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Chiral perovskites typically exhibit efficient circular dichroism and circularly polarized luminescence, demonstrating promising applications in chiroptical and spintronic devices. However, the relationship between the chiroptical properties and structurally symmetric elements of chiral perovskites has not been established. The unique structure of the high-fold axis may impart distinctive chiral optoelectronic properties, yet it remains unexplored. Here, we have successfully constructed a pair of chiral perovskite enantiomers with both 6-fold screw and 3-fold rotation axes. Enantiomeric enrichment was achieved by employing a chiral induction strategy. Their chiroptical properties were systematically investigated by circular dichroism. Furthermore, systematic theoretical calculations were conducted to reveal the mechanism of chirality transfer and the Rashba splitting, which compensate for the adverse influence of chiral distortion on carrier transport. Our work offers a novel strategy to construct high-fold axial chiral perovskites and bridges the knowledge gap between their crystal structures and their chiroptical properties.
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http://dx.doi.org/10.1021/acs.nanolett.5c02909 | DOI Listing |
ACS Appl Mater Interfaces
September 2025
State Key Laboratory of Chemical Resource Engineering, Beijing 100029, China.
Circularly polarized luminescence (CPL) has emerged as a critical technology for anticounterfeiting and optical display applications due to its unique chiroptical properties. We report a multicolor CPL-emitting elastomeric film (P37/PSK@SiO-PDMS) that synergistically combines chiral helical polyacetylene (P37) and a surface-engineered perovskite (PSK@SiO) through hydrogen-bond-directed assembly. Confinement within the PDMS matrix drives P37 to self-assemble into a chiral supramolecular structure through hydrogen bonding, inducing a chiroptical inversion.
View Article and Find Full Text PDFOrg Lett
September 2025
Max Planck Institute of Microstructure Physics, Weinberg 2, 06120 Halle, Germany.
Helical nanographenes (NGs) play a crucial role in the development of chiral nanomaterials due to their distinctive optoelectronic and chiroptical properties. Herein, we report the efficient synthesis of two unprecedented azulene-embedded asymmetric triple helical NGs ( and ) with controllable helicene subunit lengths and π-extension. The crystallographic analysis confirms their highly twisted and asymmetric geometries.
View Article and Find Full Text PDFCarbohydr Polym
November 2025
Molecular Imaging and Photonics, Department of Chemistry, KU Leuven, Campus Kulak Kortrijk, Etienne Sabbelaan 53, 8500 Kortrijk, Belgium. Electronic address:
Cellulose nanocrystals (CNCs) have emerged as promising candidates for chiroptical functional materials due to their ability to form cholesteric liquid crystals with tunable periodicity. The quality of the final cholesteric phase is influenced by the nucleation, growth and coalescence mechanism of the initial droplets, known as tactoids. Current research focuses on understanding the size and morphological transformations of these tactoids, to gain deeper insights into their dynamic behavior and, in turn, to better control the final properties of novel photonic materials.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
State Key Laboratory of Functional Crystals and Devices, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian, 350002, P.R. China.
Chiral metal halide perovskites (CMHPs) are a promising class of chiroptical materials with significant potential applications in chiral-optoelectronic and chiral-spintronic devices. However, their chirality induction generally stems from the incorporation of chiral ligands, which constitutes compositional diversity and functional versatility. Herein, we report a significant chiral expression resulting from two distinct mechanisms: chirality transfer induced by chiral organic cations and mirror symmetry breaking driven by stereochemically active lone pairs, both contributing to controlled chirality induction.
View Article and Find Full Text PDFChemistry
September 2025
Department of Chemistry, School of Science, Institute of Science Tokyo, 2-12-1 Ookayama, Meguro-ku, Tokyo, 152-8551, Japan.
Expanded helicenes are interesting compounds created by modifying the original helicene structure through the incorporation of linearly fused benzene rings, enlarging the helical diameter. Motivated by Tilley et al.'s report of a key expanded helicene structure in 2017, several research groups have synthesized such nonplanar aromatic compounds, aiming to explore their impressive structures, properties, and chiroptical performance.
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