• 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

基于邻醌型和二茂铁型氧化还原活性螯合配体的具有扩展氧化还原性质的杂配金属配合物。

Heteroligand Metal Complexes with Extended Redox Properties Based on Redox-Active Chelating Ligands of o-Quinone Type and Ferrocene.

机构信息

G.A. Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences, 603950 Nizhny Novgorod, Russia.

出版信息

Molecules. 2022 Jun 19;27(12):3928. doi: 10.3390/molecules27123928.

DOI:10.3390/molecules27123928
PMID:35745052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9230781/
Abstract

A combination of different types of redox-active systems in one molecule makes it possible to create coordination compounds with extended redox abilities, combining molecular and electronic structures determined by the features of intra- and intermolecular interactions between such redox-active centres. This review summarizes and analyses information from the literature, published mainly from 2000 to the present, on the methods of preparation, the molecular and electronic structure of mixed-ligand coordination compounds based on redox-active ligands of the o-benzoquinone type and ferrocenes, ferrocene-containing ligands, the features of their redox properties, and some chemical behaviour.

摘要

一种分子中结合不同类型的氧化还原活性体系,使得有可能创造具有扩展氧化还原能力的配位化合物,将分子和电子结构结合起来,由这种氧化还原活性中心之间的分子内和分子间相互作用的特征决定。这篇综述总结和分析了文献中的信息,这些信息主要发表于 2000 年至今,内容涉及基于邻苯醌型和二茂铁型氧化还原活性配体、二茂铁配体的混合配体配位化合物的制备方法、分子和电子结构、氧化还原性质的特点以及一些化学行为。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/9825e0347c5e/molecules-27-03928-sch033.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/4bedd378744c/molecules-27-03928-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/987772c4a10c/molecules-27-03928-sch004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/c9b18a9cd92a/molecules-27-03928-sch006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/5e35cfc831f4/molecules-27-03928-sch008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/150e7ea38bb9/molecules-27-03928-sch010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/cc9b0adaf8dd/molecules-27-03928-sch012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/00d217ee8969/molecules-27-03928-sch014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/47d7e435f388/molecules-27-03928-sch016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/d28dadb393a8/molecules-27-03928-sch017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/b61f6d1e1e8d/molecules-27-03928-sch018.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/2b1e796f9bdf/molecules-27-03928-sch019.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/2d73dadeec77/molecules-27-03928-sch020.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/bf7fb207de23/molecules-27-03928-sch021.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/fe793b7e3c0c/molecules-27-03928-sch022.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/3020128d4b39/molecules-27-03928-sch023.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/484436642ad6/molecules-27-03928-sch024.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/e4949af5e62e/molecules-27-03928-sch025.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/b219217c7d63/molecules-27-03928-sch026.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/2162fd9ec876/molecules-27-03928-sch027.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/7d38db25a177/molecules-27-03928-sch028.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/1c90609d245f/molecules-27-03928-sch029.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/a30815ec98a0/molecules-27-03928-sch030.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/2555d245a168/molecules-27-03928-sch031.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/d5b0e274a4fe/molecules-27-03928-sch032.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/9825e0347c5e/molecules-27-03928-sch033.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/4bedd378744c/molecules-27-03928-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/987772c4a10c/molecules-27-03928-sch004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/c9b18a9cd92a/molecules-27-03928-sch006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/5e35cfc831f4/molecules-27-03928-sch008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/150e7ea38bb9/molecules-27-03928-sch010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/cc9b0adaf8dd/molecules-27-03928-sch012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/00d217ee8969/molecules-27-03928-sch014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/47d7e435f388/molecules-27-03928-sch016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/d28dadb393a8/molecules-27-03928-sch017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/b61f6d1e1e8d/molecules-27-03928-sch018.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/2b1e796f9bdf/molecules-27-03928-sch019.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/2d73dadeec77/molecules-27-03928-sch020.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/bf7fb207de23/molecules-27-03928-sch021.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/fe793b7e3c0c/molecules-27-03928-sch022.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/3020128d4b39/molecules-27-03928-sch023.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/484436642ad6/molecules-27-03928-sch024.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/e4949af5e62e/molecules-27-03928-sch025.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/b219217c7d63/molecules-27-03928-sch026.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/2162fd9ec876/molecules-27-03928-sch027.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/7d38db25a177/molecules-27-03928-sch028.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/1c90609d245f/molecules-27-03928-sch029.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/a30815ec98a0/molecules-27-03928-sch030.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/2555d245a168/molecules-27-03928-sch031.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/d5b0e274a4fe/molecules-27-03928-sch032.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ff/9230781/9825e0347c5e/molecules-27-03928-sch033.jpg

