• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

2-(2'-氨基苯基)苯并噻唑衍生物的化学性质:合成、光物理性质及应用

Chemistry of 2-(2'-Aminophenyl)benzothiazole Derivatives: Syntheses, Photophysical Properties and Applications.

作者信息

Pylova Ekaterina K, Sukhikh Taisiya S, Prieto Alexis, Jaroschik Florian, Konchenko Sergey N

机构信息

Nikolaev Institute of Inorganic Chemistry, Siberian Branch of the Russian Academy of Sciences, 3 Lavrentiev Ave., 630090 Novosibirsk, Russia.

Department of Natural Sciences, Novosibirsk State University, 630090 Novosibirsk, Russia.

出版信息

Molecules. 2025 Apr 8;30(8):1659. doi: 10.3390/molecules30081659.

DOI:10.3390/molecules30081659
PMID:40333580
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12029770/
Abstract

2-(2'-aminophenyl)benzothiazole is a readily tunable fluorescent core with widespread applications in coordination chemistry, sensing, light-emitting processes, medicinal chemistry, and catalysis. This review provides an overview of the synthetic methodologies to access 2-(2'-aminophenyl)benzothiazole and its organic derivatives, including various phosphorous and silane pincer ligands. The luminescent properties will be discussed, with a special focus on ESIPT and AIE processes. The coordination of transition metals and lanthanides is presented, as well as their influence on biological and light-emitting properties. 2-(2'-aminophenyl)benzothiazole derivatives have also been employed as sensors for a range of cations and anions due to their various binding modes, as well as for bioimaging purposes. Recently, the first application in photocatalysis has emerged, showing one of the many openings for these organic building blocks in the future.

摘要

2-(2'-氨基苯基)苯并噻唑是一种易于调节的荧光核心,在配位化学、传感、发光过程、药物化学和催化等领域有着广泛的应用。本文综述了合成2-(2'-氨基苯基)苯并噻唑及其有机衍生物的方法,包括各种磷和硅烷钳形配体。将讨论其发光性质,特别关注激发态分子内质子转移(ESIPT)和聚集诱导发光(AIE)过程。介绍了过渡金属和镧系元素的配位情况,以及它们对生物和发光性质的影响。由于2-(2'-氨基苯基)苯并噻唑衍生物具有多种结合模式,它们还被用作一系列阳离子和阴离子的传感器,以及用于生物成像。最近,其在光催化方面的首次应用已经出现,这显示出这些有机结构单元在未来有众多的发展机遇。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/2208e27fe415/molecules-30-01659-sch018.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/c487d3dbea5f/molecules-30-01659-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/e1c55095e304/molecules-30-01659-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/b49f6234a6bd/molecules-30-01659-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/e574392cc843/molecules-30-01659-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/f892113d0f6f/molecules-30-01659-sch003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/7d70690dc38d/molecules-30-01659-sch004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/2443eea504ff/molecules-30-01659-sch005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/1878ae8df45d/molecules-30-01659-sch006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/475c05106827/molecules-30-01659-sch007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/4838a41e7f97/molecules-30-01659-sch008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/b10b279b3896/molecules-30-01659-sch009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/334bd7e5dbe8/molecules-30-01659-sch010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/355355e63950/molecules-30-01659-sch011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/5ce7a79ef6fd/molecules-30-01659-sch012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/d4a94700c8c3/molecules-30-01659-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/827cbf56d335/molecules-30-01659-sch013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/1f4e53239cff/molecules-30-01659-sch014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/1715bad1dafa/molecules-30-01659-sch015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/8426850ebe9d/molecules-30-01659-sch016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/5ffb8719887b/molecules-30-01659-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/a23eea2e003e/molecules-30-01659-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/a447ab5a5889/molecules-30-01659-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/debb9df7d787/molecules-30-01659-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/3b480d9df84f/molecules-30-01659-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/f031a2fe9f4e/molecules-30-01659-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/d3356883c27a/molecules-30-01659-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/afcfa4d72ca8/molecules-30-01659-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/506299992572/molecules-30-01659-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/2b7e84f71e0a/molecules-30-01659-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/28bd78b0d1a4/molecules-30-01659-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/24cd6d894626/molecules-30-01659-g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/b836a8b31701/molecules-30-01659-g016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/57aabd067145/molecules-30-01659-g017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/633146a09cfe/molecules-30-01659-sch017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/1e0580bdb00a/molecules-30-01659-g018.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/e172f1dea19a/molecules-30-01659-g019.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/fece5e54f1f4/molecules-30-01659-g020.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/2208e27fe415/molecules-30-01659-sch018.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/c487d3dbea5f/molecules-30-01659-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/e1c55095e304/molecules-30-01659-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/b49f6234a6bd/molecules-30-01659-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/e574392cc843/molecules-30-01659-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/f892113d0f6f/molecules-30-01659-sch003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/7d70690dc38d/molecules-30-01659-sch004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/2443eea504ff/molecules-30-01659-sch005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/1878ae8df45d/molecules-30-01659-sch006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/475c05106827/molecules-30-01659-sch007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/4838a41e7f97/molecules-30-01659-sch008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/b10b279b3896/molecules-30-01659-sch009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/334bd7e5dbe8/molecules-30-01659-sch010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/355355e63950/molecules-30-01659-sch011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/5ce7a79ef6fd/molecules-30-01659-sch012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/d4a94700c8c3/molecules-30-01659-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/827cbf56d335/molecules-30-01659-sch013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/1f4e53239cff/molecules-30-01659-sch014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/1715bad1dafa/molecules-30-01659-sch015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/8426850ebe9d/molecules-30-01659-sch016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/5ffb8719887b/molecules-30-01659-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/a23eea2e003e/molecules-30-01659-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/a447ab5a5889/molecules-30-01659-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/debb9df7d787/molecules-30-01659-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/3b480d9df84f/molecules-30-01659-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/f031a2fe9f4e/molecules-30-01659-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/d3356883c27a/molecules-30-01659-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/afcfa4d72ca8/molecules-30-01659-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/506299992572/molecules-30-01659-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/2b7e84f71e0a/molecules-30-01659-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/28bd78b0d1a4/molecules-30-01659-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/24cd6d894626/molecules-30-01659-g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/b836a8b31701/molecules-30-01659-g016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/57aabd067145/molecules-30-01659-g017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/633146a09cfe/molecules-30-01659-sch017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/1e0580bdb00a/molecules-30-01659-g018.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/e172f1dea19a/molecules-30-01659-g019.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/fece5e54f1f4/molecules-30-01659-g020.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/12029770/2208e27fe415/molecules-30-01659-sch018.jpg

