• 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]对环芳烷的区域选择性官能团化:近期合成进展与展望

Regioselective Functionalization of [2.2]Paracyclophanes: Recent Synthetic Progress and Perspectives.

作者信息

Hassan Zahid, Spuling Eduard, Knoll Daniel M, Bräse Stefan

机构信息

Institute of Organic Chemistry (IOC), Fritz-Haber-Weg 6, 76131, Karlsruhe, Germany.

3DMM2O-Cluster of Excellence, Institute of Organic Chemistry (IOC), Karlsruhe Institute of Technology (KIT), Germany.

出版信息

Angew Chem Int Ed Engl. 2020 Feb 3;59(6):2156-2170. doi: 10.1002/anie.201904863. Epub 2019 Oct 30.

DOI:10.1002/anie.201904863
PMID:31283092
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7003812/
Abstract

[2.2]Paracyclophane (PCP) is a prevalent scaffold that is widely utilized in asymmetric synthesis, π-stacked polymers, energy materials, and functional parylene coatings that finds broad applications in bio- and materials science. In the last few years, [2.2]paracyclophane chemistry has progressed tremendously, enabling the fine-tuning of its structural and functional properties. This Minireview highlights the most important recent synthetic developments in the selective functionalization of PCP that govern distinct features of planar chirality as well as chiroptical and optoelectronic properties. Special focus is given to the function-inspired design of [2.2]paracyclophane-based π-stacked conjugated materials by transition-metal-catalyzed cross-coupling reactions. Current synthetic challenges, limitations, as well as future research directions and new avenues for advancing cyclophane chemistry are also summarized.

摘要

[2.2]对环芳烷(PCP)是一种普遍存在的骨架,广泛应用于不对称合成、π堆积聚合物、能量材料和功能性聚对二甲苯涂层,在生物和材料科学领域有广泛应用。在过去几年中,[2.2]对环芳烷化学取得了巨大进展,能够对其结构和功能性质进行微调。本综述重点介绍了PCP选择性功能化方面最重要的近期合成进展,这些进展决定了平面手性以及手性光学和光电性质的独特特征。特别关注通过过渡金属催化的交叉偶联反应,基于[2.2]对环芳烷的π堆积共轭材料的功能启发式设计。还总结了当前的合成挑战、局限性以及推进环芳烷化学的未来研究方向和新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/b7bc2f914380/ANIE-59-2156-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/a18c042fc147/ANIE-59-2156-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/c9fedd9706b1/ANIE-59-2156-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/70a01abbd101/ANIE-59-2156-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/c2e054a2e013/ANIE-59-2156-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/13c84c4443cc/ANIE-59-2156-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/33a1f4ac6614/ANIE-59-2156-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/1f1b4765a589/ANIE-59-2156-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/b97a1ae10fca/ANIE-59-2156-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/66c31d0cea60/ANIE-59-2156-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/e982a3cdab21/ANIE-59-2156-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/83da9aef92b1/ANIE-59-2156-g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/76a3ced2978c/ANIE-59-2156-g016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/b1349092acca/ANIE-59-2156-g017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/7c1b126e5a7f/ANIE-59-2156-g018.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/61c934164a96/ANIE-59-2156-g019.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/02294c4d85da/ANIE-59-2156-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/b7bc2f914380/ANIE-59-2156-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/a18c042fc147/ANIE-59-2156-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/c9fedd9706b1/ANIE-59-2156-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/70a01abbd101/ANIE-59-2156-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/c2e054a2e013/ANIE-59-2156-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/13c84c4443cc/ANIE-59-2156-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/33a1f4ac6614/ANIE-59-2156-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/1f1b4765a589/ANIE-59-2156-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/b97a1ae10fca/ANIE-59-2156-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/66c31d0cea60/ANIE-59-2156-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/e982a3cdab21/ANIE-59-2156-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/83da9aef92b1/ANIE-59-2156-g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/76a3ced2978c/ANIE-59-2156-g016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/b1349092acca/ANIE-59-2156-g017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/7c1b126e5a7f/ANIE-59-2156-g018.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/61c934164a96/ANIE-59-2156-g019.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/02294c4d85da/ANIE-59-2156-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/7003812/b7bc2f914380/ANIE-59-2156-g008.jpg

