Development of a Cholesteric Liquid Crystal Comprising a Mesogenic Fluorophore for Circularly Polarized Luminescence With a High Dissymmetry Factor

Yuuto Iida , Masayuki Gon , Hiroyuki Yoshida , Kazuo Tanaka , Gen-Ichi Konishi

Aggregate ›› 2026, Vol. 7 ›› Issue (3) : e70304

PDF (4281KB)
Aggregate ›› 2026, Vol. 7 ›› Issue (3) :e70304 DOI: 10.1002/agt2.70304
RESEARCH ARTICLE
Development of a Cholesteric Liquid Crystal Comprising a Mesogenic Fluorophore for Circularly Polarized Luminescence With a High Dissymmetry Factor
Author information +
History +
PDF (4281KB)

Abstract

Circularly polarized luminescence (CPL) has attracted considerable attention owing to its wide range of potential applications. Cholesteric liquid crystals (CLCs) are promising candidates for CPL-active materials because of their ease of fabrication, stimulus responsiveness, and ability to achieve high dissymmetry factors (|glum|). In most studies on CPL-active CLCs, non-mesogenic luminophores are doped into commercially available liquid crystals (LCs). However, their low solubility in LCs (typically only a few wt%) and their tendency to disrupt LC alignment present challenges in achieving high |glum| values—particularly in thin cells—and in broadening the CPL spectra. Here, we report a new LC mixture comprising our previously designed mesogenic fluorophore and a commercially available LC. This strategy enables a markedly increased luminophore loading (up to ∼50 wt%) and enhances the birefringence of the LC matrix. As a result, we achieved a notably high |glum| value of 1.25 even in thin cells (2 µm), together with significantly broadened CPL spectra. Furthermore, the emission wavelength was successfully tuned via Förster resonance energy transfer. This work demonstrates a rational design strategy for LC mixtures that yield CPL materials with high |glum|, advances the fundamental understanding of CPL generation in photoluminescent CLCs, and highlights their potential for future photonic and optoelectronic applications.

Keywords

circularly polarized luminescence / energy transfer / fluorescence / liquid crystals / self-assembly

Cite this article

Download citation ▾
Yuuto Iida, Masayuki Gon, Hiroyuki Yoshida, Kazuo Tanaka, Gen-Ichi Konishi. Development of a Cholesteric Liquid Crystal Comprising a Mesogenic Fluorophore for Circularly Polarized Luminescence With a High Dissymmetry Factor. Aggregate, 2026, 7 (3) : e70304 DOI:10.1002/agt2.70304

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

H. Tanaka, Y. Inoue, and T. Mori, “Circularly Polarized Luminescence and Circular Dichroisms in Small Organic Molecules: Correlation Between Excitation and Emission Dissymmetry Factors,” ChemPhotoChem 2 (2018): 386-402.

[2]

Y. Sang, J. Han, T. Zhao, P. Duan, and M. Liu, “Circularly Polarized Luminescence in Nanoassemblies: Generation, Amplification, and Application,” Advanced Materials 32 (2020): 1900110.

[3]

F. Zinna and L. D. Bari, “Lanthanide Circularly Polarized Luminescence: Bases and Applications,” Chirality 27 (2015): 1-13.

[4]

J. Roose and B. Z. Tang, “Circularly-Polarized Luminescence (CPL) From Chiral AIE Molecules and Macrostructures,” Small 12 (2016): 6495-6512.

[5]

M. Hasegawa, Y. Nojima, and Y. Mazaki, “Circularly Polarized Luminescence in Chiral π-Conjugated Macrocycles,” ChemPhotoChem 5 (2021): 1042-1058.

[6]

J.-Y. Wang, J.-W. Yuan, X.-M. Liu, et al., “Engineering Intelligent Chiral Silver Cluster-Assembled Materials for Temperature-Triggered Dynamic Circularly Polarized Luminescence,” Aggregate 5 (2024): e508.

