Tuning the Properties of Hydrazone/Isosorbide-Based Switchable Chiral Dopants DOI

Brandon Balamut,

Russell P. Hughes, Ivan Aprahamian

et al.

Journal of the American Chemical Society, Journal Year: 2024, Volume and Issue: 146(35), P. 24561 - 24569

Published: Aug. 20, 2024

The long-range supramolecular interactions in liquid crystals (LCs) can be used to amplify and subsequently propagate microscopic structural changes into macroscopic events. Here, we report on a systematic structure–property analysis using 16 chiral photoswitchable dopants composed of bistable hydrazones isosorbide moieties. Our findings showcase the relationship between dopant's structure its helical twisting power (β), hence, photophysical properties host LC. We show that an increase hydrazone CNNH dihedral angle results β value, while alkoxy chains do not lead such increase. These contradict established rules thumb, stating rigidity long alky are needed for high values. also found position substitution, whether at 2′ or 5′ positions unit, attachment unit rotor stator phenyl units have negative positive additive effects either decrease made us hypothesize unsymmetrically functionalized should result large Δβ values, which corroborated experimentally. Moreover, fluorine-functionalized dopant resulted higher overall most likely because π–π interactions. Finally, were modulating locking reflective LC films, yielding multicolor canvases reflect light from ultraviolet infrared range (i.e., manipulation up ca. 1500 nm reflected light).

Language: Английский

A Photo‐ and Thermo‐Driven Azoarene‐Based Circularly Polarized Luminescence Molecular Switch in a Liquid Crystal Host DOI Open Access
W.P. Kang, Yuqi Tang, Xianyu Meng

et al.

Angewandte Chemie International Edition, Journal Year: 2023, Volume and Issue: 62(48)

Published: Aug. 31, 2023

The development of chiral optical active materials with switchable circularly polarized luminescence (CPL) signals remains a challenge. Here an azoarene-based molecular switch, (S, R, S)-switch 1 and (R, R)-switch 2, are designed prepared (R)-binaphthyl azo group as photosensitive moiety two (S)- or fluorescent molecules opposite the same handedness moieties. Both switches exhibit reversible trans/cis isomerization when irradiated by 365 nm UV light 520 green in solvent liquid crystal (LC) media. In contrast control switch is doped into nematic LCs, polarization inversion switching-off CPL achieved resultant helical superstructure upon irradiation light, respectively. Meanwhile, fluorescence intensity system basically unchanged during this switching process. particular, these variations could be recovered after heating, realizing true sense switching. Taking advantage unique switching, proof-of-concept for "a dual-optical information encryption system" based on above material demonstrated.

Language: Английский

Citations

67

Responsive soft actuators with MXene nanomaterials DOI Creative Commons

Shaoshuai Ma,

Pan Xue,

Yuqi Tang

et al.

Deleted Journal, Journal Year: 2023, Volume and Issue: 2(1)

Published: Dec. 11, 2023

Abstract Compared with traditional rigid actuators, soft actuators exhibit a large number of advantages, including enhanced flexibility, reconfigurability, and adaptability, which motivate us to develop artificial widespread applications. Soft MXene nanomaterials are regarded as highly promising candidates for advancing the development bioinspired robotics consequence their unprecedented physicochemical characteristics, such high electronic conductivity, thermal photothermal conversion capability, abundant surface functional groups. Herein, comprehensive overview recent advancement extensive applications from perspective bioinspiration is provided. First, synthetic methods properties briefly summarized. Subsequently, (including photoresponsive electroresponsive chemoresponsive actuators) sequentially investigated focus on fabrication approaches, actuation properties, underlying mechanisms, At end, future challenges opportunities rapid discussed.

Language: Английский

Citations

44

When quantum dots meet blue phase liquid crystal elastomers: visualized full-color and mechanically-switchable circularly polarized luminescence DOI Creative Commons
Shan Li, Yuqi Tang,

Qingyan Fan

et al.

