Handbook of Aggregation-Induced Emission, Volume 3

27 27 Xiong, J.‐B., Feng, H.‐T., Sun, J.‐P. et al. (2016). The fixed propeller‐like conformation of tetraphenylethlene that reveals aggregation‐induced emission effect, chiral recognition, and enhanced chiroptical property. J. Am. Chem. Soc. 13 (36): 11469–11472.

28 28 Qu, H., Wang, Y., Li, Z. et al. (2017). Molecular face‐rotating cube with emergent chiral and fluorescence properties. J. Am. Chem. Soc. 139 (50): 18142–18145.

29 29 Song, J., Wang, M., Zhou, X. et al. (2018). Unusual circularly polarized and aggregation‐induced near‐infrared phosphorescence of helical platinum(II) complexes with trtradentate salen ligands. Chem. Eur. J. 24 (28): 7128–7132.

30 30 Song, J., Wang, M., Xu, X. et al. (2019). 1D‐helical platinum(II) complexes bearing metal‐induced chirality, aggregation‐induced red phosphorescence, and circularly polarized luminescence. Dalton Trans. 48 (13): 4420–4428.

31 31 Shi, L., Zhu, L., Guo, J. et al. (2017). Self‐assembly of chiral gold clusters into crystalline nanocubes of exceptional optical activity. Angew. Chem. Int. Ed. 56 (48): 15397–15401.

32 32 Zhang, M.‐M., Dong, X.‐Y., Wang, Z.‐Y. et al. (2019). AIE triggers the circularly polarized luminescence of atomically precise enantiomeric copper(I) alkynyl clusters. Angew. Chem. Int. Ed. DOI: 10.1002/anie.201908909.

33 33 Kong, Y.‐J., Yan, Z.‐P., Li, S. et al. (2020). Photoresponsive properller‐like chiral AIE copper(I) clusters. Angew. Chem. Int. Ed. 59 (13): 5336–5340.

34 34 Liu, J., Su, H., Meng, L. et al. (2012). What makes efficient circularly polarised luminescence in the condensed phase: aggregation‐induced circular dichroism and light emission. Chem. Sci. 3 (9): 2737–2747.

35 35 Ng, J. C. Y., Liu, J., Su, H. et al. (2014). Complexation‐induced circular dichroism and circularly polarised luminescence of an aggregation‐induced emission luminogen. J. Mater. Chem. C 2 (1): 78–83.

36 36 Ng, J. C. Y., Li, H., Yuan, Q. et al. (2014). Valine‐containing silole: synthesis, aggregation‐ induced chirality, luminescence enhancement chiral‐polarized luminescence and self‐assembled structures. J. Mater. Chem. C 2 (23): 4615–4621.

37 37 Li, H., Xue, S., Su, H. et al. (2016). Click synthesis, aggregation‐induced emission and chirality, circularly polarized luminescence, and helical self‐assembly of a leucine‐containing silole. Small 12 (47): 6593–6601.

38 38 Xue, S., Meng, L., Wen, R. et al. (2017). unexpected aggreation induced circular dichroism, circular polarized luminescence and helical assembly from achiral hexaphenylsilole (HPS). RSC Adv. 7 (40): 24841–24847.

39 39 Li, H., Cheng, J., Zhao, Y. et al. (2014). L‐valine methyl ester‐containing tetraphenylethene: aggregation‐induced emission, aggregation‐induced circular dichiroism, circularly polarized luminescence, and helical self‐assembly. Mater. Horiz. 1 (5): 518–521.

40 40 Li, H., Cheng, J., Deng, H. et al. (2015). Aggregation‐induced chirality, circularly polarized luminescence, and helical self‐assembly of a leucine‐containing AIE luminogen. J. Mater. Chem. C 3 (10): 2399–2404.

41 41 Li, H., Zheng, X., Su, H. et al. (2016). Synthesis, optical properties, and helical self‐assembly of a bivaline‐containing tetraphenylethene. Sci. Rep. 6: 19277.

42 42 Li, H., Yuan, W., He, H. et al. (2017). Circularly polarized luminescence and controllable helical self‐assembly of an aggregation‐induced emission luminogen. Dyes Pigm. 138: 129–134.

43 43 Zhang, S., Fan, J., Wang, Y. et al. (2019). Tunable aggregation‐induced circularly polarized luminescecne of chiral AIEgens via the regulation of mono/di‐substituents of molecules or nanostructures of self‐assemblies. Mater. Chem. Front. 3 (10): 2066–2071.

