Circularly polarized luminescence in molecular recognition systems: Recent achievements
Circularly polarized luminescence (CPL) dyes are recognized to be new generation materials and have been actively developed. Molecular recognition systems provide nice approaches to novel CPL materials, such as stimuli‐responsive switches and chemical sensing materials. CPL may be induced simply by...
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Published in | Chirality (New York, N.Y.) Vol. 35; no. 2; pp. 92 - 103 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
United States
Wiley Subscription Services, Inc
01.02.2023
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Online Access | Get full text |
ISSN | 0899-0042 1520-636X 1520-636X |
DOI | 10.1002/chir.23522 |
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Abstract | Circularly polarized luminescence (CPL) dyes are recognized to be new generation materials and have been actively developed. Molecular recognition systems provide nice approaches to novel CPL materials, such as stimuli‐responsive switches and chemical sensing materials. CPL may be induced simply by mixing chiral or achiral, luminescent or nonluminescent host and guest; there are several combinations. Molecular recognition can potentially save time and effort to construct well‐ordered chiral structures with noncovalent attractive interactions as compared with the multi‐step synthesis of covalently bonded dyes. It is a challenging subject to engage molecular recognition events with CPL, and it is important and interesting to see how it is achieved. In fact, simple molecular recognition systems can even enable the fine adjustment of CPL performance and detailed conformational/configurational analysis of the excited state. Here we overview the recent achievements of simple host–guest complexes capable of exhibiting CPL, summarizing concisely the host/guest structures, CPL intensities, and characteristics.
In this review, simple host–guest systems capable of exhibiting circularly polarized luminescence (CPL) are overviewed. The pioneering works summarized herein will provide some hints on the creation of easy‐to‐prepare and high‐performance CPL materials in future. |
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AbstractList | Circularly polarized luminescence (CPL) dyes are recognized to be new generation materials and have been actively developed. Molecular recognition systems provide nice approaches to novel CPL materials, such as stimuli‐responsive switches and chemical sensing materials. CPL may be induced simply by mixing chiral or achiral, luminescent or nonluminescent host and guest; there are several combinations. Molecular recognition can potentially save time and effort to construct well‐ordered chiral structures with noncovalent attractive interactions as compared with the multi‐step synthesis of covalently bonded dyes. It is a challenging subject to engage molecular recognition events with CPL, and it is important and interesting to see how it is achieved. In fact, simple molecular recognition systems can even enable the fine adjustment of CPL performance and detailed conformational/configurational analysis of the excited state. Here we overview the recent achievements of simple host–guest complexes capable of exhibiting CPL, summarizing concisely the host/guest structures, CPL intensities, and characteristics. Circularly polarized luminescence (CPL) dyes are recognized to be new generation materials and have been actively developed. Molecular recognition systems provide nice approaches to novel CPL materials, such as stimuli-responsive switches and chemical sensing materials. CPL may be induced simply by mixing chiral or achiral, luminescent or nonluminescent host and guest; there are several combinations. Molecular recognition can potentially save time and effort to construct well-ordered chiral structures with noncovalent attractive interactions as compared with the multi-step synthesis of covalently bonded dyes. It is a challenging subject to engage molecular recognition events with CPL, and it is important and interesting to see how it is achieved. In fact, simple molecular recognition systems can even enable the fine adjustment of CPL performance and detailed conformational/configurational analysis of the excited state. Here we overview the recent achievements of simple host-guest complexes capable of exhibiting CPL, summarizing concisely the host/guest structures, CPL intensities, and characteristics.Circularly polarized luminescence (CPL) dyes