相似文献

1
Chemistry of 2-(2'-Aminophenyl)benzothiazole Derivatives: Syntheses, Photophysical Properties and Applications.2-(2'-氨基苯基)苯并噻唑衍生物的化学性质:合成、光物理性质及应用
Molecules. 2025 Apr 8;30(8):1659. doi: 10.3390/molecules30081659.
2
Visible-Light Organic Photosensitizers Based on 2-(2-Aminophenyl)benzothiazoles for Photocycloaddition Reactions.基于2-(2-氨基苯基)苯并噻唑的用于光环加成反应的可见光有机光敏剂
Chemistry. 2024 Dec 5;30(68):e202401851. doi: 10.1002/chem.202401851. Epub 2024 Nov 14.
3
Isatin as a 2-aminobenzaldehyde surrogate: transition metal-free efficient synthesis of 2-(2'-aminophenyl)benzothiazole derivatives.异吲哚酮作为2-氨基苯甲醛替代物:无过渡金属高效合成2-(2'-氨基苯基)苯并噻唑衍生物
Org Biomol Chem. 2020 Jun 3. doi: 10.1039/d0ob00888e.
4
Light-emitting self-assembled metallacages.发光自组装金属笼。
Natl Sci Rev. 2021 Mar 17;8(6):nwab045. doi: 10.1093/nsr/nwab045. eCollection 2021 Jun.
5
Luminescent Covalent Organic Frameworks for Biosensing and Bioimaging Applications.用于生物传感和生物成像应用的发光共价有机框架。
Small. 2022 Jan;18(3):e2103516. doi: 10.1002/smll.202103516. Epub 2021 Oct 3.
6
Porpholactone Chemistry: An Emerging Approach to Bioinspired Photosensitizers with Tunable Near-Infrared Photophysical Properties.卟吩内酯化学:一种具有可调近红外光物理性质的仿生光敏剂的新兴方法。
Acc Chem Res. 2019 Sep 17;52(9):2620-2633. doi: 10.1021/acs.accounts.9b00119. Epub 2019 Jul 12.
7
Encapsulation of Luminescent Guests to Construct Luminescent Metal-Organic Frameworks for Chemical Sensing.用于化学传感的发光客体的封装以构建发光金属有机框架
ACS Sens. 2021 Mar 26;6(3):641-658. doi: 10.1021/acssensors.0c02562. Epub 2021 Feb 11.
8
A benzothiazole-rhodol based luminophor: ESIPT-induced AIE and an application for detecting Fe ion.一种基于苯并噻唑-若丹明的发光体:激发态分子内质子转移诱导的聚集诱导发光及其在检测铁离子中的应用。
Spectrochim Acta A Mol Biomol Spectrosc. 2019 Sep 5;220:117114. doi: 10.1016/j.saa.2019.05.019. Epub 2019 May 11.
9
Lanthanide Chemistry: From Coordination in Chemical Complexes Shaping Our Technology to Coordination in Enzymes Shaping Bacterial Metabolism.镧系元素化学:从塑造我们技术的化学配合物中的配位作用到塑造细菌新陈代谢的酶中的配位作用。
Inorg Chem. 2016 Oct 17;55(20):10083-10089. doi: 10.1021/acs.inorgchem.6b00919. Epub 2016 Sep 2.
10
Shining New Light on Biological Systems: Luminescent Transition Metal Complexes for Bioimaging and Biosensing Applications.闪耀生物系统之光:用于生物成像和生物传感应用的发光过渡金属配合物。
Chem Rev. 2024 Aug 14;124(15):8825-9014. doi: 10.1021/acs.chemrev.3c00629. Epub 2024 Jul 25.