44 44 Qiao, W.‐G., Xiong, J.‐B., Yuan, Y.‐X. et al. (2018). Chiroptical property of TPE triangular macrocycle crown ethers from propeller‐like chirality induced by chiral acid. J. Mater. Chem. C 6 (13): 3427–3434.

45 45 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. J. Mater. Chem. C 7 (27): 8236–8243.

46 46 Huang, G., Wen, R., Wang, Z. et al. (2018). Novel chiral aggregation induced emission molecules: self‐assembly, circularly polarized luminescence and copper(II) ion detection. Mater. Chem. Front. 2 (10): 1884–1992.

47 47 Shang, H., Ding, Z., Shen, Y. et al. (2020). Multi‐color tunable circularly polarized luminescence in one single AIE system. Chem. Sci. 11 (8): 2169–2174.

48 48 Ikeda, T., Takayama, M., Kumar, J. et al. (2015). Novel helical assembly of a Pt(II) phenylbipyridine complex directed by metal‐metal interaction and aggregation‐induced circularly polarized emission. Dalton Trans. 44 (29): 13156–13162.

49 49 Jiang, Q., Xu, X., Yin, P.‐A. et al. (2019). Circularly polarized luminescence of achiral cyanine molecules assembled on DNA templates. J. Am. Chem. Soc. 141 (24): 9490–9494.

50 50 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. Org. Lett. 22 (5): 1836–1840.

51 51 Han, J., You, J., Li, X. et al. (2017). Full‐color tunable circularly polarized luminescent nano‐assembles of achiral AIEgens in confined chiral nanotubes. Adv. Mater. 29 (19): 1606503.

52 52 Li, P., Lü, B., Han, D. et al. (2019). Stoichiometry‐controlled inversion of circularly polarized luminescence in co‐assembly of chiral gelators with an achiral tetraphenylethylene derivative. Chem. Commun. 55 (15): 2194–2197.

53 53 Hu, L., Li, K., Shang, W. et al. (2020). Emerging cubic chirality in γCD‐MOF for fabricating circularly polarized luminescent crystalline materials and the size effect. Angew. Chem. Int. Ed. 59 (12): 4953–4958.

54 54Khorloo, M., Cheng, Y., Zhang, H. et al. (2020). Polymorph selectivity of an AIE luminogen under nano‐confinement to visualize polymer microstructures. Chem. Sci. 11 (4): 997–1005.

55 55 Zhang, J., Liu, Q., Wu, W. et al. (2019). Real‐time montoring of hierarchical self‐assembly and induction of circularly polarized luminescence from achiral luminogens. ACS Nano 13 (3): 3618–3628.

56 56 Zhang, W., Chang, H., Ai, J. et al. (2019). Spontaneous chiral self‐assembly of achiral AIEgens into AIEgen‐silica hybrid nanotubes. Chem. Commun. 55 (96): 14438–14441.

57 57 Liu, X., Jiao, J., Jiang, X. et al. (2013). A tetraphenylethene‐based chiral polymer: an AIE luminogen with high and tunable CPL dissymmetry factor. J. Mater. Chem. C 1 (31): 4713–4719.

58 58 Zhang, S., Sheng, Y., Wei, G. et al. (2015). Aggregation‐induced circularly polarized luminescence of an (R)‐binaphthyl‐based AIE‐active chiral conjugated polymer with self‐assembled helical nanofibers. Polym. Chem. 6 (13): 2416–2422.

59 59 Ma, J., Wang, Y., Li, X. et al. (2018). Aggregation‐induced CPL response from chiral binaphthyl‐based AIE‐active polymers via supramolecular self‐assembled helical nanowires. Polymer 143: 184–189.

60 60 Yang, L., Zhang, Y., Zhang, X. et al. (2018). Doping‐free circularly polarized electroluminescence of AIE‐active chiral binaphthyl‐based polymers. Chem. Commun. 54 (69): 9663–9666.

61 61 Wang, Z., Liu, S., Wang, Y. et al. (2017). Tunable AICPL of (S)‐binaphthyl‐based three‐component polymers via FRET mechanism. Macromol. Rapid Commun. 38 (14): 1700150.

62 62 Wang, Z., Fang, Y., Tao, X. et al. (2017). Deep red aggregation‐induced CPL emission behavior of four‐component tunable AIE‐active chiral polymers via two FRET pairs mechanism. Polymer 130: 61–67.

63 63 Zhang, C., Li, M., Lu, H.‐Y. et al. (2018). Synthesis, chiroptical properties, and self‐assembled nanoparticles of chiral conjugated polymers based on optically stable helical aromatic esters. RSC Adv. 8 (2): 1014–1021.