are recognized to be new generation materials and have been actively developed. Molecular recognition systems provide nice approaches to novel CPL materials, such as stimuli-responsive switches and chemical sensing materials. CPL may be induced simply by mixing chiral or achiral, luminescent or nonluminescent host and guest; there are several combinations. Molecular recognition can potentially save time and effort to construct well-ordered chiral structures with noncovalent attractive interactions as compared with the multi-step synthesis of covalently bonded dyes. It is a challenging subject to engage molecular recognition events with CPL, and it is important and interesting to see how it is achieved. In fact, simple molecular recognition systems can even enable the fine adjustment of CPL performance and detailed conformational/configurational analysis of the excited state. Here we overview the recent achievements of simple host-guest complexes capable of exhibiting CPL, summarizing concisely the host/guest structures, CPL intensities, and characteristics. Circularly polarized luminescence (CPL) dyes are recognized to be new generation materials and have been actively developed. Molecular recognition systems provide nice approaches to novel CPL materials, such as stimuli-responsive switches and chemical sensing materials. CPL may be induced simply by mixing chiral or achiral, luminescent or nonluminescent host and guest; there are several combinations. Molecular recognition can potentially save time and effort to construct well-ordered chiral structures with noncovalent attractive interactions as compared with the multi-step synthesis of covalently bonded dyes. It is a challenging subject to engage molecular recognition events with CPL, and it is important and interesting to see how it is achieved. In fact, simple molecular recognition systems can even enable the fine adjustment of CPL performance and detailed conformational/configurational analysis of the excited state. Here we overview the recent achievements of simple host-guest complexes capable of exhibiting CPL, summarizing concisely the host/guest structures, CPL intensities, and characteristics. Circularly polarized luminescence (CPL) dyes are recognized to be new generation materials and have been actively developed. Molecular recognition systems provide nice approaches to novel CPL materials, such as stimuli‐responsive switches and chemical sensing materials. CPL may be induced simply by mixing chiral or achiral, luminescent or nonluminescent host and guest; there are several combinations. Molecular recognition can potentially save time and effort to construct well‐ordered chiral structures with noncovalent attractive interactions as compared with the multi‐step synthesis of covalently bonded dyes. It is a challenging subject to engage molecular recognition events with CPL, and it is important and interesting to see how it is achieved. In fact, simple molecular recognition systems can even enable the fine adjustment of CPL performance and detailed conformational/configurational analysis of the excited state. Here we overview the recent achievements of simple host–guest complexes capable of exhibiting CPL, summarizing concisely the host/guest structures, CPL intensities, and characteristics. In this review, simple host–guest systems capable of exhibiting circularly polarized luminescence (CPL) are overviewed. The pioneering works summarized herein will provide some hints on the creation of easy‐to‐prepare and high‐performance CPL materials in future. |
Author | Maeda, Chihiro Takaishi, Kazuto Ema, Tadashi |
Author_xml | – sequence: 1 givenname: Kazuto orcidid: 0000-0003-4979-7375 surname: Takaishi fullname: Takaishi, Kazuto email: takaishi@okayama-u.ac.jp organization: Okayama University – sequence: 2 givenname: Chihiro orcidid: 0000-0003-4370-3905 surname: Maeda fullname: Maeda, Chihiro organization: Okayama University – sequence: 3 givenname: Tadashi orcidid: 0000-0002-2160-6840 surname: Ema fullname: Ema, Tadashi email: ema@cc.okayama-u.ac.jp organization: Okayama University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36477924$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1021/jacs.9b02582 10.1016/j.ccr.2021.214329 10.1007/978‐981‐15‐2309‐0 10.3390/molecules23123376 10.1007/978‐981‐15‐5085‐0_16 10.1021/acs.jpclett.5b01452 10.1016/j.ccr.2022.214640 10.1002/chem.201903252 10.1016/j.ccr.2019.06.017 10.1002/adma.202003615 10.1021/ja00209a033 10.1039/D1SC04403F 10.1021/acs.chemrev.0c00195 10.1002/anie.202209340 10.1063/1.3582917 