• 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

受限空间中的过渡金属催化作用。

Transition metal catalysis in confined spaces.

机构信息

Homogeneous, Supramolecular and Bio-inspired Catalysis Group, Van 't Hoff Institute for Molecular Science (HIMS), University of Amsterdam (UvA), Science Park 904, 1098 XH Amsterdam, The Netherlands.

出版信息

Chem Soc Rev. 2015 Jan 21;44(2):433-48. doi: 10.1039/c4cs00192c.

DOI:10.1039/c4cs00192c
PMID:25340992
Abstract

Transition metal catalysis plays an important role in both industry and in academia where selectivity, activity and stability are crucial parameters to control. Next to changing the structure of the ligand, introducing a confined space as a second coordination sphere around a metal catalyst has recently been shown to be a viable method to induce new selectivity and activity in transition metal catalysis. In this review we focus on supramolecular strategies to encapsulate transition metal complexes with the aim of controlling the selectivity via the second coordination sphere. As we will discuss, catalyst confinement can result in selective processes that are impossible or difficult to achieve by traditional methods. We will describe the template-ligand approach as well as the host-guest approach to arrive at such supramolecular systems and discuss how the performance of the catalyst is enhanced by confining it in a molecular container.

摘要

过渡金属催化在工业和学术界都起着重要作用,其中选择性、活性和稳定性是控制的关键参数。除了改变配体的结构外,最近还表明,在金属催化剂周围引入受限空间作为第二配位球,是诱导过渡金属催化中产生新选择性和活性的一种可行方法。在这篇综述中,我们专注于超分子策略来封装过渡金属配合物,旨在通过第二配位球控制选择性。正如我们将讨论的那样,催化剂的限制可以导致通过传统方法不可能或难以实现的选择性过程。我们将描述模板配体方法以及主客体方法来获得这样的超分子体系,并讨论将催化剂限制在分子容器中如何增强其性能。

相似文献

1
Transition metal catalysis in confined spaces.受限空间中的过渡金属催化作用。
Chem Soc Rev. 2015 Jan 21;44(2):433-48. doi: 10.1039/c4cs00192c.
2
Supramolecular control of transition metal complexes in water by a hydrophobic cavity: a bio-inspired strategy.疏水腔对水中过渡金属配合物的超分子控制:一种受生物启发的策略。
Org Biomol Chem. 2015 Mar 14;13(10):2849-65. doi: 10.1039/c4ob02511c.
3
Transition Metal Catalysis Controlled by Hydrogen Bonding in the Second Coordination Sphere.氢键在第二配位球中控制的过渡金属催化作用。
Chem Rev. 2022 Jul 27;122(14):12308-12369. doi: 10.1021/acs.chemrev.1c00862. Epub 2022 May 20.
4
Asymmetric catalysis mediated by the ligand sphere of octahedral chiral-at-metal complexes.由八面体手性金属配合物的配体场介导的不对称催化。
Angew Chem Int Ed Engl. 2014 Oct 6;53(41):10868-74. doi: 10.1002/anie.201404305. Epub 2014 Aug 25.
5
Metal-ligand binding interactions in rhodium/palladium-catalyzed synthesis of dihydroquinolines.铑/钯催化合成二氢喹啉中的金属-配体结合相互作用。
J Org Chem. 2014 Dec 19;79(24):12159-76. doi: 10.1021/jo502074s. Epub 2014 Nov 7.
6
Remote supramolecular control of catalyst selectivity in the hydroformylation of alkenes.烯烃氢甲酰化反应中催化剂选择性的远程超分子控制
Angew Chem Int Ed Engl. 2011 Jan 10;50(2):396-400. doi: 10.1002/anie.201005173.
7
Mono(NCN-pincer palladium)-metalloporphyrin catalysts: evidence for supramolecular bimetallic catalysis.单核(NCN-钳钯)-金属卟啉催化剂:超分子双金属催化的证据。
Dalton Trans. 2010 Jul 21;39(27):6198-216. doi: 10.1039/b925236n. Epub 2010 Jun 2.
8
New carbon- and sulfur-based ligands in catalysis.催化领域中新型的碳基和硫基配体。
Chimia (Aarau). 2011;65(10):806-12. doi: 10.2533/chimia.2011.806.
9
Template-free multicomponent coordination-driven self-assembly of Pd(II)/Pt(II) molecular cages.无模板的多组分配位驱动自组装 Pd(II)/Pt(II) 分子笼。
Chem Commun (Camb). 2014 Mar 4;50(18):2239-48. doi: 10.1039/c3cc49192g. Epub 2014 Jan 27.
10
Application of Coordination Compounds with Transition Metal Ions in the Chemical Industry-A Review.过渡金属离子配合物在化学工业中的应用综述。
Int J Mol Sci. 2020 Jul 30;21(15):5443. doi: 10.3390/ijms21155443.

