deuteration and temperature on triplet‐state lifetimes. J. Chem. Phys. 48 (6), 2732–2736.

      63 63 Saltiel, J.; Waller, A. S.; Sears, D. F.; Garrett, C. Z. (1993). Fluorescence quantum yields of trans‐stilbene‐d0 and ‐d2 in n‐hexane and n‐tetradecane: medium and deuterium isotope effects on decay processes. J. Phys. Chem. 97 (11), 2516–2522.

      64 64 Zhang, T.; Peng, Q.; Quan, C.; Nie, H.; Niu, Y.; Xie, Y.; Zhao, Z.; Tang, B. Z.; Shuai, Z. (2016). Using the isotope effect to probe an aggregation induced emission mechanism: theoretical prediction and experimental validation. Chem. Sci. 7 (8), 5573–5580.

      65 65 Chen, J.; Xu, B.; Yang, K.; Cao, Y.; Sung, H. H. Y.; Williams, I. D.; Tang, B. Z. (2005). Photoluminescence spectral reliance on aggregation order of 1,1‐bis(2′‐thienyl)‐2,3,4,5‐tetraphenylsilole. J. Phys. Chem. B 109 (36), 17086–17093.

      66 66 Zhang, X.; Sørensen, J. K.; Fu, X.; Zhen, Y.; Zhao, G.; Jiang, L.; Dong, H.; Liu, J.; Shuai, Z.; Geng, H.; Bjørnholm, T.; Hu, W. (2014). Rubrene analogues with the aggregation‐induced emission enhancement behaviour. J. Mater. Chem. C 2 (5), 884–890.

      67 67 Yoshiharu, N.; Chitoshi, K.; Hiroyuki, K.; Takeshi, K. (2011). Diacenaphtho[1,2‐b;1′,2′‐d]silole and ‐pyrrole. Chem. Lett. 40 (12), 1437–1439.

      68 68 Katoh, R.; Suzuki, K.; Furube, A.; Kotani, M.; Tokumaru, K. (2009). Fluorescence quantum yield of aromatic hydrocarbon crystals. J. Phys. Chem. C 113 (7), 2961–2965.

      69 69 Varghese, S.; Park, S. K.; Casado, S.; Fischer, R. C.; Resel, R.; Milián‐Medina, B.; Wannemacher, R.; Park, S. Y.; Gierschner, J. (2013). Stimulated emission properties of sterically modified distyrylbenzene‐based H‐aggregate single crystals. J. Phys. Chem. Lett. 4 (10), 1597–1602.

      70 70 Zheng, X.; Peng, Q.; Zhu, L.; Xie, Y.; Huang, X.; Shuai, Z. (2016). Unraveling the aggregation effect on amorphous phase AIE luminogens: a computational study. Nanoscale 8, 15173–15180.

      71 71 Fan, X.; Sun, J.; Wang, F.; Chu, Z.; Wang, P.; Dong, Y.; Hu, R.; Tang, B. Z.; Zou, D. (2008). Photoluminescence and electroluminescence of hexaphenylsilole are enhanced by pressurization in the solid state. Chem. Commun. (26), 2989–2991.

      72 72 Gu, Y.; Wang, K.; Dai, Y.; Xiao, G.; Ma, Y.; Qiao, Y.; Zou, B. (2017). Pressure‐induced emission enhancement of carbazole: the restriction of intramolecular vibration. J. Phys. Chem. Lett. 8 (17), 4191–4196.

      73 73 Yuan, H.; Wang, K.; Yang, K.; Liu, B.; Zou, B. (2014). Luminescence properties of compressed tetraphenylethene: the role of intermolecular interactions. J. Phys. Chem. Lett. 5 (17), 2968–2973.

      74 74 Zhang, T.; Shi, W.; Wang, D.; Zhuo, S.; Peng, Q.; Shuai, Z. (2018). Pressure‐induced emission enhancement in hexaphenylsilole: a computational study. J. Mater. Chem. C 7, 1388–1398.

      75 75 Wang, D.; Su, H.; Kwok, R. T. K.;

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