10.1021/jacs.8b01860 10.1002/anie.202205725 10.1021/jacs.0c05369 10.1021/acs.jpclett.1c02013 10.1021/cr60310a001 10.1016/j.ccr.2020.213329 10.1039/D1CC05902E 10.1039/C6SC01808D 10.1002/adma.202005760 10.1021/acs.chemrev.8b00770 10.1039/D0SC01011A 10.1021/jacs.9b07143 10.1039/D0CS00191K 10.1002/smll.201601455 10.1007/s11426‐021‐1146‐6 10.1002/anie.201800198 10.1002/chem.202002791 10.1021/acs.chemrev.0c01017 10.1021/ic500196m 10.1039/C5CC08488A 10.1039/D1SC02335G 10.1002/anie.201408193 10.1039/D1SC02305E 10.1021/cr400477t 10.1021/ja00307a055 10.1002/anie.202108209 10.1002/cptc.202100228 10.1021/jacs.9b13184 10.1002/anie.202200727 10.1039/B909430J 10.1002/anie.202105593 10.1002/adma.202008785 10.1021/jacs.0c07707 10.1002/chir.22382 10.1039/C9CC01138B 10.1002/cptc.202100162 10.1016/j.chempr.2021.07.017 10.1002/adom.201800538 10.1016/j.jphotochemrev.2022.100500 10.1039/C9TC07022B 10.1002/tcr.202100199 10.1021/acs.joc.8b00162 10.1002/cptc.202100124 10.3389/fchem.2020.00448 10.1016/j.mtchem.2021.100651 10.1002/cptc.202100256 10.1002/chem.201501178 10.1016/0009‐2614(81)80311‐9 10.1002/adma.201900110 10.1002/advs.202000804 10.1002/chem.201803215 10.1021/acs.chemrev.6b00354 10.1002/asia.201801777 10.1002/cptc.201800015 10.1016/j.chempr.2019.08.006 10.1002/asia.201600798 10.1021/acsami.9b20568 10.1021/ic202355s 10.1021/acsomega.9b03613 10.1002/chir.22647 10.31635/ccschem.020.202000509 10.1021/cr00071a001 10.1016/j.tetlet.2019.151232 10.1021/jacsau.1c00084 10.1039/C8SC02935K 10.1039/C9CC06861A 10.1002/cptc.202100154 10.1002/slct.201800213 10.1039/C6DT01212D 10.1016/j.xcrp.2021.100692 10.1351/PAC‐CON‐12‐11‐09 10.3389/fchem.2020.00458 10.1039/C6OB00752J 10.1039/C9CS00680J 10.1007/s10847‐021‐01108‐z 10.1039/C8CC09114E 10.1039/C2CS35242G 10.1039/C6CC01277A |
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References | 2022; 453 2021; 27 2021; 64 2020; 120 2019; 55 2019; 14 2022; 23 2011; 98 2020; 12 2020; 11 2018; 83 2022; 22 2021; 121 1981; 83 2012; 51 2020; 8 2018; 6 2020; 7 2018; 9 2020; 5 2019; 60 2018; 3 2018; 2 2020; 2 2021; 33 1986; 86 2019; 25 2020; 49 1977; 77 2019; 119 2016; 116 2019; 397 2020; 416 2016; 45 2014; 53 2021; 7 2015; 6 2021; 5 2018; 140 2019; 5 2022; 50 2020; 142 2013; 85 2009 2016; 52 1985; 107 2020; 32 2018; 23 2021; 1 2019; 141 2014; 114 2016; 14 2016; 12 2018; 24 2016; 11 2021; 57 2016; 7 2015; 27 2021; 12 2022; 3 2022; 61 2022; 6 2020 2015; 21 2022; 13 1988; 110 2016; 28 2021; 60 2022; 468 2012; 41 2022; 102 2018; 57 e_1_2_5_27_1 e_1_2_5_25_1 e_1_2_5_48_1 e_1_2_5_23_1 e_1_2_5_46_1 e_1_2_5_21_1 e_1_2_5_44_1 e_1_2_5_65_1 e_1_2_5_88_1 e_1_2_5_67_1 e_1_2_5_69_1 e_1_2_5_29_1 e_1_2_5_80_1 e_1_2_5_82_1 e_1_2_5_61_1 e_1_2_5_84_1 e_1_2_5_63_1 e_1_2_5_86_1 e_1_2_5_42_1 e_1_2_5_40_1 e_1_2_5_15_1 e_1_2_5_38_1 e_1_2_5_17_1 e_1_2_5_36_1 e_1_2_5_59_1 e_1_2_5_9_1 e_1_2_5_11_1 e_1_2_5_34_1 e_1_2_5_57_1 e_1_2_5_7_1 e_1_2_5_13_1 e_1_2_5_32_1 e_1_2_5_55_1 e_1_2_5_5_1 e_1_2_5_76_1 e_1_2_5_3_1 e_1_2_5_78_1 e_1_2_5_19_1 e_1_2_5_91_1 e_1_2_5_70_1 e_1_2_5_93_1 e_1_2_5_72_1 e_1_2_5_74_1 e_1_2_5_30_1 e_1_2_5_53_1 e_1_2_5_51_1 e_1_2_5_28_1 e_1_2_5_49_1 e_1_2_5_26_1 e_1_2_5_47_1 e_1_2_5_24_1 e_1_2_5_45_1 e_1_2_5_22_1 e_1_2_5_43_1 e_1_2_5_66_1 e_1_2_5_87_1 e_1_2_5_68_1 e_1_2_5_89_1 e_1_2_5_81_1 e_1_2_5_60_1 e_1_2_5_83_1 e_1_2_5_62_1 e_1_2_5_64_1 e_1_2_5_85_1 e_1_2_5_20_1 e_1_2_5_41_1 e_1_2_5_14_1 e_1_2_5_39_1 e_1_2_5_16_1 e_1_2_5_37_1 e_1_2_5_58_1 e_1_2_5_8_1 e_1_2_5_10_1 e_1_2_5_35_1 e_1_2_5_56_1 e_1_2_5_6_1 e_1_2_5_12_1 e_1_2_5_33_1 e_1_2_5_54_1 e_1_2_5_4_1 e_1_2_5_77_1 e_1_2_5_2_1 e_1_2_5_79_1 e_1_2_5_18_1 e_1_2_5_90_1 e_1_2_5_71_1 e_1_2_5_92_1 e_1_2_5_73_1 e_1_2_5_94_1 e_1_2_5_75_1 e_1_2_5_31_1 e_1_2_5_52_1 e_1_2_5_50_1 |
References_xml | – volume: 468 year: 2022 article-title: Metal‐organic materials with circularly polarized luminescence publication-title: Coord Chem Rev – volume: 83 start-page: 161 issue: 1 year: 1981 end-page: 164 article-title: Excited‐state optical activity of a cyclodextrin inclusion compound publication-title: Chem Phys Lett – volume: 55 start-page: 4095 issue: 28 year: 2019 end-page: 4098 article-title: Off–off–on chiroptical property switching of a pyrene luminophore by stepwise helicate formation publication-title: Chem Commun – volume: 41 start-page: 7673 issue: 23 year: 2012 end-page: 7686 article-title: Lanthanide complexes as chiral probes exploiting circularly polarized luminescence publication-title: Chem Soc Rev – volume: 61 issue: 35 year: 2022 article-title: Guest‐modulated circularly polarized luminescence by ligand‐to‐ligand chirality transfer in heteroleptic