[7]

Y. Li, J. Liang, S. Fu, et al., “Full-Color-Tunable Chiral Aggregation-Induced Emission Fluorophores With Tailored Propeller Chirality and Their Circularly Polarized Luminescence,” Aggregate 5 (2024): e613.

[8]

J. Jiang, Z. Ye, S. Zhang, et al., “α-Helix-Driven Regulation of Aqueous Circularly Polarized Luminescence in Homopolypeptide Self-Assembly,” Aggregate 6 (2025): e70123.

[9]

M. Zhang, Q. Guo, Z. Li, et al., “Processable Circularly Polarized Luminescence Material Enables Flexible Stereoscopic 3D Imaging,” Science Advances 9 (2023): eadi9944.

[10]

X. Zhan, F.-F. Xu, Z. Zhou, Y. Yan, J. Yao, and Y. S. Zhao, “3D Laser Displays Based on Circularly Polarized Lasing From Cholesteric Liquid Crystal Arrays,” Advanced Materials 33 (2021): 2104418.

[11]

W. Sun, B. Tian, B. An, et al., “Cellulose-Based Switchable Circularly Polarized Light Emitter: Photo-Actuated Chiral Assemblies With Azobenzene Polymers,” Aggregate 6 (2025): e712.

[12]

Y. Yang, R. da Costa, M. J. Fuchter, and A. J. Campbell, “Circularly Polarized Light Detection by a Chiral Organic Semiconductor Transistor,” Nature Photonics 7 (2013): 634-638.

[13]

C. Zhang, Z.-S. Li, X.-Y. Dong, Y.-Y. Niu, and S.-Q. Zang, “Multiple Responsive CPL Switches in an Enantiomeric Pair of Perovskite Confined in Lanthanide MOFs,” Advanced Materials 34 (2022): 2109496.

[14]

L. Zeng, C.-H. Guo, C. Li, et al., “Carbon-Nitrogen Axial Chirality as a Novel Chiral Framework Design Strategy for Circularly Polarized Luminescence Materials,” Aggregate 6 (2025): e70069.

[15]

W. Hong, Z. Yuan, and X. Chen, “Structural Color Materials for Optical Anticounterfeiting,” Small 16 (2020): 1907626.

[16]

L. Song, Y. Dong, B. Zhao, Y. Wu, and J. Deng, “Reversible Photochromism for Dynamically Tuning Full-Color Circularly Polarized Luminescence Toward Multi-Level Anti-Counterfeiting Application,” Advanced Optical Materials 12 (2024): 2400215.

[17]

W. Yuan, S. Lu, X. Li, et al., “Helically Assembled Rare Earth Fluoride Nanoparticles With Multicolor Circularly Polarized Luminescence for High-Security Anti-Counterfeiting,” Aggregate 6 (2025): e70042.

[18]

R. D. Richardson, M. G. J. Baud, C. E. Weston, H. S. Rzepa, M. K. Kuimova, and M. J. Fuchter, “Dual Wavelength Asymmetric Photochemical Synthesis With Circularly Polarized Light,” Chemical Science 6 (2015): 3853-3862.

[19]

Q. Li, S. Zheng, W. Gao, G. Zou, and Y. Cheng, “Circularly Polarized Ultraviolet Light-Activated Asymmetric Photopolymerization for the Synthesis of CPL-Active Materials,” Angewandte Chemie International Edition 64 (2025): e202503197.

[20]

M. Tsurui, Y. Kitagawa, K. Fushimi, M. Gon, K. Tanaka, and Y. Hasegawa, “Electronic Strain Effect on Eu(iii ) Complexes for Enhanced Circularly Polarized Luminescence,” Dalton Transactions 49 (2020): 5352.

[21]

M. Tsurui, Y. Kitagawa, S. Shoji, et al., “Asymmetric Lumino-Transformer: Circularly Polarized Luminescence of Chiral Eu(III) Coordination Polymer With Phase-Transition Behavior,” Journal of Physical Chemistry B 126 (2022): 3799-3807.

