[1] LI M, LIN W B, FANG L, et al. Recent progress on circularly polarized luminescence of chiral organic small molecules [J]. Acta Chimica Sinica,2017(75):1150-1163.
[2] ZINNA F, PASINI M, GALETTI F, et al. Design of lanthanide-based OLEDs with remarkable circularly polarized electroluminescence [J]. Adv Funct Mater,2017,27(1):1603719. doi: 10.1002/adfm.201603719
[3] SONG F, XU Z, ZHANG Q, et al. Highly efficient circularly polarized electroluminescence from aggregation-induced emission luminogens with amplified chirality and delayed fluorescence [J]. Adv Funct Mater,2018,28(17):1800051. doi: 10.1002/adfm.201800051
[4] YANG Y, DA COSTA R C, FUTHER M J, et al. Circularly polarized light detection by a chiral organic semiconductor transistor [J]. Nature Photonics,2013,7(8):634-638. doi: 10.1038/nphoton.2013.176
[5] TANG Z, IIDA H, HU H Y, et al. Remarkable enhancement of the enantioselectivity of an organocatalyzed asymmetric henry reaction assisted by helical poly(phenylacetylene)s bearing cinchona alkaloid pendants via an amide linkage [J]. ACS Macro Letters,2012,1(2):261-265. doi: 10.1021/mz200161s
[6] TAKAISHI K, IWACHIDO K, TAKEHANA R, et al. Evolving fluorophores into circularly polarized luminophores with a chiral naphthalene tetramer: Proposal of excimer chirality rule for circularly polarized luminescence [J]. J Am Chem Soc,2019,141(15):6185-6190. doi: 10.1021/jacs.9b02582
[7] KUMAR J, NAKASHIMA T, KAWAI T. Circularly polarized luminescence in chiral molecules and supramolecular assemblies [J]. J Phys Chem Lett,2015,6(17):3445-3452. doi: 10.1021/acs.jpclett.5b01452
[8] HAN T, ZU S, LI Z, et al. Reveal and control of chiral cathodoluminescence at subnanoscale [J]. Nano Lett,2018,18(1):567-572. doi: 10.1021/acs.nanolett.7b04705
[9] ZHANG L, WANG T Y, SHEN Z C, et al. Chiral nanoarchitectonics: Towards the design, self-assembly, and function of nanoscale chiral twists and helices [J]. Adv Mater,2016,28(6):1044-1059. doi: 10.1002/adma.201502590
[10] BOLES M A, ENGEL M, TALAPIN D V. Self-assembly of colloidal nanocrystals: From intricate structures to functional materials [J]. Chem Rev,2016,116(18):11220-11289. doi: 10.1021/acs.chemrev.6b00196
[11] LIU M H, OUYANG G H, NIU D, et al. Supramolecular gelatons: Towards the design of molecular gels [J]. Organic Chemistry Frontiers,2018,5(19):2885-2900. doi: 10.1039/C8QO00620B
[12] MIAO W, WANG S, LIU M H. Reversible quadruple switching with optical, chiroptical, helicity, and macropattern in self-assembled spiropyran gels [J]. Adv Funct Mater,2017,27(29):1701368. doi: 10.1002/adfm.201701368
[13] GOTO T, OKAZAKI Y, UEKI M, et al. Induction of strong and tunable circularly polarized luminescence of nonchiral, nonmetal, low-molecular-weight fluorophores using chiral nanotemplates [J]. Angew Chem Int Ed,2017,56(11):2989-2993. doi: 10.1002/anie.201612331
[14] WANG F, JI W, YANG P, et al. Inversion of circularly polarized luminescence of nanofibrous hydrogels through co-assembly with achiral coumarin derivatives [J]. ACS Nano,2019,13(6):7281-7290. doi: 10.1021/acsnano.9b03255
[15] JIANG H, JIANG Y, HAN J, et al. Helical nanostructures: Chirality transfer and a photodriven transformation from superhelix to nanokebab [J]. Angew Chem Int Ed,2019,131(3):795-800.
[16] YANG D, DUAN P, ZHANG L, et al. Chirality and energy transfer amplified circularly polarized luminescence in composite nanohelix [J]. Nat Commun,2017(8):15727.