相似文献

1
Regioselective Functionalization of [2.2]Paracyclophanes: Recent Synthetic Progress and Perspectives.[2.2]对环芳烷的区域选择性官能团化:近期合成进展与展望
Angew Chem Int Ed Engl. 2020 Feb 3;59(6):2156-2170. doi: 10.1002/anie.201904863. Epub 2019 Oct 30.
2
Planar chiral [2.2]paracyclophanes: from synthetic curiosity to applications in asymmetric synthesis and materials.平面手性[2.2]对环芳烷:从合成好奇心到不对称合成和材料应用。
Chem Soc Rev. 2018 Sep 17;47(18):6947-6963. doi: 10.1039/c7cs00803a.
3
Design Strategies for Structurally Controlled Polymer Surfaces via Cyclophane-Based CVD Polymerization and Post-CVD Fabrication.通过基于环芳烷的化学气相沉积聚合和化学气相沉积后加工制备结构可控聚合物表面的设计策略
Adv Mater. 2022 Sep;34(37):e2201761. doi: 10.1002/adma.202201761. Epub 2022 Aug 9.
4
Macrocyclic Oligothiophene with Stereogenic [2.2]Paracyclophane Scaffolds: Chiroptical Properties from π-Transannular Interactions.具有手性[2.2]对环芳烷骨架的大环低聚噻吩:π-跨环相互作用产生的手性光学性质
Chemistry. 2017 Mar 8;23(14):3267-3271. doi: 10.1002/chem.201605842. Epub 2017 Feb 16.
5
Synthesis of Two Novel Optically Active #-Shaped Cyclic Tetramers Based on Planar Chiral [2.2]Paracyclophanes.基于平面手性[2.2]对环芳烷合成两种新型光学活性#形环状四聚体。
Chemistry. 2023 Mar 28;29(18):e202203533. doi: 10.1002/chem.202203533. Epub 2023 Feb 21.
6
Control of Circularly Polarized Luminescence by Orientation of Stacked π-Electron Systems.通过堆叠π电子系统的取向控制圆偏振发光
Chem Asian J. 2019 May 15;14(10):1681-1685. doi: 10.1002/asia.201801741. Epub 2019 Jan 25.
7
3D Coumarin Systems Based on [2.2]Paracyclophane: Synthesis, Spectroscopic Characterization, and Chiroptical Properties.基于[2.2]对环芳烷的3D香豆素体系:合成、光谱表征及手性光学性质
J Org Chem. 2019 Jan 18;84(2):888-899. doi: 10.1021/acs.joc.8b02773. Epub 2019 Jan 9.
8
Synthesis of Planar Chiral Ferrocenes via Transition-Metal-Catalyzed Direct C-H Bond Functionalization.通过过渡金属催化的直接 C-H 键功能化合成平面手性二茂铁。
Acc Chem Res. 2017 Feb 21;50(2):351-365. doi: 10.1021/acs.accounts.6b00573. Epub 2017 Jan 25.
9
Intense Molar Circular Dichroism in Fully Conjugated All-Carbon Macrocyclic 1,3-Butadiyne Linked pseudo-meta [2.2]Paracyclophanes.全共轭全碳大环1,3 - 丁二炔连接的准间位[2.2]对环芳烷中的强摩尔圆二色性
Chemistry. 2022 Sep 22;28(53):e202201764. doi: 10.1002/chem.202201764. Epub 2022 Aug 3.
10
Coordination-Driven Syntheses of Compact Supramolecular Metallacycles toward Extended Metallo-organic Stacked Supramolecular Assemblies.基于配位驱动的超分子金属环的紧密组装来构筑延展的金属有机堆积超分子组装体。
Acc Chem Res. 2017 Apr 18;50(4):885-894. doi: 10.1021/acs.accounts.6b00624. Epub 2017 Mar 6.

引用本文的文献

1
Synthesis of optically active folded cyclic dimers and trimers.光学活性折叠环状二聚体和三聚体的合成。
Beilstein J Org Chem. 2025 Aug 11;21:1603-1612. doi: 10.3762/bjoc.21.124. eCollection 2025.
2
Isothiourea-Catalysed Acylative Kinetic and Dynamic Kinetic Resolution of Planar Chiral Paracyclophanols.异硫脲催化的平面手性对环芳醇的酰基化动力学拆分和动态动力学拆分
Angew Chem Int Ed Engl. 2025 Jul 28;64(31):e202507126. doi: 10.1002/anie.202507126. Epub 2025 Jun 23.
3
Construction of planar chiral [2,2]paracyclophanes via photoinduced cobalt-catalyzed desymmetric addition.