[22]

Y. Kitagawa, S. Wada, M. D. J. Islam, et al., “Chiral Lanthanide Lumino-Glass for a Circularly Polarized Light Security Device,” Communications Chemistry 3 (2020): 119.

[23]

H. Nishimura, K. Tanaka, Y. Morisaki, Y. Chujo, A. Wakamiya, and Y. Murata, “Oxygen-Bridged Diphenylnaphthylamine as a Scaffold for Full-Color Circularly Polarized Luminescent Materials,” Journal of Organic Chemistry 82 (2017): 5242-5249.

[24]

T. Zhang, Y. Zhang, Z. He, et al., “Recent Advances of Chiral Isolated and Small Organic Molecules: Structure and Properties for Circularly Polarized Luminescence,” Chemistry—An Asian Journal 19 (2024): e202400049.

[25]

M. Gon, Y. Morisaki, T. Sasamori, N. Tokitoh, and Y. Chujo, “Planar Chiral Tetrasubstituted [2.2]Paracyclophane: Optical Resolution and Functionalization,” Journal of the American Chemical Society 136 (2014): 3350.

[26]

M. Gon, Y. Morisaki, and Y. Chujo, “Optically Active Cyclic Compounds Based on Planar Chiral [2.2]Paracyclophane: Extension of the Conjugated Systems and Chiroptical Properties,” Journal of Materials Chemistry C 3 (2015): 521-529.

[27]

M. Gon, R. Sawada, Y. Morisaki, and Y. Chujo, “Enhancement and Controlling the Signal of Circularly Polarized Luminescence Based on a Planar Chiral Tetrasubstituted [2.2]Paracyclophane Framework in Aggregation System,” Macromolecules 50 (2017): 1790-1802.

[28]

M. Gon, Y. Morisaki, and Y. Chujo, “A Silver(I)-Induced Higher-Ordered Structure Based on Planar Chiral Tetrasubstituted [2.2]Paracyclophane,” Chemical Communications 53 (2017): 8304-8307.

[29]

K. Yuhara and K. Tanaka, “[7]Helicene-Appended o-Carboranes: Sign-Changing Circularly Polarized Luminescence Based on Dual-Emissive Properties and Its Temperature Dependency,” Advanced Optical Materials 14 (2025): e02647.

[30]

S. Tanaka, D. Sakamaki, N. Haruta, et al., “A double heterohelicene composed of two benzo[b]phenothiazine exhibiting intense room-temperature circularly polarized phosphorescence,” Journal of Materials Chemistry C 11 (2023): 4846-4854.

[31]

S. Sato, A. Yoshii, S. Takahashi, S. Furumi, M. Takeuchi, and H. Isobe, “Chiral Intertwined Spirals and Magnetic Transition Dipole Moments Dictated by Cylinder Helicity,” Proceedings of the National Academy of Sciences of the United States of America 114 (2017): 13097-13101.

[32]

K. Matsumura, R. Inoue, and Y. Morisaki, “Optically Active A-Shaped Cyclic Molecules Based on Planar Chiral [2.2]Paracyclophanes Emitting Bright Circularly Polarized Luminescence With High Anisotropy Factors,” Advanced Functional Materials 34 (2024): 2310566.

[33]

Y. Sawada, S. Furumi, A. Takai, M. Takeuchi, K. Noguchi, and K. Tanaka, “Rhodium-Catalyzed Enantioselective Synthesis, Crystal Structures, and Photophysical Properties of Helically Chiral 1,1′-Bitriphenylenes,” Journal of the American Chemical Society 134 (2012): 4080-4083.

[34]

F. Morita, Y. Kishida, Y. Sato, et al., “Design and Enantioselective Synthesis of 3D π-Extended Carbohelicenes for Circularly Polarized Luminescence,” Nature Synthesis 3 (2024): 774-786.

[35]

H. Yan, Y. He, D. Wang, T. Han, and B. Z. Tang, “Aggregation-Induced Emission Polymer Systems With Circularly Polarized Luminescence,” Aggregate 4 (2023): e331.