相似文献

1
Heteroligand Metal Complexes with Extended Redox Properties Based on Redox-Active Chelating Ligands of o-Quinone Type and Ferrocene.基于邻醌型和二茂铁型氧化还原活性螯合配体的具有扩展氧化还原性质的杂配金属配合物。
Molecules. 2022 Jun 19;27(12):3928. doi: 10.3390/molecules27123928.
2
Reactions of aromatic N-heterocycles with d0fn-metal alkyl complexes supported by chelating diamide ligands.含螯合二酰胺配体的 d0fn-金属烷基配合物与芳香族 N-杂环的反应。
Acc Chem Res. 2010 Oct 19;43(10):1352-63. doi: 10.1021/ar1000605.
3
Three-way cooperativity in d8 metal complexes with ligands displaying chemical and redox non-innocence.具有化学和氧化还原非惰性配体的d8金属配合物中的三方协同作用。
Chemistry. 2014 Nov 10;20(46):15178-87. doi: 10.1002/chem.201403276. Epub 2014 Sep 22.
4
Ferrocene-Containing Tin(IV) Complexes Based on -Benzoquinone and -Iminobenzoquinone Ligands. Synthesis, Molecular Structure, and Electrochemical Properties.基于对苯醌和亚胺基对苯醌配体的含二茂铁锡(IV)配合物。合成、分子结构及电化学性质
Inorg Chem. 2020 May 18;59(10):6774-6784. doi: 10.1021/acs.inorgchem.9b03757. Epub 2020 Apr 27.
5
Redox-Triggered Disassembly of Nanosized Liposomes Containing Ferrocene-Appended Amphiphiles.含二茂铁封端两亲分子的纳米脂质体的氧化还原触发解组装。
Langmuir. 2019 Apr 23;35(16):5608-5616. doi: 10.1021/acs.langmuir.8b04267. Epub 2019 Apr 12.
6
Utilization of phosphinoamide ligands in homobimetallic Fe and Mn complexes: the effect of disparate coordination environments on metal-metal interactions and magnetic and redox properties.膦酰胺配体在同双核 Fe 和 Mn 配合物中的应用:不同配位环境对金属-金属相互作用以及磁和氧化还原性质的影响。
Inorg Chem. 2012 Aug 6;51(15):8225-40. doi: 10.1021/ic300776y. Epub 2012 Jul 17.
7
Ferrocene-o-benzosemiquinonato tin(IV) electron-transfer complexes.二茂铁邻苯醌亚锡(IV)电子转移配合物。
Inorg Chem. 2013 May 6;52(9):5284-9. doi: 10.1021/ic400713p. Epub 2013 Apr 8.
8
The Renaissance of Ferrocene-Based Electrocatalysts: Properties, Synthesis Strategies, and Applications.基于二茂铁的电催化剂的复兴:性质、合成策略及应用。
Top Curr Chem (Cham). 2023 Nov 1;381(6):32. doi: 10.1007/s41061-023-00441-w.
9
Biopyrrin Pigments: From Heme Metabolites to Redox-Active Ligands and Luminescent Radicals.双吡咯色素:从血红素代谢产物到氧化还原活性配体和发光自由基
Acc Chem Res. 2021 Dec 21;54(24):4584-4594. doi: 10.1021/acs.accounts.1c00613. Epub 2021 Dec 6.
10
Temperature-independent catalytic two-electron reduction of dioxygen by ferrocenes with a copper(II) tris[2-(2-pyridyl)ethyl]amine catalyst in the presence of perchloric acid.在高氯酸存在下,用铜(II)三[2-(2-吡啶基)乙基]胺催化剂催化二茂铁进行与温度无关的两电子还原氧气。
J Am Chem Soc. 2013 Feb 20;135(7):2825-34. doi: 10.1021/ja312523u. Epub 2013 Feb 8.