本文引用的文献

1
Turn on of sky-blue thermally activated delayed fluorescence and circularly polarized luminescence (CPL) increased torsion by a bulky carbazolophane donor.通过一个庞大的咔唑环戊烷供体开启天蓝色热激活延迟荧光和圆偏振发光(CPL)可增加扭转。
Chem Sci. 2019 May 29;10(27):6689-6696. doi: 10.1039/c9sc01821b. eCollection 2019 Jul 21.
2
Rational design and implementation of a cucurbit[8]uril-based indicator-displacement assay for application in blood serum.用于血清检测的基于葫芦[8]脲的指示剂置换分析方法的合理设计与实施。
Chem Sci. 2019 Jun 4;10(27):6584-6593. doi: 10.1039/c9sc00705a. eCollection 2019 Jul 21.
3
Indeno[1,2-b]fluorene-Based [2,2]Cyclophanes with 4n/4n and 4n/[4n+2] π Electrons: Syntheses, Structural Analyses, and Excitonic Coupling Properties.
通过光诱导钴催化的去对称加成反应构建平面手性[2,2]对环芳烷
Nat Commun. 2025 Apr 29;16(1):4012. doi: 10.1038/s41467-025-59089-3.
4
Polyaromatic Cyclophanes Design and their Related Optical Properties.聚芳环环蕃的设计及其相关光学性质。
ChemistryOpen. 2025 Apr;14(4):e202400207. doi: 10.1002/open.202400207. Epub 2024 Dec 4.
5
A New Class of Chiral Polyethers and Polyesters Based on the [2.2]Paracyclophane Scaffold.基于[2.2]对环芳烷骨架的一类新型手性聚醚和聚酯。
Polymers (Basel). 2024 Jun 5;16(11):1603. doi: 10.3390/polym16111603.
6
Rhodium(II)-Catalyzed Asymmetric Cyclopropanation and Desymmetrization of [2.2]Paracyclophanes.铑(II)催化的[2.2]对环芳烷的不对称环丙烷化反应和去对称化反应
ACS Catal. 2024 Apr 11;14(9):6423-6431. doi: 10.1021/acscatal.4c01292. eCollection 2024 May 3.
7
Organocatalytic desymmetrization provides access to planar chiral [2.2]paracyclophanes.有机催化去对称化反应为合成平面手性[2.2]对环芳烷提供了途径。
Nat Commun. 2024 Apr 10;15(1):3090. doi: 10.1038/s41467-024-47407-0.
8
Synthesis of Mono-, Di-, Tri-, and Tetra-cationic Pyridinium and Vinylpyridinium Modified [2.2]Paracyclophanes: Modular Receptors for Supramolecular Systems.单阳离子、双阳离子、三阳离子和四阳离子吡啶鎓及乙烯基吡啶鎓修饰的[2.2]对环芳烷的合成:超分子体系的模块化受体
ChemistryOpen. 2024 Aug;13(8):e202400024. doi: 10.1002/open.202400024. Epub 2024 Mar 12.
9
Functionalized [2.2]Paracyclophanedienes as Monomers for Poly(-phenylenevinylene)s.功能化的[2.2]对环芳二烯作为聚对苯撑乙烯撑的单体
ACS Macro Lett. 2024 Jan 8;13(2):112-117. doi: 10.1021/acsmacrolett.3c00714.
10
Aggregation-induced emission from optically active X-shaped molecules based on planar chiral [2.2]paracyclophane.基于平面手性[2.2]对环芳烷的光学活性X形分子的聚集诱导发光。
Sci Rep. 2023 Dec 19;13(1):22647. doi: 10.1038/s41598-023-49120-2.
基于茚并[1,2-b]芴的具有4n/4n和4n/[4n+2]π电子的[2,2]环芳:合成、结构分析及激子耦合性质
Angew Chem Int Ed Engl. 2019 Jul 22;58(30):10158-10162. doi: 10.1002/anie.201903561. Epub 2019 Jun 13.
4
Poly(arylenevinylene)s through Ring-Opening Metathesis Polymerization of an Unsymmetrical Donor-Acceptor Cyclophane.通过不对称供体-受体环芳烷的开环易位聚合制备聚(亚芳基乙烯撑)
Angew Chem Int Ed Engl. 2019 Jul 8;58(28):9527-9532. doi: 10.1002/anie.201905137. Epub 2019 Jun 6.
5
Highly Enantioselective Asymmetric Transfer Hydrogenation: A Practical and Scalable Method To Efficiently Access Planar Chiral [2.2]Paracyclophanes.高度对映选择性不对称转移氢化:一种高效获取平面手性[2.2]对环芳烷的实用且可扩展的方法。
J Org Chem. 2019 May 3;84(9):5369-5382. doi: 10.1021/acs.joc.9b00372. Epub 2019 Mar 28.
6
Mechanical Stabilization of Helical Chirality in a Macrocyclic Oligothiophene.大环寡聚噻吩中环螺旋手性的机械稳定。
J Am Chem Soc. 2019 Feb 6;141(5):2104-2110. doi: 10.1021/jacs.8b11797. Epub 2019 Jan 25.
7
Templated nanofiber synthesis via chemical vapor polymerization into liquid crystalline films.通过化学气相聚合将模板纳米纤维合成到液晶膜中。
Science. 2018 Nov 16;362(6416):804-808. doi: 10.1126/science.aar8449.
8
Planar chiral [2.2]paracyclophanes: from synthetic curiosity to applications in asymmetric synthesis and materials.平面手性[2.2]对环芳烷:从合成好奇心到不对称合成和材料应用。
Chem Soc Rev. 2018 Sep 17;47(18):6947-6963. doi: 10.1039/c7cs00803a.
9
(Deep) blue through-space conjugated TADF emitters based on [2.2]paracyclophanes.基于[2.2]对环芳烷的(深)蓝色远程共轭 TADF 发射器。
Chem Commun (Camb). 2018 Aug 16;54(67):9278-9281. doi: 10.1039/c8cc04594a.
10
Effect of multi-armed triphenylamine-based hole transporting materials for high performance perovskite solar cells.用于高性能钙钛矿太阳能电池的多臂三苯胺基空穴传输材料的效应
Chem Sci. 2016 Aug 1;7(8):5517-5522. doi: 10.1039/c6sc00876c. Epub 2016 May 17.