• 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

基于四嗪的连接体作为金属有机框架点击功能化的固有标记替代物。

Tetrazine-based linkers as intrinsically tagged alternatives for click functionalization of metal-organic frameworks.

作者信息

Gómez-Tenés Guillermo, Gimeno-Fonquernie Pol, Misturini Alechania, Chinchilla-Garzón Clara, Carratalá Víctor, Cisneros Larisha, Martí-Gastaldo Carlos

机构信息

Functional Inorganic Materials Team, Instituto de Ciencia Molecular (ICMol), Universitat de València, Paterna 46980, Spain.

出版信息

Chem Commun (Camb). 2024 Nov 5;60(89):12977-12985. doi: 10.1039/d4cc03456b.

DOI:10.1039/d4cc03456b
PMID:39431569
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12164735/
Abstract

Reticular chemistry has in the post-synthetic modification (PSM) of frameworks one of the most versatile tools to adapt the systems' physicochemical properties to the specific requirements which are imposed by their application in different contexts. We can safely say that PSM methodologies in all their variants are currently one of the main resources that reticular chemists turn to when they need to diversify a framework compositionally. Practically all these modifications require the integration of functional groups appended to the organic linkers in the framework, either by direct synthesis or by post-synthetic exchange. The reactivity of these tags allows, at a subsequent stage, covalent modification of the framework under conditions that ideally respect its structural integrity. In this perspective article we introduce the use of tetrazine-based linkers as intrinsically tagged alternatives to integrate PSM with click chemistry reactivity. This strategy is ideally suited to molecular frameworks, as it combines very mild modification conditions with direct control over the organisation of built-in appendices and the acknowledged potential of click chemistry to build framework libraries.

摘要

网状化学在框架的合成后修饰(PSM)中是一种极为通用的工具,可使体系的物理化学性质适应于因其在不同情境中的应用而产生的特定要求。我们可以确切地说,目前,各种变体的PSM方法是网状化学家在需要从组成上使框架多样化时所依赖的主要资源之一。实际上,所有这些修饰都需要通过直接合成或合成后交换,将连接到框架中有机连接体上的官能团整合进去。这些标签的反应活性使得在后续阶段能够在理想情况下尊重其结构完整性的条件下对框架进行共价修饰。在这篇观点文章中,我们介绍使用基于四嗪的连接体作为具有内在标签的替代物,将PSM与点击化学反应性相结合。这种策略非常适合分子框架,因为它将非常温和的修饰条件与对内置附件组织的直接控制以及点击化学在构建框架库方面公认的潜力结合在一起。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0337/12164735/523f7dc41485/d4cc03456b-p4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0337/12164735/f92d18682190/d4cc03456b-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0337/12164735/b6af158098c5/d4cc03456b-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0337/12164735/192a52d8b04a/d4cc03456b-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0337/12164735/b845d7f57db9/d4cc03456b-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0337/12164735/0ae471c62e77/d4cc03456b-p1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0337/12164735/aee321aad3c5/d4cc03456b-p2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0337/12164735/d0dd18a2d949/d4cc03456b-p3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0337/12164735/523f7dc41485/d4cc03456b-p4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0337/12164735/f92d18682190/d4cc03456b-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0337/12164735/b6af158098c5/d4cc03456b-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0337/12164735/192a52d8b04a/d4cc03456b-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0337/12164735/b845d7f57db9/d4cc03456b-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0337/12164735/0ae471c62e77/d4cc03456b-p1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0337/12164735/aee321aad3c5/d4cc03456b-p2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0337/12164735/d0dd18a2d949/d4cc03456b-p3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0337/12164735/523f7dc41485/d4cc03456b-p4.jpg

相似文献

1
Tetrazine-based linkers as intrinsically tagged alternatives for click functionalization of metal-organic frameworks.基于四嗪的连接体作为金属有机框架点击功能化的固有标记替代物。
Chem Commun (Camb). 2024 Nov 5;60(89):12977-12985. doi: 10.1039/d4cc03456b.
2
Tetrazine Linkers as Plug-and-Play Tags for General Metal-Organic Framework Functionalization and C Conjugation.四嗪连接体作为通用金属有机框架功能化和碳共轭的即插即用标签
Angew Chem Int Ed Engl. 2022 Oct 10;61(41):e202208139. doi: 10.1002/anie.202208139. Epub 2022 Sep 5.
3
Reversible Postsynthetic Modification in a Metal-Organic Framework.金属有机框架中的可逆合成后修饰
Angew Chem Int Ed Engl. 2024 Feb 26;63(9):e202317062. doi: 10.1002/anie.202317062. Epub 2024 Jan 18.
4
Covalent Metal-Organic Frameworks: Fusion of Covalent Organic Frameworks and Metal-Organic Frameworks.共价金属有机框架:共价有机框架与金属有机框架的融合
Acc Chem Res. 2025 Mar 4;58(5):746-761. doi: 10.1021/acs.accounts.4c00774. Epub 2025 Feb 21.
5
Amine-Tagged Fragmented Ligand Installation for Covalent Modification of MOF-74.用于MOF-74共价修饰的胺标记片段配体安装
Angew Chem Int Ed Engl. 2021 Apr 19;60(17):9296-9300. doi: 10.1002/anie.202100456. Epub 2021 Mar 5.
6
Tandem postsynthetic modification of metal-organic frameworks using an inverse-electron-demand Diels-Alder reaction.利用逆电子需求 Diels-Alder 反应对金属有机骨架进行串联后合成修饰。
Inorg Chem. 2011 Nov 7;50(21):10534-6. doi: 10.1021/ic2017598. Epub 2011 Oct 10.
7
Postsynthetic Modification of Metal-Organic Layers.金属有机层的合成后修饰
Acc Chem Res. 2025 Mar 18;58(6):812-823. doi: 10.1021/acs.accounts.4c00726. Epub 2025 Mar 6.
8
Tailoring the Pore Surface of 3D Covalent Organic Frameworks via Post-Synthetic Click Chemistry.通过后合成点击化学定制三维共价有机框架的孔表面
Angew Chem Int Ed Engl. 2022 Jan 10;61(2):e202113852. doi: 10.1002/anie.202113852. Epub 2021 Nov 29.
9
Postsynthetic Tuning of Metal-Organic Frameworks for Targeted Applications.后合成调谐金属-有机骨架用于靶向应用。
Acc Chem Res. 2017 Apr 18;50(4):805-813. doi: 10.1021/acs.accounts.6b00577. Epub 2017 Feb 8.
10
Post-synthetic modification of covalent organic frameworks.共价有机框架的合成后修饰
Chem Soc Rev. 2019 Jul 15;48(14):3903-3945. doi: 10.1039/c8cs00978c.

