{"title":"第一个基于荧光素的六链间质的合成及其自组装性质","authors":"Xiaoling Xie, Xiaoqin Yi, Yurun Liang, Jun Leng, Xiaotong Liu, Hongfei Gao, Yulong Xiao","doi":"10.1080/15421406.2023.2258695","DOIUrl":null,"url":null,"abstract":"AbstractFirst series of fluorescein-based hexacatenar mesogens consisting of a central fluorescein unit and two 1,2,3-triazole dendritic wings were designed and synthesized by using the Williamson reaction and Cu-assisted alkyne-azide cycloaddition reaction. Polarized optical microscopy textures, differential scanning calorimetry curves, and X-ray diffraction (XRD) data demonstrated that all the compounds can self-assemble into hexagonal columnar mesophases. Organogel test demonstrated that these compounds could form organogel in some moderate polar solvents with irregularly winkled morphologies. Density functional theory calculation demonstrated that these mesogens adopted distorted conformation which might be the reason why narrow mesogenic temperature ranges and irregularly winkled morphologies in these compounds are observed.Keywords: Fluoresceinhexacatenarliquid crystalorganogel AcknowledgmentsWe thank beamline 1W2A at Beijing Synchrotron Radiation Facility (BSRF), China.Disclosure statementNo potential conflict of interest was reported by the authors.Additional informationFundingThis work was supported by China West Normal University Doctor Startup Fund (No. 412821), Major project funds of Chemical Synthesis and Pollution Control Key Laboratory of Sichuan Province (No. CSPC202101), The Science and Technology Department of Sichuan Province (No. 2022NSFSC1237), Natural Science Foundation of China (No. 22265030), and Funds for leading local scientific technological development by the central government (202307AB110010).","PeriodicalId":18758,"journal":{"name":"Molecular Crystals and Liquid Crystals","volume":"134 1","pages":"0"},"PeriodicalIF":0.7000,"publicationDate":"2023-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis and self-assembly properties of the first fluorescein-based hexacatenar mesogens\",\"authors\":\"Xiaoling Xie, Xiaoqin Yi, Yurun Liang, Jun Leng, Xiaotong Liu, Hongfei Gao, Yulong Xiao\",\"doi\":\"10.1080/15421406.2023.2258695\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"AbstractFirst series of fluorescein-based hexacatenar mesogens consisting of a central fluorescein unit and two 1,2,3-triazole dendritic wings were designed and synthesized by using the Williamson reaction and Cu-assisted alkyne-azide cycloaddition reaction. Polarized optical microscopy textures, differential scanning calorimetry curves, and X-ray diffraction (XRD) data demonstrated that all the compounds can self-assemble into hexagonal columnar mesophases. Organogel test demonstrated that these compounds could form organogel in some moderate polar solvents with irregularly winkled morphologies. Density functional theory calculation demonstrated that these mesogens adopted distorted conformation which might be the reason why narrow mesogenic temperature ranges and irregularly winkled morphologies in these compounds are observed.Keywords: Fluoresceinhexacatenarliquid crystalorganogel AcknowledgmentsWe thank beamline 1W2A at Beijing Synchrotron Radiation Facility (BSRF), China.Disclosure statementNo potential conflict of interest was reported by the authors.Additional informationFundingThis work was supported by China West Normal University Doctor Startup Fund (No. 412821), Major project funds of Chemical Synthesis and Pollution Control Key Laboratory of Sichuan Province (No. CSPC202101), The Science and Technology Department of Sichuan Province (No. 2022NSFSC1237), Natural Science Foundation of China (No. 22265030), and Funds for leading local scientific technological development by the central government (202307AB110010).\",\"PeriodicalId\":18758,\"journal\":{\"name\":\"Molecular Crystals and Liquid Crystals\",\"volume\":\"134 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.7000,\"publicationDate\":\"2023-09-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular Crystals and Liquid Crystals\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/15421406.2023.2258695\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Crystals and Liquid Crystals","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/15421406.2023.2258695","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Synthesis and self-assembly properties of the first fluorescein-based hexacatenar mesogens
AbstractFirst series of fluorescein-based hexacatenar mesogens consisting of a central fluorescein unit and two 1,2,3-triazole dendritic wings were designed and synthesized by using the Williamson reaction and Cu-assisted alkyne-azide cycloaddition reaction. Polarized optical microscopy textures, differential scanning calorimetry curves, and X-ray diffraction (XRD) data demonstrated that all the compounds can self-assemble into hexagonal columnar mesophases. Organogel test demonstrated that these compounds could form organogel in some moderate polar solvents with irregularly winkled morphologies. Density functional theory calculation demonstrated that these mesogens adopted distorted conformation which might be the reason why narrow mesogenic temperature ranges and irregularly winkled morphologies in these compounds are observed.Keywords: Fluoresceinhexacatenarliquid crystalorganogel AcknowledgmentsWe thank beamline 1W2A at Beijing Synchrotron Radiation Facility (BSRF), China.Disclosure statementNo potential conflict of interest was reported by the authors.Additional informationFundingThis work was supported by China West Normal University Doctor Startup Fund (No. 412821), Major project funds of Chemical Synthesis and Pollution Control Key Laboratory of Sichuan Province (No. CSPC202101), The Science and Technology Department of Sichuan Province (No. 2022NSFSC1237), Natural Science Foundation of China (No. 22265030), and Funds for leading local scientific technological development by the central government (202307AB110010).
期刊介绍:
Established in 1966, Molecular Crystals and Liquid Crystals is a world-leading journal publishing original research papers in both an experimental and theoretical nature in three areas of specialization: liquid crystals, molecular crystals, and low-dimensional solids. These cover, but are not limited to:
Liquid Crystals:
-Electro- and magneto-optical phenomena; thermodynamics; phase transitions; structure; NMR and orientation-controlled spectroscopy; theory.
Molecular Crystals:
-Spectroscopy; energy and charge transfer; solid state reactions; photo and radiation effects
Low-dimensional Solids:
-Structure, electronic, magnetic, and optical properties; transport mechanisms
The journal publishes research papers, review papers, and book reviews. In all three areas, experimental manuscripts describing both preparation and properties will be considered. Papers that describe determination of crystal structure alone are not encouraged unless some solid state forces (hydrogen bonding, charge transfer, etc.) are playing a significant role and/or some solid state properties of the materials are measured.