引用本文的文献

1
Carboxylato-prism[6]arene as a supramolecular catalyst in water: exploiting its deep hydrophobic cavity for green oxidation of aromatic amines.羧基化棱柱[6]芳烃作为水中的超分子催化剂:利用其深疏水腔实现芳香胺的绿色氧化
Chem Sci. 2025 Aug 29. doi: 10.1039/d5sc03155a.
2
Supramolecular Materials and Strategies for Bioorthogonal Chemical Transformations.用于生物正交化学转化的超分子材料与策略
Chem Rev. 2025 Aug 13;125(15):7223-7274. doi: 10.1021/acs.chemrev.5c00047. Epub 2025 Aug 1.
3
Cis-Chelating Diphosphanes for Intracavity Nickel(II)-Catalyzed Ethylene Oligomerization.
用于腔内镍(II)催化乙烯齐聚反应的顺式螯合二膦烷
Chemistry. 2025 Jun 17;31(34):e202501188. doi: 10.1002/chem.202501188. Epub 2025 May 24.
4
Nanoconfinement Effects in Electrocatalysis and Photocatalysis.电催化和光催化中的纳米限域效应
Small. 2025 Apr;21(13):e2411184. doi: 10.1002/smll.202411184. Epub 2025 Feb 24.
5
Computational Study of Alkyne-Acid Cycloisomerization in Gold-Functionalized Resorcinarene Cavitand.金功能化间苯二酚杯芳烃穴状化合物中炔酸环异构化的计算研究
Chemistry. 2025 Apr 4;31(20):e202404480. doi: 10.1002/chem.202404480. Epub 2025 Mar 10.
6
Exploring New Bioorthogonal Catalysts: Scaffold Diversity in Catalysis for Chemical Biology.探索新型生物正交催化剂:化学生物学催化中的支架多样性
Adv Sci (Weinh). 2025 Mar;12(9):e2404431. doi: 10.1002/advs.202404431. Epub 2025 Feb 7.
7
London dispersion driven compaction of coordination cages in the gas-phase - a combined ion mobility and theoretical study.气相中伦敦色散驱动的配位笼压实——离子迁移率与理论相结合的研究
Chem Sci. 2024 Oct 14;15(46):19264-72. doi: 10.1039/d4sc04786a.
8
Harnessing a Pd Water-Soluble Molecular Capsule as a Size-Selective Catalyst for Targeted Oxidation of Alkyl Aromatics.利用钯水溶性分子胶囊作为尺寸选择性催化剂用于烷基芳烃的靶向氧化。
JACS Au. 2024 Aug 15;4(8):3238-3247. doi: 10.1021/jacsau.4c00539. eCollection 2024 Aug 26.
9
Bioinspired Binding and Conversion of Linear Monoterpenes by Polyaromatic Coordination Capsules.多芳族配位胶囊对线性单萜的生物启发式结合与转化
ACS Org Inorg Au. 2024 May 16;4(4):410-417. doi: 10.1021/acsorginorgau.4c00013. eCollection 2024 Aug 7.
10
Self-assembled molecular hybrids comprising lacunary polyoxometalates and multidentate imidazole ligands.由缺位多金属氧酸盐和多齿咪唑配体组成的自组装分子杂化物。
Chem Sci. 2024 May 16;15(24):9281-9286. doi: 10.1039/d4sc02384f. eCollection 2024 Jun 19.