Fengqing Hu, Siao Shi, Shijie Yang, Jiayan Zhao, Dou Liu, Xinyue Zhang, Yuxiang Wang and Fei Li
{"title":"由静电和芳烃-全氟芳烃相互作用触发的手性超分子模板中的活化圆偏振发光","authors":"Fengqing Hu, Siao Shi, Shijie Yang, Jiayan Zhao, Dou Liu, Xinyue Zhang, Yuxiang Wang and Fei Li","doi":"10.1039/D5TC02799C","DOIUrl":null,"url":null,"abstract":"<p >The approaches to the generation of circularly polarized luminescence (CPL) signals have attracted much interest due to the potential application of CPL materials in information encryption and three-dimensional displays. However, most strategies mainly depend on the rational design and complicated synthesis of chiral fluorophores, highlighting the great significance of developing a facile and novel strategy for designing CPL materials. Herein, we employed the classical benzene-1,3,5-tricarboxamide-based chiral compound <strong><em>D</em>/<em>L</em>-cC<small><sub>3</sub></small></strong> as a supramolecular template to co-assemble with a pyrene-based fluorophore (<strong>Py0</strong> or <strong>Py1</strong>) and octafluoronaphthalene (<strong>OFN</strong>). The supramolecular template <strong><em>D</em>/<em>L</em>-cC<small><sub>3</sub></small></strong> could not effectively induce the chirality of Py derivatives through electrostatic interactions. Importantly, chiral optical properties emerged in the ternary co-assembly system <strong><em>D</em>/<em>L</em>-cC<small><sub>3</sub></small>-Py1-OFN</strong> through electrostatic and arene–perfluoroarene (AP) interactions, with a |<em>g</em><small><sub>lum</sub></small>| value of 5.1 × 10<small><sup>−3</sup></small>. These findings reveal that the chiral induction from a chiral supramolecular template to an achiral fluorophore may be ineffective through electrostatic interaction, and the joint effect of electrostatic and AP interactions provides a facile way for the generation of CPL properties.</p>","PeriodicalId":84,"journal":{"name":"Journal of Materials Chemistry C","volume":" 41","pages":" 20973-20978"},"PeriodicalIF":5.1000,"publicationDate":"2025-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Activated circularly polarized luminescence in a chiral supramolecular template triggered by electrostatic and arene–perfluoroarene interactions\",\"authors\":\"Fengqing Hu, Siao Shi, Shijie Yang, Jiayan Zhao, Dou Liu, Xinyue Zhang, Yuxiang Wang and Fei Li\",\"doi\":\"10.1039/D5TC02799C\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The approaches to the generation of circularly polarized luminescence (CPL) signals have attracted much interest due to the potential application of CPL materials in information encryption and three-dimensional displays. However, most strategies mainly depend on the rational design and complicated synthesis of chiral fluorophores, highlighting the great significance of developing a facile and novel strategy for designing CPL materials. Herein, we employed the classical benzene-1,3,5-tricarboxamide-based chiral compound <strong><em>D</em>/<em>L</em>-cC<small><sub>3</sub></small></strong> as a supramolecular template to co-assemble with a pyrene-based fluorophore (<strong>Py0</strong> or <strong>Py1</strong>) and octafluoronaphthalene (<strong>OFN</strong>). The supramolecular template <strong><em>D</em>/<em>L</em>-cC<small><sub>3</sub></small></strong> could not effectively induce the chirality of Py derivatives through electrostatic interactions. Importantly, chiral optical properties emerged in the ternary co-assembly system <strong><em>D</em>/<em>L</em>-cC<small><sub>3</sub></small>-Py1-OFN</strong> through electrostatic and arene–perfluoroarene (AP) interactions, with a |<em>g</em><small><sub>lum</sub></small>| value of 5.1 × 10<small><sup>−3</sup></small>. These findings reveal that the chiral induction from a chiral supramolecular template to an achiral fluorophore may be ineffective through electrostatic interaction, and the joint effect of electrostatic and AP interactions provides a facile way for the generation of CPL properties.</p>\",\"PeriodicalId\":84,\"journal\":{\"name\":\"Journal of Materials Chemistry C\",\"volume\":\" 41\",\"pages\":\" 20973-20978\"},\"PeriodicalIF\":5.1000,\"publicationDate\":\"2025-09-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Materials Chemistry C\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/tc/d5tc02799c\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Materials Chemistry C","FirstCategoryId":"1","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/tc/d5tc02799c","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
Activated circularly polarized luminescence in a chiral supramolecular template triggered by electrostatic and arene–perfluoroarene interactions
The approaches to the generation of circularly polarized luminescence (CPL) signals have attracted much interest due to the potential application of CPL materials in information encryption and three-dimensional displays. However, most strategies mainly depend on the rational design and complicated synthesis of chiral fluorophores, highlighting the great significance of developing a facile and novel strategy for designing CPL materials. Herein, we employed the classical benzene-1,3,5-tricarboxamide-based chiral compound D/L-cC3 as a supramolecular template to co-assemble with a pyrene-based fluorophore (Py0 or Py1) and octafluoronaphthalene (OFN). The supramolecular template D/L-cC3 could not effectively induce the chirality of Py derivatives through electrostatic interactions. Importantly, chiral optical properties emerged in the ternary co-assembly system D/L-cC3-Py1-OFN through electrostatic and arene–perfluoroarene (AP) interactions, with a |glum| value of 5.1 × 10−3. These findings reveal that the chiral induction from a chiral supramolecular template to an achiral fluorophore may be ineffective through electrostatic interaction, and the joint effect of electrostatic and AP interactions provides a facile way for the generation of CPL properties.
期刊介绍:
The Journal of Materials Chemistry is divided into three distinct sections, A, B, and C, each catering to specific applications of the materials under study:
Journal of Materials Chemistry A focuses primarily on materials intended for applications in energy and sustainability.
Journal of Materials Chemistry B specializes in materials designed for applications in biology and medicine.
Journal of Materials Chemistry C is dedicated to materials suitable for applications in optical, magnetic, and electronic devices.
Example topic areas within the scope of Journal of Materials Chemistry C are listed below. This list is neither exhaustive nor exclusive.
Bioelectronics
Conductors
Detectors
Dielectrics
Displays
Ferroelectrics
Lasers
LEDs
Lighting
Liquid crystals
Memory
Metamaterials
Multiferroics
Photonics
Photovoltaics
Semiconductors
Sensors
Single molecule conductors
Spintronics
Superconductors
Thermoelectrics
Topological insulators
Transistors