Pd coordination cages publication-title: Angew Chem Int Ed – volume: 102 start-page: 133 issue: 1‐2 year: 2022 end-page: 142 article-title: Circularly polarized luminescence (CPL) characteristics of hydrophobic pyrene derivatives/γ‐cyclodextrin (γ‐CD) complexes in aqueous solution dissolved by grinding publication-title: J Incl Phenom Macrocycl Chem – volume: 60 start-page: 21927 issue: 40 year: 2021 end-page: 21933 article-title: Saucer[ ]arenes: synthesis, structure, complexation, and guest‐induced circularly polarized luminescence property publication-title: Angew Chem Int Ed – volume: 6 issue: 3 year: 2022 article-title: Recent progress in circularly polarized luminescence of [2.2]paracyclophane derivatives publication-title: ChemPhotoChem – volume: 397 start-page: 76 year: 2019 end-page: 90 article-title: Lanthanides complexes – chiral sensing of biomolecules publication-title: Coord Chem Rev – volume: 2 start-page: 2749 issue: 11 year: 2020 end-page: 2763 article-title: Adaptive chirality of an achiral cage: chirality transfer, induction, and circularly polarized luminescence through aqueous host–guest complexation publication-title: CCS Chem – volume: 23 year: 2022 article-title: Circularly polarized luminescence based on small organic fluorophores publication-title: Mater Today Chem – volume: 57 start-page: 2889 issue: 11 year: 2018 end-page: 2893 article-title: Stable enantiomers displaying thermally activated delayed fluorescence: efficient OLEDs with circularly polarized electroluminescence publication-title: Angew Chem Int Ed – volume: 49 start-page: 9095 issue: 24 year: 2020 end-page: 9120 article-title: Supramolecular chiroptical switches publication-title: Chem Soc Rev – volume: 5 start-page: 3786 issue: 8 year: 2020 end-page: 3791 article-title: Steric and electronic control of chiral Eu(III) complexes for effective circularly polarized luminescence publication-title: ACS Omega – volume: 119 start-page: 8435 issue: 14 year: 2019 end-page: 8478 article-title: Main‐group‐based electro‐ and photoactive chiral materials publication-title: Chem Rev – volume: 7 start-page: 5663 issue: 9 year: 2016 end-page: 5670 article-title: Stapled helical ‐OPE foldamers as new circularly polarized luminescence emitters based on carbophilic interactions with Ag(I)‐sensitivity publication-title: Chem Sci – volume: 6 start-page: 3445 issue: 17 year: 2015 end-page: 3452 article-title: Circularly polarized luminescence in chiral molecules and supramolecular assemblies publication-title: J Phys Chem Lett – volume: 140 start-page: 5334 issue: 16 year: 2018 end-page: 5338 article-title: Binaphthyl−bipyridyl cyclic dyads as a chiroptical switch publication-title: J Am Chem Soc – volume: 53 start-page: 14392 issue: 52 year: 2014 end-page: 14396 article-title: A doubly alkynylpyrene‐threaded [4]rotaxane that exhibits strong circularly polarized luminescence from the spatially restricted excimer publication-title: Angew Chem Int Ed – volume: 98 issue: 16 year: 2011 article-title: Optical communication of spin information between light emitting diodes publication-title: Appl Phys Lett – volume: 61 issue: 19 year: 2022 article-title: ATP‐induced emergent circularly polarized luminescence and encryption publication-title: Angew Chem Int Ed – volume: 33 issue: 26 year: 2021 article-title: Recent progress of chiral perovskites: materials, synthesis, and properties publication-title: Adv Mater – volume: 5 start-page: 3058 issue: 12 year: 2019 end-page: 3095 article-title: Chirality and chiroptics of lanthanide molecular and supramolecular assemblies publication-title: Chem – volume: 45 start-page: 8355 issue: 20 year: 2016 end-page: 8366 article-title: Induced europium CPL for the selective signalling of phosphorylated amino‐acids and ‐phosphorylated hexapeptides publication-title: Dalton Trans – volume: 142 start-page: 1774 issue: 4 year: 2020 end-page: 1779 article-title: Solvent‐induced sign inversion of circularly polarized luminescence: control of excimer chirality by hydrogen bonding publication-title: J Am Chem Soc – volume: 121 start-page: 2373 issue: 4 year: 2021 end-page: 2412 article-title: Chiroptical properties of symmetric double, triple, and multiple helicenes publication-title: Chem Rev – volume: 12 start-page: 14570 issue: 43 year: 2021 end-page: 14576 article-title: Chiral exciplex dyes showing circularly polarized luminescence: extension of the excimer chirality rule publication-title: Chem Sci – volume: 6 issue: 17 year: 2018 article-title: Recent progress on circularly polarized luminescent