[36]

Y. Morisaki, R. Hifumi, L. Lin, K. Inoshita, and Y. Chujo, “Through-Space Conjugated Polymers Consisting of Planar Chiral Pseudo-Ortho-Linked [2.2]Paracyclophane,” Polymer Chemistry 3 (2012): 2727-2730.

[37]

S. Fukao and M. Fujiki, “Circularly Polarized Luminescence and Circular Dichroism From Si−Si-Bonded Network Polymers,” Macromolecules 42 (2009): 8062.

[38]

H. Zhong, B. Zhao, and J. Deng, “Polymer-Based Circularly Polarized Luminescent Materials,” Advanced Optical Materials 11 (2023): 2202787.

[39]

Q. Song, X. Meng, S. Liu, et al., “Helical Assembly of Long-Chain Unsubstituted Poly(Para -Phenylene) Immobilized on Individual Cellulose Nanocrystals,” Aggregate 6 (2025): e70206.

[40]

J. Kumar, T. Nakashima, and T. Kawai, “Circularly Polarized Luminescence in Chiral Molecules and Supramolecular Assemblies,” Journal of Physical Chemistry Letters 6 (2015): 3445-3452.

[41]

K. Kato, R. Iwano, S. Tokuda, et al., “Circularly Polarized Luminescence From a Common Alkoxy Pillar[5]Arene and Its Co-Aggregates With π-Conjugated Rods,” Aggregate 5 (2024): e482.

[42]

Y. Hou, C. Mu, Y. Shi, et al., “Host-Guest Complexation-Induced Chirality Switching of Pillararenes by Perylene Diimide-Based Hexagonal Metallacages,” Aggregate 5 (2024): e628.

[43]

W. Zhang, M.-Q. Liu, and Y. Luo, “Chiral Amplification and Regulation: Design and Applications of Circularly Polarized Luminescence-Active Materials Derived From Macrocyclic Compounds,” Aggregate 6 (2025): e70039.

[44]

X. Tong, J. Wang, M. Wei, et al., “High-Performance Optical Stimuli-Responsive Circularly Polarized Luminescence Induced by Chiral CsPbBr 3 Nanoparticles in Achiral MOFs,” Aggregate 6 (2025): e70188.

[45]

Y. Wu, M. Li, Z.-G. Zheng, Z.-Q. Yu, and W.-H. Zhu, “Liquid Crystal Assembly for Ultra-Dissymmetric Circularly Polarized Luminescence and Beyond,” Journal of the American Chemical Society 145 (2023): 12951-12966.

[46]

W. Kang, Y. Tang, X. Meng, et al., “A Photo- and Thermo-Driven Azoarene-Based Circularly Polarized Luminescence Molecular Switch in a Liquid Crystal Host,” Angewandte Chemie International Edition 62 (2023): e20231146.

[47]

J. Liu, Z.-P. Song, L.-Y. Sun, B.-X. Li, Y.-Q. Lu, and Q. Li, “Circularly Polarized Luminescence in Chiral Orientationally Ordered Soft Matter Systems,” Responsive Materials 2 (2023): e20230005.

[48]

Y. Chen, Y. Zhang, H. Li, et al., “Dynamic Circularly Polarized Luminescence With Tunable Handedness and Intensity Enabled by Achiral Dichroic Dyes in Cholesteric Liquid Crystal Medium,” Advanced Materials 34 (2022): 2202309.

[49]

J. Yuan, X. Lu, and Q. Lu, “Large-Scale Chiral Spherulites With Controllable Circularly Polarized Luminescence in Liquid Crystal Block Copolymers Film,” Aggregate 5 (2024): e431.

[50]

M. Li, H. Hu, B. Liu, et al., “Light-Reconfiguring Inhomogeneous Soft Helical Pitch With Fatigue Resistance and Reversibility,” Journal of the American Chemical Society 144 (2022): 20773-20784.

[51]

X. Liu, C. Yuan, P. Sun, Z. Na, H. Hu, and Z. G. Zheng, “Programming Dual-Color Circularly Polarized Luminescence With Self-Organized Soft Photonic Helix,” Laser & Photonics Reviews 18 (2024): 2300603.

