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Synthesis of novel N-heterocyclic carbene-palladium complexes and their catalytic activity

机译:新型N-杂环卡宾 - 钯配合物的合成及其催化活性

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摘要

Chapter 1: Gives the reader a background on carbenes paying particular attention to N-heterocyclic carbenes (NHCs). The chapter describes NHC’s electronic and structural properties and their behaviour as ligands. The recent usage of NHC-palladium complexes as catalysts for cross-coupling reactions is explored.udChapter 2: Provides a background on NHC-palladium complexes bearing N-donors as throwaway ligands, highlighting the importance of throw-away ligands on catalytic activity. The chapter describes the preparation of a number of novel NHC-palladium complexes bearing throw-away ligands and the activity of (IPr*)PdCl2(TEA) in Buchwald-Hartwig aminations is explored.udChapter 3: Provides a background on the Mizoroki Heck reaction, focusing on the importance of charged intermediates in the process. Then reviews the current development of anionic NHC-palladium complexes in the literature. An account of the discovery and preparation of novel [(NHC)PdCl3[TBA] complexes and the catalytic activity of [(SIPr)PdCl3[TBA] in Mizoroki-Heck coupling reactions is given. A plausible Amotore-Jutand type mechanism is proposed which is supported by DFT calculations provided by research collaborators.udChapter 4: Provides a background on C-H activation reactions catalysed by palladium compounds with particular focus on acetoxylation reactions. The chapter describes the synthesis of [(NHC)PdCl2X][Y] complexes including the development of [(IMes)PdCl2OAc][TBA] and its performance in acetoxylation reactions. A proposed mechanism for the reaction of [(IMes)PdCl2OAc][TBA] is discussed, using experimental observations.
机译:第1章:为读者提供有关卡宾的背景知识,尤其要注意N-杂环卡宾(NHC)。本章介绍了NHC的电子和结构特性及其作为配体的行为。 ud第2章:提供了带有N-供体作为一次性配体的NHC-钯配合物的背景,强调了一次性配体对催化活性的重要性。本章介绍了许多带有可抛弃配体的新型NHC-钯配合物的制备,并探讨了Buchwald-Hartwig胺化中(IPr *)PdCl2(TEA)的活性。 ud第3章:为Mizoroki Heck提供背景反应,着重于过程中带电中间体的重要性。然后在文献中回顾了阴离子NHC-钯配合物的最新发展。给出了新型[(NHC)PdCl3 [TBA]配合物的发现和制备以及[(SIPr)PdCl3 [TBA]在Mazoroki-Heck偶联反应中的催化活性)。提出了一种可行的Amotore-Jutand型机理,该机理得到了研究合作者提供的DFT计算的支持。第四章:提供了钯化合物催化的C-H活化反应的背景,特别侧重于乙酰氧基化反应。本章介绍了[(NHC)PdCl2X] [Y]配合物的合成,包括[(IMes)PdCl2OAc] [TBA]的开发及其在乙酰氧基化反应中的性能。利用实验观察结果,讨论了[(IMes)PdCl2OAc] [TBA]反应的拟议机理。

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    Guest Daniel P;

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  • 年度 2017
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