[17] HAN J, DUAN P, LI X, et al. Amplification of circularly polarized luminescence through triplet-triplet annihilation-based photon upconversion [J]. J Am Chem Soc,2017,139(29):9783-9786. doi: 10.1021/jacs.7b04611
[18] YE Q, ZHU D D, XU LY, et al. Helical fibers with circularly polarized luminescence via ionic linkage and helically π-stacked assemblies of binaphthol and tetraphenylethylene derivatives [J]. J Mater Chem C,2016,4(7):1497-1503. doi: 10.1039/C5TC04174K
[19] HAN J, YOU J, LI X, et al. Full-color tunable circularly polarized luminescent nanoassemblies of achiral aIEgens in confined chiral nanotubes [J]. Adv Mater,2017,29(19):1606503. doi: 10.1002/adma.201606503
[20] HUO S, DUAN P, JIAO T, et al. Self-assembled luminescent quantum dots to generate full-color and white circularly polarized light [J]. Angew Chem Int Ed,2017,56(40):12174-12178. doi: 10.1002/anie.201706308
[21] SHI Y, DUAN P, HUO S, et al. Endowing perovskite nanocrystals with circularly polarized luminescence [J]. Adv Mater,2018,30(12):1705011. doi: 10.1002/adma.201705011
[22] JIN X, SANG Y, SHI Y, et al. Optically active upconverting nanoparticles with induced circularly polarized luminescence and enantioselectively triggered photopolymerization [J]. ACS Nano,2019,13(3):2804-2811. doi: 10.1021/acsnano.8b08273
[23] THANH-DINH N, HAMAD W Y, MACLACHLAN M J. Near-IR-sensitive upconverting nanostructured photonic cellulose films [J]. Adv Opt Mater,2017,5(1):1600514. doi: 10.1002/adom.201600514
[24] ZHAO T, HAN J, JIN X, et al. Enhanced circularly polarized luminescence from reorganized chiral emitters on the skeleton of a zeolitic imidazolate framework [J]. Angew Chem Int Ed,2019,58(15):4978-4982. doi: 10.1002/anie.201900052
[25] JIANG H, QU D, ZOU C, et al. Chiral nematic mesoporous silica films enabling multi-colour and on-off switchable circularly polarized luminescence [J]. New J Chem,2019,43(16):6111-6115. doi: 10.1039/C9NJ00724E
[26] ZHENG H Z, LI W R, LI W, et al. Uncovering the circular polarization potential of chiral photonic cellulose films for photonic applications [J]. Adv Mater,2018,30(13):1705948. doi: 10.1002/adma.201705948
[27] DI NUZZO D, KULKARNI C, ZHAO B, et al. High circular polarization of electroluminescence achieved via self-assembly of a light-emitting chiral conjugated polymer into multidomain cholesteric films [J]. ACS Nano,2017,11(12):12713-12722. doi: 10.1021/acsnano.7b07390
[28] ZOU C, QU D, JIANG H, et al. Bacterial cellulose: A versatile chiral host for circularly polarized luminescence [J]. Molecules,2019,24(6):1008. doi: 10.3390/molecules24061008
[29] MA J, WANG Y, LI X, et al. Aggregation-induced CPL response from chiral binaphthyl-based AIE-active polymers via supramolecular self-assembled helical nanowires [J]. Polymer,2018,143(9):184-189.
[30] ZHAO B, PAN K, DENG J. Intense circularly polarized luminescence contributed by helical chirality of monosubstituted polyacetylenes [J]. Macromolecules,2018,51(18):7104-7111. doi: 10.1021/acs.macromol.8b01545
[31] SAN JOSE B A, MATSUSHITA S, AKAJI K J. Lyotropic chiral nematic liquid crystalline aliphatic conjugated polymers based on disubstituted polyacetylene derivatives that exhibit high dissymmetry factors in circularly polarized luminescence [J]. J Am Chem Soc,2012,134(48):19795-19807. doi: 10.1021/ja3086565
[32] YAN J, OTA F, SAN JOSE B A, et al. Chiroptical resolution and thermal switching of chirality in conjugated polymer luminescence via selective reflection using a double-layered cell of chiral nematic liquid crystal [J]. Adv Funct Mater,2017,27(2):1604529. doi: 10.1002/adfm.201604529
[33] SAN JOSE B A, YAN J, AKAGI K. Dynamic switching of the circularly polarized luminescence of disubstituted polyacetylene by selective transmission through a thermotropic chiral nematic liquid crystal [J]. Angew Chem Int Ed,2014,53(40):10641-10644. doi: 10.1002/anie.201404250
[34] ZHAO B, PAN K, DENG J. Combining chiral helical polymer with achiral luminophores for generating full-color, on-off, and switchable circularly polarized luminescence [J]. Macromolecules,2018,52(1):376-384.
[35] WAN L, WADE J, SALERNO F, et al. Inverting the handedness of circularly polarized luminescence from light-emitting polymers using film thickness [J]. ACS Nano,2019,13(7):8099-8105. doi: 10.1021/acsnano.9b02940
[36] JIANG Q, XU X, YIN P A, et al. Circularly polarized luminescence of achiral ccyanine molecules assembled on DNA templates [J]. J Am Chem Soc,2019,141(24):9490-9494. doi: 10.1021/jacs.9b03305
[37] WANG H F, YANG K C, HSU W C, et al. Generalizing the effects of chirality on block copolymer assembly [J]. PNAS,2019,116(10):4080-4089. doi: 10.1073/pnas.1812356116
[38] LU X M, LI J M, ZHU D D, et al. Double-helical nanostructures with controllable handedness in bulk diblock copolymers [J]. Angew Chem Int Ed,2018,57(46):15148-15152. doi: 10.1002/anie.201809676