materials for organic optoelectronic devices publication-title: Adv Optical Mater – volume: 83 start-page: 4455 issue: 8 year: 2018 end-page: 4463 article-title: Pyrene‐containing ‐oligo(phenylene)ethynylene foldamer as a ratiometric probe based on circularly polarized luminescence publication-title: J Org Chem – volume: 33 issue: 12 year: 2021 article-title: Polarization‐sensitive halide perovskites for polarized luminescence and detection: recent advances and perspectives publication-title: Adv Mater – volume: 2 start-page: 386 issue: 5 year: 2018 end-page: 402 article-title: Circularly polarized luminescence and circular dichroisms in small organic molecules: correlation between excitation and emission dissymmetry factors publication-title: ChemPhotoChem – volume: 7 start-page: 2771 issue: 10 year: 2021 end-page: 2786 article-title: Endohedral functionalization of chiral metal‐organic cages for encapsulating achiral dyes to induce circularly polarized luminescence publication-title: Chem – volume: 14 start-page: 561 issue: 4 year: 2019 end-page: 567 article-title: Chiral sensing using circularly polarized luminescence of bis(phenanthroline dicarboxylic acid) Eu complex induced by allosteric‐type interaction with amino acid molecules publication-title: Chem Asian J – volume: 6 issue: 1 year: 2022 article-title: Circular polarization of luminescence as a tool to study molecular dynamical processes publication-title: ChemPhotoChem – volume: 107 start-page: 6117 issue: 21 year: 1985 end-page: 6118 article-title: Chiral pyrene excimer in the γ‐cyclodextrin cavity publication-title: J Am Chem Soc – volume: 32 issue: 41 year: 2020 article-title: Circularly polarized luminescence in nanoassemblies: generation, amplification, and application publication-title: Adv Mater – volume: 12 start-page: 9520 issue: 8 year: 2020 end-page: 9527 article-title: Rational design of axially chiral platinabinaphthalenes with aggregation‐induced emission for red circularly polarized phosphorescent organic light‐emitting diodes publication-title: ACS Appl Mater Interfaces – volume: 52 start-page: 5171 issue: 29 year: 2016 end-page: 5174 article-title: Photoswitching of an intramolecular chiral stack in a helical tetrathiazole publication-title: Chem Commun – volume: 9 start-page: 7043 issue: 35 year: 2018 end-page: 7052 article-title: Combined reversible switching of ECD and quenching of CPL with chiral fluorescent macrocycles publication-title: Chem Sci – volume: 12 start-page: 6495 issue: 47 year: 2016 end-page: 6512 article-title: Circularly‐polarized luminescence (CPL) from chiral AIE molecules and macrostructures publication-title: Small – volume: 6 issue: 3 year: 2022 article-title: Tunable circularly polarized luminescent supramolecular systems: approaches and applications publication-title: ChemPhotoChem – volume: 22 issue: 1 year: 2022 article-title: Chiral triarylborane‐based small organic molecules for circularly polarized luminescence publication-title: Chem Rec – volume: 110 start-page: 204 issue: 1 year: 1988 end-page: 209 article-title: Binding sites of pyrene and related compounds and chiral excimer formation in the cavities of cyclodextrins and branched cyclodextrins publication-title: J Am Chem Soc – volume: 33 issue: 47 year: 2021 article-title: Chiral perovskites for next‐generation photonics: from chirality transfer to chiroptical activity publication-title: Adv Mater – volume: 27 start-page: 1 issue: 1 year: 2015 end-page: 13 article-title: Lanthanide circularly polarized luminescence: bases and applications publication-title: Chirality – volume: 141 start-page: 6185 issue: 15 year: 2019 end-page: 6190 article-title: Evolving fluorophores into circularly polarized luminophores with a chiral naphthalene tetramer: proposal of excimer chirality rule for circularly polarized luminescence publication-title: J Am Chem Soc – volume: 53 start-page: 5527 issue: 11 year: 2014 end-page: 5537 article-title: Specific chiral sensing of amino acids using induced circularly polarized luminescence of bis(diimine)dicarboxylic acid europium(III) complexes publication-title: Inorg Chem – volume: 60 issue: 46 year: 2019 article-title: Circularly polarized luminescence from pyrene excimers publication-title: Tetrahedron Lett – volume: 57 start-page: 13554 issue: 99 year: 2021 end-page: 13557 article-title: Chiral macrocycle‐induced circularly polarized luminescence of a twisted intramolecular charge transfer dye publication-title: Chem Commun – volume: 3 start-page: 3576 issue: 13 year: 2018 end-page: 3581 article-title: Synthesis, optical resolution, and circularly polarized luminescence of an axially chiral porphyrin dimer publication-title: ChemistrySelect – volume: 23 issue: 12 year: 2018 article-title: Recent theoretical and experimental progress in circularly polarized luminescence of small organic molecules publication-title: Molecules – volume: 21 start-page: 13488 issue: 39 year: 2015 end-page: 13500 article-title: Circularly polarized luminescence from simple organic molecules publication-title: Chem Eur J – volume: 8 year: 2020 article-title: The progress and perspective of organic molecules with switchable circularly polarized luminescence publication-title: Front Chem – volume: 86 start-page: 1 issue: 1 year: 1986 end-page: 16 article-title: Circularly polarized luminescence spectroscopy publication-title: Chem Rev – volume: 52 start-page: 2481 issue: 12 year: 2016 end-page: 2484 article-title: Oligoamylose‐entwined porphyrin: excited‐state induced‐fit for chirality induction publication-title: Chem Commun – volume: 28 start-page: 696 issue: 10 year: 2016 end-page: 707 article-title: Circularly polarized luminescence: a review of experimental and theoretical aspects publication-title: Chirality – volume: 8 year: 2020 article-title: Irreverent nature of dissymmetry factor and quantum yield in circularly polarized luminescence of small organic molecules publication-title: Front Chem – volume: 14 start-page: 4590 issue: 20 year: 2016 end-page: 4594 article-title: Zwitterionic [4]helicene: a water‐soluble and reversible pH‐triggered ECD/CPL chiroptical switch in the UV and red spectral regions publication-title: Org Biomol Chem – volume: 416 year: 2020 article-title: Chiral AIEgens–chiral recognition, CPL materials and other chiral applications publication-title: Coord Chem Rev – volume: 25 start-page: 15441 issue: 68 year: 2019 end-page: 15454 article-title: Circularly polarized luminescence switching in small organic molecules publication-title: Chem Eur J – volume: 114 start-page: 4496 issue: 8 year: 2014 end-page: 4539 article-title: Lanthanide probes for bioresponsive imaging publication-title: Chem Rev – volume: 120 start-page: 10145 issue: 18 year: 2020 end-page: 10243 article-title: Chiroptical properties in thin films of π‐conjugated systems publication-title: Chem Rev – volume: 8 start-page: 3284 issue: 10 year: 2020 end-page: 3301 article-title: Circularly polarized luminescence from AIEgens publication-title: J Mater Chem C – volume: 141 start-page: 18064 issue: 45 year: 2019 end-page: 18074 article-title: A [2]rotaxane‐based circularly polarized luminescence switch publication-title: J Am Chem Soc – volume: 142 start-page: 14432 issue: 34 year: 2020 end-page: 14436 article-title: Catalytic enantioselective synthesis and switchable chiroptical property of inherently chiral macrocycles publication-title: J Am Chem Soc – start-page: 325 year: 2020 end-page: 340 – volume: 453 year: 2022 article-title: Coordination‐based circularly polarized luminescence emitters: design strategy and application in sensing publication-title: Coord Chem Rev – volume: 12 start-page: 7491 issue: 31 year: 2021 end-page: 7496 article-title: Self‐assembly and circularly polarized luminescence from achiral pyrene–adamantane conjugates by selective inclusion with cyclodextrins publication-title: J Phys Chem Lett – volume: 27 start-page: 2920 issue: 9 year: 2021 end-page: 2934 article-title: Quantifying the overall efficiency of circularly polarized emitters publication-title: Chem Eur J – volume: 12 start-page: 8589 issue: 25 year: 2021 end-page: 8602 article-title: Pathways to increase the dissymmetry in the interaction of chiral light and chiral molecules publication-title: Chem Sci – volume: 6 issue: 1 year: 2022 article-title: Regulation of circularly polarized luminescence in multicomponent supramolecular coassemblies publication-title: ChemPhotoChem – volume: 142 start-page: 15661 issue: 37 year: 2020 end-page: 15666 article-title: Tetrameric and hexameric porphyrin nanorings: template synthesis and photophysical properties publication-title: J Am Chem Soc – volume: 51 start-page: 4094 issue: 7 year: 2012 end-page: 4098 article-title: Chiral sensing using an achiral europium(III) complex by induced circularly polarized luminescence publication-title: Inorg Chem – volume: 11 start-page: 6362 issue: 25 year: 2020 end-page: 6369 article-title: From reactive carbenes to chiral polyether macrocycles in two steps—synthesis and applications made easy? publication-title: Chem Sci – volume: 60 start-page: 15354 issue: 