Yinuo Gu, Bo Li, Shuao Zhang, Shuhong Bao, Wenjie Yang, Wei Yang, Hongdian Lu, Chunxiang Wei, Man-Bo Li and San-E. Zhu
{"title":"一种pH稳定的氟-三苯胺光敏剂,具有高效的I型和II型ROS生成。","authors":"Yinuo Gu, Bo Li, Shuao Zhang, Shuhong Bao, Wenjie Yang, Wei Yang, Hongdian Lu, Chunxiang Wei, Man-Bo Li and San-E. Zhu","doi":"10.1039/D4OB02060J","DOIUrl":null,"url":null,"abstract":"<p >Photosensitizers (PSs) with robust pH stability and the ability to generate both type I and type II reactive oxygen species (ROS) have gained significant attention due to their versatility in various applications. In this study, we employed an electron donor–acceptor engineering strategy to design and synthesize a fluoran-triphenylamine photosensitizer (<strong>Fl-TPA</strong>), using an ester-protected ring-opened fluoran cation as the electron acceptor and triphenylamine (TPA) as the electron donor. Compared to fluoran with a spirolactone structure, <strong>Fl-TPA</strong> exhibits a significant redshift in absorption, with good light capture capabilities in the 300–600 nm range. In comparison with the reference compound <strong>Fl-H</strong>, which lacks the TPA group, <strong>Fl-TPA</strong> shows a substantial decrease in fluorescence intensity. Transient fluorescence measurements reveal biexponential decay characteristics for both compounds. Specifically, <strong>Fl-TPA</strong> shows <em>τ</em><small><sub>1</sub></small> = 0.21 ns (41%) and <em>τ</em><small><sub>2</sub></small> = 2.92 ns (59%), while <strong>Fl-H</strong> shows <em>τ</em><small><sub>1</sub></small> = 0.14 ns (93%) and <em>τ</em><small><sub>2</sub></small> = 2.23 ns (7%). The longer-lived component in <strong>Fl-TPA</strong> is more pronounced, suggesting the presence of additional non-radiative decay pathways, as further supported by the steady-state fluorescence analysis. Additionally, <strong>Fl-TPA</strong> exhibits a significant Stokes shift in solvents of varying polarity. Time-dependent density functional theory (TD-DFT) calculations reveal that the introduction of the strong electron-donating TPA group reduces the Δ<em>E</em><small><sub>S–T</sub></small> of <strong>Fl-TPA</strong> to 1.25 eV, which is significantly lower than that of <strong>Fl-H</strong> (1.46 eV), facilitating intersystem crossing (ISC). Thus, in the ROS generation experiment, it can be observed that <strong>Fl-H</strong> produces almost no ROS. In contrast, <strong>Fl-TPA</strong> not only exhibits high type I ROS generation capability, but also demonstrates excellent type II and total ROS generation capabilities, with performance far superior to the clinically approved near-infrared PS, indocyanine green (ICG). Moreover, <strong>Fl-TPA</strong> exhibits excellent pH stability compared to the non-esterified fluoran. The results of this study present a new photosensitizer with strong ROS generation capability and good stability across a wide pH range, providing a theoretical foundation for the design of PSs.</p>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":" 10","pages":" 2467-2479"},"PeriodicalIF":2.7000,"publicationDate":"2025-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A pH stable fluoran-triphenylamine photosensitizer with efficient type I and type II ROS generation†\",\"authors\":\"Yinuo Gu, Bo Li, Shuao Zhang, Shuhong Bao, Wenjie Yang, Wei Yang, Hongdian Lu, Chunxiang Wei, Man-Bo Li and San-E. Zhu\",\"doi\":\"10.1039/D4OB02060J\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Photosensitizers (PSs) with robust pH stability and the ability to generate both type I and type II reactive oxygen species (ROS) have gained significant attention due to their versatility in various applications. In this study, we employed an electron donor–acceptor engineering strategy to design and synthesize a fluoran-triphenylamine photosensitizer (<strong>Fl-TPA</strong>), using an ester-protected ring-opened fluoran cation as the electron acceptor and triphenylamine (TPA) as the electron donor. Compared to fluoran with a spirolactone structure, <strong>Fl-TPA</strong> exhibits a significant redshift in absorption, with good light capture capabilities in the 300–600 nm range. In comparison with the reference compound <strong>Fl-H</strong>, which lacks the TPA group, <strong>Fl-TPA</strong> shows a substantial decrease in fluorescence intensity. Transient fluorescence measurements reveal biexponential decay characteristics for both compounds. Specifically, <strong>Fl-TPA</strong> shows <em>τ</em><small><sub>1</sub></small> = 0.21 ns (41%) and <em>τ</em><small><sub>2</sub></small> = 2.92 ns (59%), while <strong>Fl-H</strong> shows <em>τ</em><small><sub>1</sub></small> = 0.14 ns (93%) and <em>τ</em><small><sub>2</sub></small> = 2.23 ns (7%). The longer-lived component in <strong>Fl-TPA</strong> is more pronounced, suggesting the presence of additional non-radiative decay pathways, as further supported by the steady-state fluorescence analysis. Additionally, <strong>Fl-TPA</strong> exhibits a significant Stokes shift in solvents of varying polarity. Time-dependent density functional theory (TD-DFT) calculations reveal that the introduction of the strong electron-donating TPA group reduces the Δ<em>E</em><small><sub>S–T</sub></small> of <strong>Fl-TPA</strong> to 1.25 eV, which is significantly lower than that of <strong>Fl-H</strong> (1.46 eV), facilitating intersystem crossing (ISC). Thus, in the ROS generation experiment, it can be observed that <strong>Fl-H</strong> produces almost no ROS. In contrast, <strong>Fl-TPA</strong> not only exhibits high type I ROS generation capability, but also demonstrates excellent type II and total ROS generation capabilities, with performance far superior to the clinically approved near-infrared PS, indocyanine green (ICG). Moreover, <strong>Fl-TPA</strong> exhibits excellent pH stability compared to the non-esterified fluoran. The results of this study present a new photosensitizer with strong ROS generation capability and good stability across a wide pH range, providing a theoretical foundation for the design of PSs.</p>\",\"PeriodicalId\":96,\"journal\":{\"name\":\"Organic & Biomolecular Chemistry\",\"volume\":\" 10\",\"pages\":\" 2467-2479\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-01-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic & Biomolecular Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/ob/d4ob02060j\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic & Biomolecular Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/ob/d4ob02060j","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
A pH stable fluoran-triphenylamine photosensitizer with efficient type I and type II ROS generation†
Photosensitizers (PSs) with robust pH stability and the ability to generate both type I and type II reactive oxygen species (ROS) have gained significant attention due to their versatility in various applications. In this study, we employed an electron donor–acceptor engineering strategy to design and synthesize a fluoran-triphenylamine photosensitizer (Fl-TPA), using an ester-protected ring-opened fluoran cation as the electron acceptor and triphenylamine (TPA) as the electron donor. Compared to fluoran with a spirolactone structure, Fl-TPA exhibits a significant redshift in absorption, with good light capture capabilities in the 300–600 nm range. In comparison with the reference compound Fl-H, which lacks the TPA group, Fl-TPA shows a substantial decrease in fluorescence intensity. Transient fluorescence measurements reveal biexponential decay characteristics for both compounds. Specifically, Fl-TPA shows τ1 = 0.21 ns (41%) and τ2 = 2.92 ns (59%), while Fl-H shows τ1 = 0.14 ns (93%) and τ2 = 2.23 ns (7%). The longer-lived component in Fl-TPA is more pronounced, suggesting the presence of additional non-radiative decay pathways, as further supported by the steady-state fluorescence analysis. Additionally, Fl-TPA exhibits a significant Stokes shift in solvents of varying polarity. Time-dependent density functional theory (TD-DFT) calculations reveal that the introduction of the strong electron-donating TPA group reduces the ΔES–T of Fl-TPA to 1.25 eV, which is significantly lower than that of Fl-H (1.46 eV), facilitating intersystem crossing (ISC). Thus, in the ROS generation experiment, it can be observed that Fl-H produces almost no ROS. In contrast, Fl-TPA not only exhibits high type I ROS generation capability, but also demonstrates excellent type II and total ROS generation capabilities, with performance far superior to the clinically approved near-infrared PS, indocyanine green (ICG). Moreover, Fl-TPA exhibits excellent pH stability compared to the non-esterified fluoran. The results of this study present a new photosensitizer with strong ROS generation capability and good stability across a wide pH range, providing a theoretical foundation for the design of PSs.
期刊介绍:
Organic & Biomolecular Chemistry is an international journal using integrated research in chemistry-organic chemistry. Founded in 2003 by the Royal Society of Chemistry, the journal is published in Semimonthly issues and has been indexed by SCIE, a leading international database. The journal focuses on the key research and cutting-edge progress in the field of chemistry-organic chemistry, publishes and reports the research results in this field in a timely manner, and is committed to becoming a window and platform for rapid academic exchanges among peers in this field. The journal's impact factor in 2023 is 2.9, and its CiteScore is 5.5.