引用本文的文献

1
Multi-Ferrocene-Based Ligands: From Design to Applications.基于多二茂铁的配体:从设计到应用
Chem Rev. 2025 Mar 26;125(6):3007-3058. doi: 10.1021/acs.chemrev.4c00295. Epub 2025 Mar 17.
2
Recent Catalytic Applications of Ferrocene and Ferrocenium Cations in the Syntheses of Organic Compounds.二茂铁和二茂铁阳离子在有机化合物合成中的最新催化应用
Molecules. 2024 Nov 23;29(23):5544. doi: 10.3390/molecules29235544.
3
Low-Coordinate Mixed Ligand NacNac Complexes of Rare Earth Metals.低配位混合配体 NacNac 稀土金属配合物。

本文引用的文献

1
Forever young: the first seventy years of ferrocene.永远年轻:二茂铁的七十年。
Dalton Trans. 2022 May 31;51(21):8085-8102. doi: 10.1039/d2dt00903j.
2
Dinickel Active Sites Supported by Redox-Active Ligands.含氧化还原活性配体的二镍活性中心。
Acc Chem Res. 2021 Oct 5;54(19):3710-3719. doi: 10.1021/acs.accounts.1c00424. Epub 2021 Sep 26.
3
Co(II) complexes of curcumin and a ferrocene-based curcuminoid: a study on photo-induced antitumor activity.姜黄素与一种基于二茂铁的姜黄素类似物的钴(II)配合物:光诱导抗肿瘤活性研究
Molecules. 2023 Feb 20;28(4):1994. doi: 10.3390/molecules28041994.
J Biol Inorg Chem. 2021 Dec;26(8):881-893. doi: 10.1007/s00775-021-01899-z. Epub 2021 Sep 22.
4
Controlling Radical-Type Single-Electron Elementary Steps in Catalysis with Redox-Active Ligands and Substrates.利用氧化还原活性配体和底物控制催化中自由基型单电子基本步骤
JACS Au. 2021 Jul 6;1(8):1101-1115. doi: 10.1021/jacsau.1c00224. eCollection 2021 Aug 23.
5
Nature of Asymmetric Electron Transfer in the Symmetric Pathways of Photosystem I.光系统I对称途径中不对称电子转移的本质
J Phys Chem B. 2021 Mar 25;125(11):2879-2885. doi: 10.1021/acs.jpcb.0c10885. Epub 2021 Mar 10.
6
Strategies and mechanisms of metal-ligand cooperativity in first-row transition metal complex catalysts.第一行过渡金属配合物催化剂中金属-配体协同作用的策略与机制
Chem Soc Rev. 2020 Dec 21;49(24):8933-8987. doi: 10.1039/d0cs00509f. Epub 2020 Nov 9.
7
Recent developments in the synthesis and applications of chiral ferrocene ligands and organocatalysts in asymmetric catalysis.手性二茂铁配体和有机催化剂在不对称催化中合成与应用的最新进展。
Org Biomol Chem. 2020 Dec 7;18(46):9329-9370. doi: 10.1039/d0ob01933j.
8
Assigning Ligand Redox Levels in Complexes of 2-Aminophenolates: Structural Signatures.确定2-氨基酚盐配合物中的配体氧化还原水平:结构特征
Inorg Chem. 2020 Sep 21;59(18):12961-12977. doi: 10.1021/acs.inorgchem.0c00240. Epub 2020 Sep 3.
9
Multifaceted aspects of charge transfer.电荷转移的多方面特性。
Phys Chem Chem Phys. 2020 Oct 14;22(38):21583-21629. doi: 10.1039/d0cp01556c. Epub 2020 Aug 12.
10
Copper catalysis with redox-active ligands.铜与氧化还原活性配体的催化作用。
Beilstein J Org Chem. 2020 Apr 24;16:858-870. doi: 10.3762/bjoc.16.77. eCollection 2020.