28 year: 2021 end-page: 15358 article-title: Hierarchical two‐level supramolecular chirality of an achiral anthracene‐based tetracationic nanotube in water publication-title: Angew Chem Int Ed – volume: 5 start-page: 1042 issue: 12 year: 2021 end-page: 1058 article-title: Circularly polarized luminescence in chiral π‐conjugated macrocycles publication-title: ChemPhotoChem – volume: 13 start-page: 611 issue: 3 year: 2022 end-page: 632 article-title: Chiral assembly of organic luminogens with aggregation‐induced emission publication-title: Chem Sci – year: 2020 – volume: 85 start-page: 1967 issue: 10 year: 2013 end-page: 1978 article-title: Recent progress in research on stimuli‐responsive circularly polarized luminescence based on π‐conjugated molecules publication-title: Pure Appl Chem – volume: 61 issue: 39 year: 2022 article-title: Chirality induction on a coordination capsule for circularly polarized luminescence publication-title: Angew Chem Int Ed – volume: 49 start-page: 1331 issue: 5 year: 2020 end-page: 1343 article-title: Recent advances in circularly polarized electroluminescence based on organic light‐emitting diodes publication-title: Chem Soc Rev – volume: 7 issue: 15 year: 2020 article-title: Axially chiral biphenyl compound‐based thermally activated delayed fluorescent materials for high‐performance circularly polarized organic light‐emitting diodes publication-title: Adv Sci – volume: 55 start-page: 1064 issue: 8 year: 2019 end-page: 1067 article-title: Chiroptical and catalytic properties of doubly binaphthyl‐strapped chiral porphyrins publication-title: Chem Commun – volume: 50 year: 2022 article-title: Advances in circularly polarized luminescent materials based on axially chiral compounds publication-title: J Photochem Photobiol C Photochem Rev – volume: 3 issue: 1 year: 2022 article-title: Adaptive helicity and chiral recognition in bright europium quadruple‐stranded helicates induced by host–guest interaction publication-title: Cell Rep Phys Sci – volume: 77 start-page: 773 issue: 6 year: 1977 end-page: 792 article-title: Circularly polarized luminescence spectroscopy publication-title: Chem Rev – volume: 1 start-page: 807 issue: 6 year: 2021 end-page: 818 article-title: Heterohelicenes through 1,3‐dipolar cycloaddition of sydnones with arynes: synthesis, origins of selectivity, and application to pH‐triggered chiroptical switch with CPL sign reversal publication-title: JACS Au – start-page: 9692 issue: 44 year: 2009 end-page: 9707 article-title: Luminescent chiral lanthanide(III) complexes as potential molecular probes publication-title: Dalton Trans – volume: 64 start-page: 2060 issue: 12 year: 2021 end-page: 2104 article-title: Frontiers in circularly polarized luminescence: molecular design, self‐assembly, nanomaterials, and applications publication-title: Sci China Chem – volume: 55 start-page: 13793 issue: 92 year: 2019 end-page: 13803 article-title: Advances in helicene derivatives with circularly polarized luminescence publication-title: Chem Commun – volume: 116 start-page: 13752 issue: 22 year: 2016 end-page: 13990 article-title: Supramolecular helical systems: helical assemblies of small molecules, foldamers, and polymers with chiral amplification and their functions publication-title: Chem Rev – volume: 24 start-page: 14613 issue: 55 year: 2018 end-page: 14616 article-title: Observation of circularly polarized luminescence of the excimer from two perylene cores in the form of [4]rotaxane publication-title: Chem Eur J – volume: 11 start-page: 2415 issue: 17 year: 2016 end-page: 2422 article-title: Chiral sensing of various amino acids using induced circularly polarized luminescence from europium(III) complexes of phenanthroline dicarboxylic acid derivatives publication-title: Chem Asian J – ident: e_1_2_5_79_1 doi: 10.1021/jacs.9b02582 – ident: e_1_2_5_42_1 doi: 10.1016/j.ccr.2021.214329 – ident: e_1_2_5_27_1 doi: 10.1007/978‐981‐15‐2309‐0 – ident: e_1_2_5_46_1 doi: 10.3390/molecules23123376 – ident: e_1_2_5_25_1 doi: 10.1007/978‐981‐15‐5085‐0_16 – ident: e_1_2_5_14_1 doi: 10.1021/acs.jpclett.5b01452 – ident: e_1_2_5_43_1 doi: 10.1016/j.ccr.2022.214640 – ident: e_1_2_5_52_1 doi: 10.1002/chem.201903252 – ident: e_1_2_5_39_1 doi: 10.1016/j.ccr.2019.06.017 – ident: e_1_2_5_11_1 doi: 10.1002/adma.202003615 – ident: e_1_2_5_69_1 doi: 10.1021/ja00209a033 – ident: e_1_2_5_80_1 doi: 10.1039/D1SC04403F – ident: e_1_2_5_18_1 doi: 10.1021/acs.chemrev.0c00195 – ident: e_1_2_5_94_1 doi: 10.1002/anie.202209340 – ident: e_1_2_5_4_1 doi: 10.1063/1.3582917 – ident: e_1_2_5_56_1 