Light Science & Applications, Journal Year: 2024, Volume and Issue: 13(1)

Published: June 14, 2024

Abstract Polymer-based circularly polarized luminescence (CPL) materials with the advantage of diversified structure, easy fabrication, high thermal stability, and tunable properties have garnered considerable attention. However, adequate precise tuning over CPL in polymer-based remains challenging due to difficulty regulating chiral structures. Herein, visualized full-color is achieved by doping red, green, blue quantum dots (QDs) into reconfigurable phase liquid crystal elastomers (BPLCEs). In contrast signal observed cholesteric (CLCEs), 3D cubic superstructure BPLCEs induces an opposite signal. Notably, this effect entirely independent photonic bandgaps (PBGs) results a g lum value, even without matching between PBGs emission bands QDs. Meanwhile, lattice structure can be reversibly switched via mechanical stretching force, inducing on-off switching signals, these variations further fixed using dynamic disulfide bonds BPLCEs. Moreover, smart systems for anti-counterfeiting information encryption been demonstrated, suggesting great potential BPLCEs-based active materials.

Language: Английский

Citations

34

Dynamically Modulating the Dissymmetry Factor of Circularly Polarized Organic Ultralong Room‐Temperature Phosphorescence from Soft Helical Superstructures DOI
Jiao Liu,

Junjie Wu,

Juan Wei

et al.

Angewandte Chemie International Edition, Journal Year: 2024, Volume and Issue: 63(12)

Published: Jan. 24, 2024

Abstract Achieving circularly polarized organic ultralong room‐temperature phosphorescence (CP‐OURTP) with a high luminescent dissymmetry factor (g lum ) is crucial for diverse optoelectronic applications. In particular, dynamically controlling the of CP‐OURTP can profoundly advance these applications, but it still unprecedented. This study introduces an effective strategy to achieve photoirradiation‐driven chirality regulation in bilayered structure film, which consists layer soft helical superstructure incorporated light‐driven molecular motor and phosphorescent (RTP) polymer. The prepared film exhibits emission lifetime 805 ms g value up 1.38. Remarkably, resulting be reversibly controlled between 0.6 1.38 over 20 cycles by light irradiation, representing first example CP‐OURTP.

Language: Английский

Citations

29

Assembly‐Induced Dynamic Structural Color in a Host‐Guest System for Time‐Dependent Anticounterfeiting and Double‐Lock Encryption DOI

Yufan Ji,

Tianfu Song, Haifeng Yu

et al.

Angewandte Chemie International Edition, Journal Year: 2024, Volume and Issue: 63(26)

Published: April 10, 2024

Manipulation of periodic micro/nanostructures in polymer film is great importance for academics and industrial applications anticounterfeiting. However, with the increasing demand on information security, materials time-dependent features are urgently required, especially material where same can appear more than once time scale. Here, one concise strategy to realize anticounterfeiting "double-lock" encryption based a host-guest system proposed, photoresponsive azopolymer as host liquid-crystalline molecule guest. The exhibits tunable mass transport pre-designed by tailoring process cis-to-trans recovery azo groups assembly mesogenic trans-isomers, resulting dynamic structural color film. Taking advantage this extraordinary feature, has been achieved. More importantly, each state's appearance whole be modulated changing ratio. Combining manipulatable unique decoding method, stored decrypted correctly. This work provides an unprecedented approach advanced technology higher level security high-end encryption.

Language: Английский

Citations

16

Inversion of Molecular Chirality Associated with Ferroelectric Switching in a High-Temperature Two-Dimensional Perovskite Ferroelectric DOI

Wen-Feng Deng,

Yuxia Li, Yanxin Zhao

et al.

Journal of the American Chemical Society, Journal Year: 2023, Volume and Issue: 145(9), P. 5545 - 5552

Published: Feb. 24, 2023

Controlling molecular chirality by external stimuli is of great significance in both fundamental research and technological applications. Herein, we report a high-temperature (384 K) ferroelectric Cu(II) complex whose spontaneous polarization can be switched associated with flipping chirality. In this two-dimensional perovskite structure, the inorganic layer separated (NH3(CH2)2SS(CH2)2NH3)2+ organic cations skewed chiral conformation (P- or M-helicity an individual crystal). As stereodynamic disulfide bridge determines dipole moment along polar axis, cation converted to its enantiomer as consequence electric field-induced shift S-S moiety relative screw axis during switching. The variation examined single-crystal X-ray diffraction circular dichroism spectra. simultaneous switching may lead novel electronic phenomena.

Language: Английский

Citations

38

Stimuli‐responsive active materials for dynamic control of light field DOI Creative Commons

Ren Zheng,

Yang Wei,

Zichen Zhang

et al.

