• 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

Highly Active Ruthenium Catalysts for Olefin Metathesis: The Synergy of N-Heterocyclic Carbenes and Coordinatively Labile Ligands.

作者信息

Weskamp T, Kohl FJ, Hieringer W, Gleich D, Herrmann WA

机构信息

Anorganisch-chemisches Institut der Technischen Universität München, Lichtenbergstrasse 4, D-85747 Garching (Germany).

出版信息

Angew Chem Int Ed Engl. 1999 Aug;38(16):2416-2419. doi: 10.1002/(sici)1521-3773(19990816)38:16<2416::aid-anie2416>3.0.co;2-#.

DOI:10.1002/(sici)1521-3773(19990816)38:16<2416::aid-anie2416>3.0.co;2-#
PMID:10458807
Abstract

Two N-heterocyclic carbene ligands at once may be one too many, at least if you intend to have highly active ruthenium catalysts for olefin metathesis. Density functional calculations recommend the replacement of the second carbene ligand in the successful ROMP catalysts 1 by coordinatively more labile ligands as in 2 or 3. In both cases, the catalytic activity is greatly improved.

摘要

相似文献

1
Highly Active Ruthenium Catalysts for Olefin Metathesis: The Synergy of N-Heterocyclic Carbenes and Coordinatively Labile Ligands.
Angew Chem Int Ed Engl. 1999 Aug;38(16):2416-2419. doi: 10.1002/(sici)1521-3773(19990816)38:16<2416::aid-anie2416>3.0.co;2-#.
2
Ruthenium Olefin Metathesis Catalysts Bearing a Macrocyclic N-Heterocyclic Carbene Ligand: Improved Stability and Activity.钌烯烃复分解催化剂,带有大环 N-杂环卡宾配体:稳定性和活性提高。
Angew Chem Int Ed Engl. 2022 Jun 13;61(24):e202201472. doi: 10.1002/anie.202201472. Epub 2022 Apr 13.
3
Ruthenium Olefin Metathesis Catalysts Featuring N-Heterocyclic Carbene Ligands Tagged with Isonicotinic and 4-(Dimethylamino)benzoic Acid Rests: Evaluation of a Modular Synthetic Strategy.钌烯烃复分解催化剂,其特征为带有异烟酸和 4-(二甲氨基)苯甲酸残基的 N-杂环卡宾配体:模块化合成策略的评估。
Molecules. 2021 Aug 28;26(17):5220. doi: 10.3390/molecules26175220.
4
Ruthenium Complexes Bearing Thiophene-Based Unsymmetrical N-Heterocyclic Carbene Ligands as Selective Catalysts for Olefin Metathesis in Toluene and Environmentally Friendly 2-Methyltetrahydrofuran.钌配合物负载噻吩基不对称 N-杂环卡宾配体作为在甲苯和环境友好的 2-甲基四氢呋喃中烯烃复分解反应的选择性催化剂。
Chemistry. 2018 Oct 12;24(57):15372-15379. doi: 10.1002/chem.201803460. Epub 2018 Sep 19.
5
Ruthenium Catalysts Supported by Amino-Substituted N-Heterocyclic Carbene Ligands for Olefin Metathesis of Challenging Substrates.由氨基取代的氮杂环卡宾配体支撑的钌催化剂用于具有挑战性底物的烯烃复分解反应
Chemistry. 2017 Feb 3;23(8):1950-1955. doi: 10.1002/chem.201604934. Epub 2017 Jan 18.
6
Ruthenium-based olefin metathesis catalysts coordinated with unsymmetrical N-heterocyclic carbene ligands: synthesis, structure, and catalytic activity.与不对称N-杂环卡宾配体配位的钌基烯烃复分解催化剂:合成、结构及催化活性
Chemistry. 2008;14(25):7545-56. doi: 10.1002/chem.200800470.
7
Synthesis of N-heterocyclic carbene ligands and derived ruthenium olefin metathesis catalysts.N-杂环卡宾配体的合成及衍生的钌烯烃复分解催化剂。
Nat Protoc. 2011 Jan;6(1):69-77. doi: 10.1038/nprot.2010.177. Epub 2010 Dec 16.
8
Ruthenium Complexes Featuring Unsymmetrical N-Heterocyclic Carbene Ligands-Useful Olefin Metathesis Catalysts for Special Tasks.钌配合物,具有不对称 N-杂环卡宾配体-用于特殊任务的有用的烯烃复分解催化剂。
Chem Rec. 2021 Dec;21(12):3648-3661. doi: 10.1002/tcr.202100126. Epub 2021 Jun 19.
9
Ruthenium-based olefin metathesis catalysts with monodentate unsymmetrical NHC ligands.具有单齿不对称NHC配体的钌基烯烃复分解催化剂。
Beilstein J Org Chem. 2018 Dec 28;14:3122-3149. doi: 10.3762/bjoc.14.292. eCollection 2018.
10
Ruthenium olefin metathesis catalysts featuring unsymmetrical N-heterocyclic carbenes.具有不对称 N-杂环卡宾的钌烯烃复分解催化剂。
Dalton Trans. 2016 Jan 14;45(2):561-71. doi: 10.1039/c5dt03758a.