本文引用的文献

1
Multitarget Pharmacology of Sulfur-Nitrogen Heterocycles: Anticancer and Antioxidant Perspectives.硫氮杂环化合物的多靶点药理学:抗癌与抗氧化视角
Antioxidants (Basel). 2024 Jul 25;13(8):898. doi: 10.3390/antiox13080898.
2
2-Phenylbenzothiazolyl iridium complexes as inhibitors and probes of amyloid β aggregation.2-苯基苯并噻唑基铱配合物作为淀粉样β聚集的抑制剂和探针。
Dalton Trans. 2024 Aug 27;53(34):14258-14264. doi: 10.1039/d4dt01691b.
3
Visible-Light Organic Photosensitizers Based on 2-(2-Aminophenyl)benzothiazoles for Photocycloaddition Reactions.
基于2-(2-氨基苯基)苯并噻唑的用于光环加成反应的可见光有机光敏剂
Chemistry. 2024 Dec 5;30(68):e202401851. doi: 10.1002/chem.202401851. Epub 2024 Nov 14.
4
A Ratiometric Benzimidazole-Based Fluorescent Probe for The Recognition of Phosgene in Solution and Gaseous Phases.一种基于苯并咪唑的比率型荧光探针,用于识别溶液和气相中的光气。
J Fluoresc. 2024 Jul 15. doi: 10.1007/s10895-024-03847-x.
5
Six-coordinated nickel(II) complexes with benzothiadiazole Schiff-base ligands: synthesis, crystal structure, magnetic and HFEPR study.含苯并噻二唑席夫碱配体的六配位镍(II)配合物:合成、晶体结构、磁性和高频电子顺磁共振研究
Dalton Trans. 2024 May 21;53(20):8835-8842. doi: 10.1039/d4dt01143k.
6
TDDFT Study on the ESIPT Properties of 2-(2'-Hydroxyphenyl)-Benzothiazole and Sensing Mechanism of a Derived Fluorescent Probe for Fluoride Ion.2-(2'-羟基苯基)-苯并噻唑的激发态分子内质子转移性质及一种衍生的氟离子荧光探针传感机制的含时密度泛函理论研究
Molecules. 2024 Mar 29;29(7):1541. doi: 10.3390/molecules29071541.
7
Lanthanide complexes with a new luminescent iminophosphonamide ligand bearing phenylbenzothiazole substituents.镧系元素与一种带有苯基苯并噻唑取代基的新型发光亚氨基膦酰胺配体形成的配合物。
Dalton Trans. 2024 Jan 30;53(5):2181-2192. doi: 10.1039/d3dt03511e.
8
Energy transfer photocatalysis: exciting modes of reactivity.能量转移光催化:激发反应模式
Chem Soc Rev. 2024 Feb 5;53(3):1068-1089. doi: 10.1039/d3cs00190c.
9
The solvent-regulated excited state reaction mechanism of 2-(2'-hydroxyphenyl)benzothiazole aggregates.2-(2'-羟基苯基)苯并噻唑聚集体的溶剂调控激发态反应机理
Photochem Photobiol Sci. 2024 Jan;23(1):65-78. doi: 10.1007/s43630-023-00499-x. Epub 2023 Nov 25.
10
Pd(II)- and Pt(II)-Assisted P-C Activation/Cyclization Reactions with a Luminescent α-Aminophosphine.钯(II)和铂(II)辅助的与发光α-氨基膦的P-C活化/环化反应
Inorg Chem. 2024 Jan 8;63(1):369-380. doi: 10.1021/acs.inorgchem.3c03271. Epub 2023 Nov 21.