Deleted Journal, Journal Year: 2023, Volume and Issue: 1(2)

Published: Oct. 19, 2023

Abstract The increasing demand for the multidimensional and dynamic control of light has spurred development stimuli‐responsive, reconfigurable, programmable optical systems. Liquid crystals (LCs), which combine liquid‐like stimuli‐responsiveness crystal‐like orientational ordering, have emerged as highly appealing soft materials. Owing to their exceptional performance functionalities, they are becoming incredibly important materials in active planar optics photonics. Additionally, silk proteins, luminescent materials, metasurfaces exhibit properties, enabling remarkable multifunctional applications. This review focuses on advancements stimuli‐responsive including LCs, well some these paired with LCs. Their attractive tunable applications photonics, along great potential future systems, also emphasized.

Language: Английский

Citations

36

An ultrawide-range photochromic molecular fluorescence emitter DOI Creative Commons
Xiao Chen, Xiaofang Hou, Xu‐Man Chen

et al.

Nature Communications, Journal Year: 2024, Volume and Issue: 15(1)

Published: June 26, 2024

Abstract Photocontrollable luminescent molecular switches capable of changing emitting color have been regarded as the ideal integration between intelligent and materials. A remaining challenge is to combine good luminescence properties with wide range wavelength transformation, especially when confined in a single system that forms well-defined nanostructures. Here, we report π-expanded photochromic photoswitch, which allows for comprehensive achievements including emission variation (240 nm wide, 400–640 nm), high photoisomerization extent (95%), pure (<100 full width at half maximum). We take advantageous mechanism modulating self-assembly intramolecular charge transfer synthesis construction, further realize by simple photocontrol. Based on this, both photoactivated anti-counterfeiting function self-erasing photowriting films are achieved fluorescence. This work will provide insight into design optical

Language: Английский

Citations

14

Robust, Ultrafast and Reversible Photoswitching in Bulk Polymers Enabled by Octupolar Molecule Design DOI
Long Fang, Zi-Wei Lin, Yang Zhang

et al.

Angewandte Chemie International Edition, Journal Year: 2024, Volume and Issue: 63(16)

Published: Feb. 13, 2024

Abstract Improving the photoswitching rate and robustness of photochromic molecules in bulk solids is paramount for practical applications but remains an on‐going challenge. Here, we introduce octupolar design paradigm to develop a new family visible light organic photoswitches, namely multi‐branched Stenhouse Adducts (MOPSAs) featuring C 3 ‐symmetrical A ‐(D‐core) architecture with dipolar donor–acceptor (D–A) photochrome each branch. Our couples multi‐dimensional geometric electronic effects MOPSAs enable robust ultrafast reversible polymers. Specifically, optimal MOPSA (4 wt %) commercial polyurethane films accomplishes nearly 100 % discoloration 6 s under ∼ thermal‐recovery 17.4 at 60 °C, while acquired kinetics constants are 3∼7 times that DASA counterpart 1∼2 orders magnitude higher than those reported DASAs Importantly, MOPSA‐doped polymer sustain 500 discoloration/recovery cycles slow degradation, superior existing polymers (≤30 cycles). We discover multi‐dipolar coupling enables enhanced polarization electron delocalization, promoting rate‐determining thermal cyclization, branched non‐planar geometry induces large free volume facilitate isomerization. This can be extended spiropyran or azobenzene‐based films. The performance together their high‐yield scalable synthesis facile film processing inspires us explore versatile uses as smart inks labels time‐temperature indicators, optical logic encryption multi‐levelled data encryption.

Language: Английский

Citations

12

Chiral structures in azobenzene‐containing systems: Construction, regulation, and application DOI Creative Commons

Zixiang He,

Xiaoxiao Cheng, Zhao Wang

et al.

Deleted Journal, Journal Year: 2024, Volume and Issue: 2(2)

Published: May 1, 2024

Abstract Chirality is a fundamental property in nature, which essential for the existence and survival of living organisms. Smart responsive chiroptical materials have garnered increasing attention due to their unique structural characteristics potential applications. Among these, azobenzene (Azo), as typical photoresponsive chromophore, plays crucial role constructing controlling chiral structures. The cis ‐ trans isomerization, liquid crystallinity, other physicochemical properties allow wide range tunability stimuli‐responsive materials. Herein, we review research studies field chiral/achiral Azo building blocks multilevel generation well switching, summarize recent advances on applications structures from micro macro levels. Finally, aim provide an overview challenges new opportunities development novel smart

Language: Английский

Citations

12