Prlj, A., Došlić, N., and Corminboeuf, C. (2016). How does tetraphenylethylene relax from its excited states? Physical Chemistry Chemical Physics 18 (17): 11606–11609.56 56 Gao, Y.‐J., Chang, X.‐P., Liu, X.‐Y. et al. (2017). Excited‐state decay paths in tetraphenylethene derivatives. The Journal of Physical Chemistry A 121 (13): 2572–2579.
57 57 Cai, Y., Du, L., Samedov, K. et al. (2018). Deciphering the working mechanism of aggregation‐induced emission of tetraphenylethylene derivatives by ultrafast spectroscopy. Chemical Science 9 (20): 4662–4670.
58 58 Kokado, K., Machida, T., Iwasa, T. et al. (2018). Twist of C=C bond plays a crucial role in the quenching of AIE‐active tetraphenylethene derivatives in solution. The Journal of Physical Chemistry C 122 (1): 245–251.
59 59 Tasso, T. T., Furuyama, T., and Kobayashi, N. (2015). Dinitriles bearing AIE‐active moieties: synthesis, E/Z isomerization, and fluorescence properties. Chemistry–A European Journal 21 (12): 4817–4824.
60 60 Chung, J. W., Yoon, S. J., An, B. K. et al. (2013). High‐contrast on/off fluorescence switching via reversible E–Z isomerization of diphenylstilbene containing the α‐cyanostilbenic moiety. The Journal of Physical Chemistry C 117 (21): 11285–11291.
61 61 Yamamoto, N. (2018). Mechanisms of aggregation‐induced emission and photo/thermal E/Z isomerization of a cyanostilbene derivative: theoretical insights. The Journal of Physical Chemistry C 122 (23): 12434–12440.
62 62 Duan, P., Yanai, N., Kurashige, Y. et al. (2015). Aggregation‐induced photon upconversion through control of the triplet energy landscapes of the solution and solid states. Angewandte Chemie International Edition 54 (26): 7544–7549.
63 63 Shi, J., Aguilar Suarez, L. E., Yoon, S. J. et al. (2017). Solid state luminescence enhancement in π‐conjugated materials: unraveling the mechanism beyond the framework of AIE/AIEE. The Journal of Physical Chemistry C 121 (41): 23166–23183.
64 64 Tong, H., Dong, Y., Hong, Y. et al. (2007). Aggregation‐induced emission: effects of molecular structure, solid‐state conformation, and morphological packing arrangement on light‐emitting behaviors of diphenyldibenzofulvene derivatives. The Journal of Physical Chemistry C 111 (5): 2287–2294.
65 65 Gao, X., Peng, Q., Niu, Y. et al. (2012). Theoretical insight into the aggregation induced emission phenomena of diphenyldibenzofulvene: a nonadiabatic molecular dynamics study. Physical Chemistry Chemical Physics 14 (41): 14207–14216.
66 66 Li, Q. and Blancafort, L. (2013). A conical intersection model to explain aggregation induced emission in diphenyl dibenzofulvene. Chemical Communications 49 (53): 5966–5968.
67 67 Ruiz‐Barragan, S., Morokuma, K., and Blancafort, L. (2015). Conical intersection optimization using composed steps inside the ONIOM (QM: MM) scheme: CASSCF: UFF implementation with microiterations. Journal of Chemical Theory and Computation 11 (4): 1585–1594.
68 68 Wang, B., Wang, X., Wang, W. et al. (2016). Exploring the mechanism of fluorescence quenching and aggregation‐induced emission of a phenylethylene derivative by QM (CASSCF and TDDFT) and ONIOM (QM: MM) calculations. The Journal of Physical Chemistry C 120 (38): 21850–21857.
69 69 Jiang, M., He, Z., Zhang, Y. et al. (2017). Development of benzylidene‐methyloxazolone based AIEgens and decipherment of their working mechanism. Journal of Materials Chemistry C 5 (29): 7191–7199.
Конец ознакомительного фрагмента.
Текст предоставлен ООО «ЛитРес».
Прочитайте эту книгу целиком, купив полную легальную версию на ЛитРес.
Безопасно оплатить книгу можно банковской картой Visa, MasterCard, Maestro, со счета мобильного телефона, с платежного терминала, в салоне МТС или Связной, через PayPal, WebMoney, Яндекс.Деньги, QIWI Кошелек, бонусными картами или другим удобным Вам способом.