[52]

X. Li, Q. Li, Y. Wang, Y. Quan, D. Chen, and Y. Cheng, “Strong Aggregation-Induced CPL Response Promoted by Chiral Emissive Nematic Liquid Crystals (N*-LCs),” Chemistry: A European Journal 24 (2018): 12607-12612.

[53]

S. Suzuki, K. Kaneko, T. Hanasaki, M. Shizuma, and Y. Imai, “Circularly Polarized Luminescence Switching of Chiral Perylene Diimide-Doped Nematic Liquid Crystal Using DC Electric Field,” ChemPhotoChem 8 (2024): e202300224.

[54]

K. Terakubo, H. Nakajima, D. Suzuki, K. Kaneko, T. Hanasaki, and Y. Imai, “Control of Circularly Polarized Luminescence in Extended Π-Electronic Aromatics-Based Chiral Liquid Crystals Induced by Electric Fields,” ChemPhotoChem 9 (2025): e202500112.

[55]

B. A. S. Jose, J. Yan, and K. Akagi, “Dynamic Switching of the Circularly Polarized Luminescence of Disubstituted Polyacetylene by Selective Transmission Through a Thermotropic Chiral Nematic Liquid Crystal,” Angewandte Chemie International Edition 53 (2014): 10641-10644.

[56]

S. Liu, X. Liu, Y. Wu, et al., “Circularly Polarized Perovskite Luminescence With Dissymmetry Factor Up to 1.9 by Soft Helix Bilayer Device,” Matter 5 (2022): 2319-2333.

[57]

X. Wang, B. Zhao, and J. Deng, “Liquid Crystals Doped With Chiral Fluorescent Polymer: Multi-Color Circularly Polarized Fluorescence and Room-Temperature Phosphorescence With High Dissymmetry Factor and Anti-Counterfeiting Application,” Advanced Materials 35 (2023): 2304405.

[58]

M. Mitov, “Cholesteric Liquid Crystals With a Broad Light Reflection Band,” Advanced Materials 24 (2012): 6260-6276.

[59]

D. K. Yang, J. W. Doane, Z. Yaniv, and J. Glasser, “Cholesteric Reflective Display: Drive Scheme and Contrast,” Applied Physics Letters 64 (1994): 1905-1907.

[60]

J. Li, H. K. Bisoyi, J. Tian, J. Guo, and Q. Li, “Optically Rewritable Transparent Liquid Crystal Displays Enabled by Light-Driven Chiral Fluorescent Molecular Switches,” Advanced Materials 31 (2019): 1807751.

[61]

H. Coles and S. Morris, “Liquid-Crystal Lasers,” Nature Photonics 4 (2010): 676-685.

[62]

H. Yoshida, C. H. Lee, Y. Matsuhisa, A. Fujii, and M. Ozaki, “Bottom-Up Fabrication of Photonic Defect Structures in Cholesteric Liquid Crystals Based on Laser-Assisted Modification of the Helix,” Advanced Materials 19 (2007): 1187-1190.

[63]

Y. Watanabe, M. Uchimura, F. Araoka, G. Konishi, J. Watanabe, and H. Takezoe, “Extremely Low Threshold in a Pyrene-Doped Distributed Feedback Cholesteric Liquid Crystal Laser,” Applied Physics Express 2 (2009): 102501.

[64]

Y. Inoue, H. Yoshida, K. Inoue, et al., “Tunable Lasing From a Cholesteric Liquid Crystal Film Embedded With a Liquid Crystal Nanopore Network,” Advanced Materials 23 (2011): 5498-5501.

[65]

S. Cho, H. Yoshida, and M. Ozaki, “Emission Direction-Tunable Liquid Crystal Laser,” Advanced Optical Materials 8 (2020): 2000375.

[66]

Y. Inoue, H. Yoshida, H. Kuno, and M. Ozaki, “Deformation-Free, Microsecond Electro-Optic Tuning of Liquid Crystals,” Advanced Optical Materials 1 (2013): 256-263.