引用本文的文献

1
Pore Size Engineering of MOFs by Pore Edge Reaction: Tetrazine Click and Hydrogen Adsorption in Theory and Experiment.通过孔边缘反应对金属有机框架进行孔径工程:四嗪点击反应与氢气吸附的理论与实验研究
Chem Mater. 2025 Jul 2;37(14):5206-5216. doi: 10.1021/acs.chemmater.5c00914. eCollection 2025 Jul 22.

本文引用的文献

1
Structural Transformations of Metal-Organic Cages through Tetrazine-Alkene Reactivity.通过四嗪-烯烃反应实现金属有机笼的结构转变
J Am Chem Soc. 2024 Sep 5;146(41):28233-41. doi: 10.1021/jacs.4c08591.
2
Covalent Modification by Click Mechanochemistry: Systematic Installation of Pendant OH Groups in a MOF for Rigidity Control and Luminescence-Based Water Detection.点击机械化学的共价修饰:在 MOF 中系统地安装悬垂 OH 基团以控制刚性和基于发光的水检测。
ACS Appl Mater Interfaces. 2023 May 31;15(21):25661-25670. doi: 10.1021/acsami.3c00788. Epub 2023 May 19.
3
A Special Virtual Issue Celebrating the 2022 Nobel Prize in Chemistry for the Development of Click Chemistry and Bioorthogonal Chemistry.
一期特别虚拟专刊,以庆祝因点击化学和生物正交化学的发展而荣获2022年诺贝尔化学奖。
ACS Cent Sci. 2022 Dec 5;9(4):558-559. doi: 10.1021/acscentsci.2c01430. eCollection 2023 Apr 26.
4
Tetrazine Linkers as Plug-and-Play Tags for General Metal-Organic Framework Functionalization and C Conjugation.四嗪连接体作为通用金属有机框架功能化和碳共轭的即插即用标签
Angew Chem Int Ed Engl. 2022 Oct 10;61(41):e202208139. doi: 10.1002/anie.202208139. Epub 2022 Sep 5.
5
Uncovering the Key Role of Distortion in Bioorthogonal Tetrazine Tools That Defy the Reactivity/Stability Trade-Off.揭示扭曲在生物正交四嗪工具中关键作用,这些工具打破了反应性/稳定性的权衡。
J Am Chem Soc. 2022 May 11;144(18):8171-8177. doi: 10.1021/jacs.2c01056. Epub 2022 May 2.
6
Clip to Click: Controlling Inverse Electron-Demand Diels-Alder Reactions with Macrocyclic Tetrazines.从夹子到点击反应:利用大环四嗪控制逆电子需求的狄尔斯-阿尔德反应
Org Lett. 2022 May 6;24(17):3223-3226. doi: 10.1021/acs.orglett.2c01010. Epub 2022 Apr 21.
7
Effect of Linker Distribution in the Photocatalytic Activity of Multivariate Mesoporous Crystals.多元介孔晶体中连接子分布对光催化活性的影响。
J Am Chem Soc. 2021 Feb 3;143(4):1798-1806. doi: 10.1021/jacs.0c09015. Epub 2021 Jan 12.
8
Crystal engineering of a rectangular coordination network to enable xylenes selectivity over ethylbenzene.用于实现二甲苯相对于乙苯的选择性的矩形配位网络的晶体工程。
Chem Sci. 2020 Jun 16;11(26):6889-6895. doi: 10.1039/d0sc02123g. eCollection 2020 Jul 14.
9
A Highly Water-Stable -Carborane-Based Copper Metal-Organic Framework for Efficient High-Temperature Butanol Separation.一种高水稳定性的基于-carborane 的铜金属有机骨架,用于高效高温丁醇分离。
J Am Chem Soc. 2020 May 6;142(18):8299-8311. doi: 10.1021/jacs.0c01008. Epub 2020 Apr 27.
10
TetrazineBox: A Structurally Transformative Toolbox.四嗪盒:结构转化工具盒。
J Am Chem Soc. 2020 Mar 18;142(11):5419-5428. doi: 10.1021/jacs.0c01114. Epub 2020 Mar 5.