{"title":"柱[5]芳烃和非那嗪的自组装使基于fret的VOCs检测成为可能","authors":"Guo-Yan Liang, Shao-Ping Tao, Bing-Bing Shi, Qi Lin, Jin-Fa Chen, Tai-Bao Wei","doi":"10.1016/j.jphotochem.2025.116807","DOIUrl":null,"url":null,"abstract":"<div><div>With Pyridine (<strong>Py</strong>) and Tetrahydrofuran (<strong>THF</strong>) being listed as class 2B carcinogens by the World Health Organization, and considering their extensive use as volatile organic solvents (VOCs), detection of <strong>Py</strong> and <strong>THF</strong> is critically important. This study introduced a novel sensing platform <strong>CP[5]A@G</strong> based on Förster resonance energy transfer (FRET) system to successfully realized the detection of these two toxic gasses. The sensing platform <strong>CP[5]A@G</strong> was developed through supramolecular self-assembly between the coumarin-modified pillar[5]arene (<strong>CP[5]A</strong>) and phenazine derivative (<strong>G</strong>). In which, the <strong>CP[5]A</strong> acted as host molecule and energy donor, accordingly, the <strong>G</strong> acted as the guest molecule and energy acceptor. This platform <strong>CP[5]A@G</strong> exhibited significant aggregation-caused quenching (ACQ) effects in chloroform and n-hexane mixed solvent. Generally speaking, ACQ effect is untoward for luminescence properties of organic compounds and is more severe in the solid state. However, based on the ACQ property of platform <strong>CP[5]A@G</strong>, we have realized the detection of <strong>Py</strong> and <strong>THF</strong> in solvent and film states through the host-guest competitive assembly and lone pair···π interaction mechanisms. The responses were manifested in the opening and quenching effects on the fluorescence luminescence. These findings represent substantial advancements in the adsorption of <strong>Py</strong> and <strong>THF</strong>, with promising applications in commercial gas recognition systems and sensor design.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"472 ","pages":"Article 116807"},"PeriodicalIF":4.7000,"publicationDate":"2025-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Self-assembly of Pillar[5]arene and phenazine enables FRET-based VOCs detection\",\"authors\":\"Guo-Yan Liang, Shao-Ping Tao, Bing-Bing Shi, Qi Lin, Jin-Fa Chen, Tai-Bao Wei\",\"doi\":\"10.1016/j.jphotochem.2025.116807\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>With Pyridine (<strong>Py</strong>) and Tetrahydrofuran (<strong>THF</strong>) being listed as class 2B carcinogens by the World Health Organization, and considering their extensive use as volatile organic solvents (VOCs), detection of <strong>Py</strong> and <strong>THF</strong> is critically important. This study introduced a novel sensing platform <strong>CP[5]A@G</strong> based on Förster resonance energy transfer (FRET) system to successfully realized the detection of these two toxic gasses. The sensing platform <strong>CP[5]A@G</strong> was developed through supramolecular self-assembly between the coumarin-modified pillar[5]arene (<strong>CP[5]A</strong>) and phenazine derivative (<strong>G</strong>). In which, the <strong>CP[5]A</strong> acted as host molecule and energy donor, accordingly, the <strong>G</strong> acted as the guest molecule and energy acceptor. This platform <strong>CP[5]A@G</strong> exhibited significant aggregation-caused quenching (ACQ) effects in chloroform and n-hexane mixed solvent. Generally speaking, ACQ effect is untoward for luminescence properties of organic compounds and is more severe in the solid state. However, based on the ACQ property of platform <strong>CP[5]A@G</strong>, we have realized the detection of <strong>Py</strong> and <strong>THF</strong> in solvent and film states through the host-guest competitive assembly and lone pair···π interaction mechanisms. The responses were manifested in the opening and quenching effects on the fluorescence luminescence. These findings represent substantial advancements in the adsorption of <strong>Py</strong> and <strong>THF</strong>, with promising applications in commercial gas recognition systems and sensor design.</div></div>\",\"PeriodicalId\":16782,\"journal\":{\"name\":\"Journal of Photochemistry and Photobiology A-chemistry\",\"volume\":\"472 \",\"pages\":\"Article 116807\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2025-09-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Photochemistry and Photobiology A-chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1010603025005477\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Photochemistry and Photobiology A-chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1010603025005477","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Self-assembly of Pillar[5]arene and phenazine enables FRET-based VOCs detection
With Pyridine (Py) and Tetrahydrofuran (THF) being listed as class 2B carcinogens by the World Health Organization, and considering their extensive use as volatile organic solvents (VOCs), detection of Py and THF is critically important. This study introduced a novel sensing platform CP[5]A@G based on Förster resonance energy transfer (FRET) system to successfully realized the detection of these two toxic gasses. The sensing platform CP[5]A@G was developed through supramolecular self-assembly between the coumarin-modified pillar[5]arene (CP[5]A) and phenazine derivative (G). In which, the CP[5]A acted as host molecule and energy donor, accordingly, the G acted as the guest molecule and energy acceptor. This platform CP[5]A@G exhibited significant aggregation-caused quenching (ACQ) effects in chloroform and n-hexane mixed solvent. Generally speaking, ACQ effect is untoward for luminescence properties of organic compounds and is more severe in the solid state. However, based on the ACQ property of platform CP[5]A@G, we have realized the detection of Py and THF in solvent and film states through the host-guest competitive assembly and lone pair···π interaction mechanisms. The responses were manifested in the opening and quenching effects on the fluorescence luminescence. These findings represent substantial advancements in the adsorption of Py and THF, with promising applications in commercial gas recognition systems and sensor design.
期刊介绍:
JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds.
All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor).
The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.