[67]

D. Zhao, H. He, X. Gu, et al., “Circularly Polarized Luminescence and a Reflective Photoluminescent Chiral Nematic Liquid Crystal Display Based on an Aggregation-Induced Emission Luminogen,” Advanced Optical Materials 4 (2016): 534-539.

[68]

K. Horie, Y. Fujita, K. Kaneko, T. Hanasaki, and K. Akagi, “Thermally Invertible Full-Color Circularly Polarized Luminescence With High Dissymmetry Factors and High Quantum Yields in Fluorene Derivatives With Induced Chirality Generated in Chiral Liquid Crystals,” ACS Applied Materials & Interfaces 17 (2025): 15988-15999.

[69]

J. Yan, F. Ota, B. A. S. Jose, and K. Akagi, “Chiroptical Resolution and Thermal Switching of Chirality in Conjugated Polymer Luminescence via Selective Reflection Using a Double-Layered Cell of Chiral Nematic Liquid Crystal,” Advanced Functional Materials 27 (2017): 1604529.

[70]

Q. Ye, D. Zhu, H. Zhang, X. Li, and Q. Li, “Thermally Tunable Circular Dichroism and Circularly Polarized Luminescence of Tetraphenylethene With Two Cholesterol Pendants,” Journal of Materials Chemistry C 3 (2015): 6997-7003.

[71]

Y. Chen, P. Lu, Q. Gui, Z. Li, Y. Yuan, and H. Zhang, “Preparation of Chiral Luminescent Liquid Crystals and Manipulation Effect of Phase Structures on the Circularly Polarized Luminescence Property,” Journal of Materials Chemistry C 9 (2021): 1279-1286.

[72]

Z.-W. Luo, A. Huang, H.-Y. Luo, J.-K. Chen, J. Huang, and H.-L. Xie, “Regulating Circularly Polarized Luminescent Behavior of Luminescent Liquid Crystalline Polymers Through Resonance Energy Transfer,” Macromolecules 56 (2023): 2700-2708.

[73]

W. Gong, G. Huang, Y. Yuan, and H. Zhang, “Strong and Multicolor-Tunable Pure Organic Circularly Polarized Room-Temperature Phosphorescence From Cholesteric Liquid Crystal,” Advanced Optical Materials 11 (2023): 2300745.

[74]

Y. Wu, L. H. You, Z.-Q. Yu, et al., “Rational Design of Circularly Polarized Luminescent Aggregation-Induced Emission Luminogens (AIEgens): Promoting the Dissymmetry Factor and Emission Efficiency Synchronously,” ACS Materials Letters 2 (2020): 505-510.

[75]

W. Shen, H. Zhang, Z. Miao, and Z. Ye, “Recent Progress in Functional Dye-Doped Liquid Crystal Devices,” Advanced Functional Materials 33 (2023): 2210664.

[76]

M. T. Sims, “Dyes as Guests in Ordered Systems: Current Understanding and Future Directions,” Liquid Crystals 43 (2016): 2364-2374.

[77]

J. Voskuhl and M. Giese, “Mesogens With Aggregation-Induced Emission Properties: Materials With a Bright Future,” Aggregate 3 (2022): e124.

[78]

D. Zhao, F. Fan, J. Cheng, et al., “Light-Emitting Liquid Crystal Displays Based on an Aggregation-Induced Emission Luminogen,” Advanced Optical Materials 3 (2015): 199-202.

[79]

M. Uchimura, Y. Watanabe, F. Araoka, J. Watanabe, H. Takezoe, and G. Konishi, “Development of Laser Dyes to Realize Low Threshold in Dye-Doped Cholesteric Liquid Crystal Lasers,” Advanced Materials 22 (2010): 4473-4478.

[80]

S. P. Yadav, K. K. Pandey, A. K. Misra, P. K. Tripathi, and R. Manohar, “The Molecular Ordering Phenomenon in Dye-Doped Nematic Liquid Crystals,” Physica Scripta 83 (2011): 035704.