doi: 10.1021/jacs.8b01860 – ident: e_1_2_5_92_1 doi: 10.1002/anie.202205725 – ident: e_1_2_5_58_1 doi: 10.1021/jacs.0c05369 – ident: e_1_2_5_70_1 doi: 10.1021/acs.jpclett.1c02013 – ident: e_1_2_5_2_1 doi: 10.1021/cr60310a001 – ident: e_1_2_5_19_1 doi: 10.1016/j.ccr.2020.213329 – ident: e_1_2_5_77_1 doi: 10.1039/D1CC05902E – ident: e_1_2_5_61_1 doi: 10.1039/C6SC01808D – ident: e_1_2_5_13_1 doi: 10.1002/adma.202005760 – ident: e_1_2_5_47_1 doi: 10.1021/acs.chemrev.8b00770 – ident: e_1_2_5_34_1 doi: 10.1039/D0SC01011A – ident: e_1_2_5_57_1 doi: 10.1021/jacs.9b07143 – ident: e_1_2_5_53_1 doi: 10.1039/D0CS00191K – ident: e_1_2_5_16_1 doi: 10.1002/smll.201601455 – ident: e_1_2_5_21_1 doi: 10.1007/s11426‐021‐1146‐6 – ident: e_1_2_5_6_1 doi: 10.1002/anie.201800198 – ident: e_1_2_5_49_1 doi: 10.1002/chem.202002791 – ident: e_1_2_5_31_1 doi: 10.1021/acs.chemrev.0c01017 – ident: e_1_2_5_83_1 doi: 10.1021/ic500196m – ident: e_1_2_5_88_1 doi: 10.1039/C5CC08488A – ident: e_1_2_5_50_1 doi: 10.1039/D1SC02335G – ident: e_1_2_5_72_1 doi: 10.1002/anie.201408193 – ident: e_1_2_5_23_1 doi: 10.1039/D1SC02305E – ident: e_1_2_5_5_1 doi: 10.1021/cr400477t – ident: e_1_2_5_68_1 doi: 10.1021/ja00307a055 – ident: e_1_2_5_76_1 doi: 10.1002/anie.202108209 – ident: e_1_2_5_36_1 doi: 10.1002/cptc.202100228 – ident: e_1_2_5_78_1 doi: 10.1021/jacs.9b13184 – ident: e_1_2_5_65_1 doi: 10.1002/anie.202200727 – ident: e_1_2_5_81_1 doi: 10.1039/B909430J – ident: e_1_2_5_75_1 doi: 10.1002/anie.202105593 – ident: e_1_2_5_12_1 doi: 10.1002/adma.202008785 – ident: e_1_2_5_91_1 doi: 10.1021/jacs.0c07707 – ident: e_1_2_5_38_1 doi: 10.1002/chir.22382 – ident: e_1_2_5_64_1 doi: 10.1039/C9CC01138B – ident: e_1_2_5_35_1 doi: 10.1002/cptc.202100162 – ident: e_1_2_5_93_1 doi: 10.1016/j.chempr.2021.07.017 – ident: e_1_2_5_7_1 doi: 10.1002/adom.201800538 – ident: e_1_2_5_32_1 doi: 10.1016/j.jphotochemrev.2022.100500 – ident: e_1_2_5_20_1 doi: 10.1039/C9TC07022B – ident: e_1_2_5_28_1 doi: 10.1002/tcr.202100199 – ident: e_1_2_5_63_1 doi: 10.1021/acs.joc.8b00162 – ident: e_1_2_5_22_1 doi: 10.1002/cptc.202100124 – ident: e_1_2_5_48_1 doi: 10.3389/fchem.2020.00448 – ident: e_1_2_5_29_1 doi: 10.1016/j.mtchem.2021.100651 – ident: e_1_2_5_24_1 doi: 10.1002/cptc.202100256 – ident: e_1_2_5_26_1 doi: 10.1002/chem.201501178 – ident: e_1_2_5_67_1 doi: 10.1016/0009‐2614(81)80311‐9 – ident: e_1_2_5_17_1 doi: 10.1002/adma.201900110 – ident: e_1_2_5_10_1 doi: 10.1002/advs.202000804 – ident: e_1_2_5_73_1 doi: 10.1002/chem.201803215 – ident: e_1_2_5_15_1 doi: 10.1021/acs.chemrev.6b00354 – ident: e_1_2_5_84_1 doi: 10.1002/asia.201801777 – ident: e_1_2_5_45_1 doi: 10.1002/cptc.201800015 – ident: e_1_2_5_40_1 doi: 10.1016/j.chempr.2019.08.006 – ident: e_1_2_5_85_1 doi: 10.1002/asia.201600798 – ident: e_1_2_5_9_1 doi: 10.1021/acsami.9b20568 – ident: e_1_2_5_82_1 doi: 10.1021/ic202355s – ident: e_1_2_5_41_1 doi: 10.1021/acsomega.9b03613 – ident: e_1_2_5_44_1 doi: 10.1002/chir.22647 – ident: e_1_2_5_74_1 doi: 10.31635/ccschem.020.202000509 – ident: e_1_2_5_3_1 doi: 10.1021/cr00071a001 – ident: e_1_2_5_33_1 doi: 10.1016/j.tetlet.2019.151232 – ident: e_1_2_5_59_1 doi: 10.1021/jacsau.1c00084 – ident: e_1_2_5_62_1 doi: 10.1039/C8SC02935K – ident: e_1_2_5_30_1 doi: 10.1039/C9CC06861A – ident: e_1_2_5_66_1 doi: 10.1002/cptc.202100154 – ident: e_1_2_5_89_1 doi: 10.1002/slct.201800213 – ident: e_1_2_5_86_1 doi: 10.1039/C6DT01212D – ident: e_1_2_5_87_1 doi: 10.1016/j.xcrp.2021.100692 – ident: e_1_2_5_51_1 doi: 10.1351/PAC‐CON‐12‐11‐09 – ident: e_1_2_5_54_1 doi: 10.3389/fchem.2020.00458 – ident: e_1_2_5_55_1 doi: 10.1039/C6OB00752J – ident: e_1_2_5_8_1 doi: 10.1039/C9CS00680J – ident: e_1_2_5_71_1 doi: 10.1007/s10847‐021‐01108‐z – ident: e_1_2_5_90_1 doi: 10.1039/C8CC09114E – ident: e_1_2_5_37_1 doi: 10.1039/C2CS35242G – ident: e_1_2_5_60_1 doi: 10.1039/C6CC01277A |
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Snippet | Circularly polarized luminescence (CPL) dyes are recognized to be new generation materials and have been actively developed. Molecular recognition systems... |
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SubjectTerms | cage complexes Chemical perception Chemoreception chirality induction Circular polarization circularly polarized luminescence Coloring Agents Dyes host–guest complexes Luminescence macrocycles molecular recognition systems Recognition Stereoisomerism Supramolecular compounds Switches |
Title | Circularly polarized luminescence in molecular recognition systems: Recent achievements |
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