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。

IF 2.7 3区 化学 Q1 CHEMISTRY, ORGANIC
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}
引用次数: 0

摘要

光敏剂(ps)具有强大的pH稳定性和产生I型和II型活性氧(ROS)的能力,由于其在各种应用中的通用性而受到了极大的关注。在本研究中,我们采用电子给受体工程策略,以酯保护的开环氟离子为电子受体,三苯胺(TPA)为电子给体,设计并合成了氟-三苯胺光敏剂(Fl-TPA)。与具有螺内酯结构的氟烷相比,Fl-TPA在吸收中表现出明显的红移,在300-600 nm范围内具有良好的光捕获能力。与缺少TPA基团的参比化合物Fl-H相比,Fl-TPA的荧光强度明显降低。瞬态荧光测量揭示了这两种化合物的双指数衰减特性。其中,Fl-TPA的τ1 = 0.21 ns(41%)和τ2 = 2.92 ns (59%), Fl-H的τ1 = 0.14 ns(93%)和τ2 = 2.23 ns(7%)。Fl-TPA中寿命较长的成分更为明显,表明存在额外的非辐射衰变途径,这一点得到了稳态荧光分析的进一步支持。此外,Fl-TPA在不同极性的溶剂中表现出明显的斯托克斯位移。时间依赖密度泛函理论(TD-DFT)计算表明,强给电子基团TPA的引入使Fl-TPA的ΔES-T降至1.25 eV,显著低于Fl-H的1.46 eV,有利于系统间交叉(ISC)。因此,在ROS生成实验中,可以观察到Fl-H几乎不产生ROS。相比而言,Fl-TPA不仅具有较高的I型ROS生成能力,而且具有优异的II型和总ROS生成能力,其性能远优于临床批准的近红外PS吲哚菁绿(ICG)。此外,与未酯化的氟烷相比,Fl-TPA具有优异的pH稳定性。本研究结果提出了一种新的光敏剂,具有较强的ROS生成能力和较宽pH范围内的良好稳定性,为ps的设计提供了理论基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A pH stable fluoran-triphenylamine photosensitizer with efficient type I and type II ROS generation†

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.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry 化学-有机化学
CiteScore
5.50
自引率
9.40%
发文量
1056
审稿时长
1.3 months
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信