[81]

Z.-W. Lio, L. Tao, C.-L. Zhong, et al., “High-Efficiency Circularly Polarized Luminescence From Chiral Luminescent Liquid Crystalline Polymers With Aggregation-Induced Emission Properties,” Macromolecules 53 (2020): 9758-9768.

[82]

W. Zhang, C. Zhang, K. Chen, et al., “Synthesis and Characterisation of Liquid Crystalline Anthraquinone Dyes With Excellent Dichroism and Solubility,” Liquid Crystals 43 (2016): 1307-1314.

[83]

X. Li, Y. Shen, K. Liu, Y. Quan, and Y. Cheng, “Recyclable CPL Switch Regulated by Using an Applied DC Electric Field From Chiral Nematic Liquid Crystals (N*-LCs),” Materials Chemistry Frontiers 4 (2020): 2954-2961.

[84]

D. Suzuki, K. Kaneko, and Y. Imai, “Electric Field-Induced Circularly Polarised Luminescence Switching in Chiral Nematic Liquid Crystals With Negative Dielectric Anisotropy,” Physical Chemistry Chemical Physics 27 (2025): 21867-21870.

[85]

Y.-C. Yang, R. S. Zola, Y. Cui, et al., “30.3: Master Parameter Governing the Response Time of Reflective Cholesteric Liquid Crystal Displays,” SID Symposium Digest of Technical Papers 42 (2011): 400-403.

[86]

S. Huang, Q. Wu, R. Luo, B. Tan, Y. Yuan, and H. Zhang, “Tunable Helix Inversion and Circularly Polarized Luminescence in Cholesteric Liquid Crystal Copolymers With Room-Temperature Phosphorescence,” Macromolecules 57 (2024): 9017-9029.

[87]

M. Zhou, P. Zeng, Y. Yuan, and H. Zhang, “Liquid Crystal Phase Structure and Conformation Engineering in Polymers Enables Highly Efficient and Tunable Circularly Polarized Luminescence,” European Polymer Journal 236 (2025): 114170.

[88]

M. Voigt, M. Chambers, and M. Grell, “On the Circular Polarization of Fluorescence From Dyes Dissolved in Chiral Nematic Liquid Crystals,” Chemical Physics Letters 347 (2001): 173-177.

[89]

S. H. Chen, D. Katsis, A. W. Schmid, J. C. Mastrangelo, T. Tsutsui, and T. N. Blanton, “Circularly Polarized Light Generated by Photoexcitation of Luminophores in Glassy Liquid-crystal Films,” Nature 397 (1999): 506-508.

[90]

H. Shi, B. M. Conger, D. Katsis, and S. H. Chen, “Circularly Polarized Fluorescence From Chiral Nematic Liquid Crystalline Films: Theory and Experiment,” Liquid Crystals 24 (1998): 163-172.

[91]

P. V. Dolganov, K. D. Baklanova, and V. K. Dolganov, “Spectral and Polarization Characteristics of the Light Passing Through a Cholesteric Photonic Crystal,” Journal of Experimental and Theoretical Physics 130 (2020): 790-796.

[92]

A. T. Phillips, J. D. Hoang, and T. J. White, “Helical Pitch and Thickness-Dependent Opto-Mechanical Response in Cholesteric Liquid Crystal Elastomers,” Soft Matter 21 (2025): 2160-2169.

[93]

D.-K. Yang and Q. Li, “Color Reflective LCD Based on Cholesteric Liquid Crystals,” in High Quality Liquid Crystal Displays and Smart Devices, ed. S. Ishihara, S. Kobayashi, and Y. Ukai (The Institution of Engineering and Technology, 2004), 167.

[94]

Y. Iida, Y. Shimomura, M. Tokita, and G. Konishi, “Push-Pull Biphenyl and Tolane Derivatives as Novel Luminescent Liquid Crystals: Synthesis and Properties,” Liquid Crystals 51 (2024): 2032-2045.