引用本文的文献

1
Heterobimetallic Gold/Ruthenium Complexes Synthesized via Post-functionalization and Applied in Dual Photoredox Gold Catalysis.通过后功能化合成并应用于双光氧化还原金催化的异双金属金/钌配合物
Chemistry. 2022 Oct 12;28(57):e202201856. doi: 10.1002/chem.202201856. Epub 2022 Sep 1.
2
Synthesis of nano magnetic supported NHC-palladium and investigation of its applications as a catalyst in the Mizoroki-Heck cross-coupling reaction in HO.纳米磁性负载NHC-钯的合成及其在水相中作为催化剂用于 Mizoroki-Heck 交叉偶联反应的应用研究。
Heliyon. 2020 Sep 23;6(9):e04946. doi: 10.1016/j.heliyon.2020.e04946. eCollection 2020 Sep.
3
A Terminal Iron Nitrilimine Complex: Accessing the Terminal Nitride through Diazo N-N Bond Cleavage.
一种末端铁硝亚胺配合物:通过重氮 N-N 键裂解获得末端氮化物。
Angew Chem Int Ed Engl. 2019 Dec 16;58(51):18547-18551. doi: 10.1002/anie.201910428. Epub 2019 Oct 31.
4
Supported Catalysts Useful in Ring-Closing Metathesis, Cross Metathesis, and Ring-Opening Metathesis Polymerization.用于闭环复分解、交叉复分解和开环复分解聚合反应的负载型催化剂。
Polymers (Basel). 2016 Apr 12;8(4):140. doi: 10.3390/polym8040140.
5
Moving from Classical Ru-NHC to Neutral or Charged Rh-NHC Based Catalysts in Olefin Metathesis.烯烃复分解反应中从经典钌-N-杂环卡宾催化剂向中性或带电荷的铑-N-杂环卡宾催化剂的转变
Molecules. 2016 Jan 30;21(2):177. doi: 10.3390/molecules21020177.
6
Olefin metathesis in air.空气中的烯烃复分解反应。
Beilstein J Org Chem. 2015 Oct 30;11:2038-56. doi: 10.3762/bjoc.11.221. eCollection 2015.
7
A comprehensive study of olefin metathesis catalyzed by Ru-based catalysts.一项关于钌基催化剂催化烯烃复分解反应的综合研究。
Beilstein J Org Chem. 2015 Sep 29;11:1767-80. doi: 10.3762/bjoc.11.192. eCollection 2015.
8
Synthesis of the first radiolabeled 188Re N-heterocyclic carbene complex and initial studies on its potential use in radiopharmaceutical applications.首个放射性标记的188Re N-杂环卡宾配合物的合成及其在放射性药物应用中的潜在用途的初步研究。
J Labelled Comp Radiopharm. 2014 Jun 15;57(7):441-7. doi: 10.1002/jlcr.3203. Epub 2014 May 29.
9
Synthesis of the first poly(diaminosulfide)s and an investigation of their applications as drug delivery vehicles.首例聚二氨基硫化物的合成及其作为药物递送载体的应用研究。
Macromolecules. 2012 Jan 24;45(2):688-697. doi: 10.1021/ma2023167.
10
Grubbs and Hoveyda-Type Ruthenium Complexes Bearing a Cyclic Bent-Allene.带有环状弯曲丙二烯的格拉布斯和霍维达型钌配合物。
J Organomet Chem. 2011 Aug 15;696(17):2899-2903. doi: 10.1016/j.jorganchem.2011.03.010.