[95]

R. Yamaguchi, K. Moriyama, and S. Sato, “Improvement of White Fluorescent Liquid Crystal Display,” Molecular Crystals & Liquid Crystals 488 (2008): 210-218.

[96]

S. Jeon, B. Kim, H. Ye, and S.-K. Hong, “Full Colour Reflective Display Using Photoluminescence-Polymer Dispersed Liquid Crystal,” Molecular Crystals & Liquid Crystals 597 (2014): 159-166.

[97]

R. Yamaguchi, J. Kishida, and S. Sato, “Multicolor Switching Properties in Fluorescent Liquid Crystal Displays,” Japanese Journal of Applied Physics 39 (2000): 5235.

[98]

Y. Shimomura, Y. Iida, E. Tsurumaki, and G. Konishi, “Innovative Molecular Design of Bridged Biphenyls for Calamitic Nematic Liquid Crystals With Extensive π-Conjugated Mesogens,” Materials Chemistry Frontiers 9 (2025): 1127-1138.

[99]

T. Ikeda, S. Kurihara, and S. Tazuke, “Excimer Formation Kinetics in Liquid-Crystalline Alkylcyanobiphenyls,” Journal of Physical Chemistry 94 (1990): 6550-6555.

[100]

R. Subramanian, L. K. Patterson, and H. Levanon, “Luminescence Behavior as a Probe for Phase Transitions and Excimer Formation in Liquid Crystals: Dodecylcyanobiphenyl,” Chemical Physics Letters 93 (1982): 578-581.

[101]

T. K. Sarbaz, M. Zakerhamidi, B. Rezaei, and A. Ranjkesh, “Experimental Elucidation of Nematic Host-Driven Modulation of Bragg Reflection in Cholesteric Liquid Crystals,” Optical Materials 169 (2026): 117576.

[102]

M. F. Vuks, “Multicolor Switching Properties in Fluorescent Liquid Crystal Displays,” Optics and Spectroscopy 20 (1966): 361.

[103]

E. Sackmann and J. Voss, “Circular Dichroism of Helically Arranged Molecules in Cholesteric Phases,” Chemical Physics Letters 14 (1972): 528-532.

[104]

G. Bunt and F. S. Wouters, “FRET From Single to Multiplexed Signaling Events,” Biophysical Reviews 9 (2017): 119-129.

[105]

L. Olejko and I. Bald, “FRET Efficiency and Antenna Effect in Multi-Color DNA Origami-Based Light Harvesting Systems,” RSC Advances 7 (2017): 23924-23934.

[106]

C. D. Luca, E. C. Galleposo, R. R. Ferreira, et al., “Benzoyl-Xanthenoxanthenes: Versatile Chromophores for Light-Engaging Applications,” Angewandte Chemie International Edition 65 (2026): e23349.

[107]

R. Iwai, H. Yoshida, Y. Arakawa, et al., “Near-Room-Temperature π-Conjugated Nematic Liquid Crystals in Molecules With a Flexible Seven-Membered Ring Structure,” Aggregate 6 (2025): e660.

[108]

R. Iwai, S. Suzuki, S. Sasaki, et al., “Bridged Stilbenes: AIEgens Designed via a Simple Strategy to Control the Non-Radiative Decay Pathway,” Angewandte Chemie International Edition 59 (2020): 10566-10573.

[109]

A. Hori, A. Matsumoto, J. Ikenouchi, and G. Konishi, “D−π-A Fluorophores With Strong Solvatochromism for Single-Molecule Ratiometric Thermometers,” Journal of the American Chemical Society 147 (2025): 9953-9961.

[110]

T. Tanaka, A. Matsumoto, E. Tsurumaki, J. Ikenouchi, and G. Konishi, “Fluorescent Solvatochromic Probes for Long-Term Imaging of Lipid Order in Living Cells,” Advanced Science 11 (2024): 2309721.

RIGHTS & PERMISSIONS

2026 The Author(s). Aggregate published by SCUT, AIEI, and John Wiley & Sons Australia, Ltd.

PDF (4281KB)

0

Accesses

0

Citation

Detail

Sections
Recommended

/