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金属阳离子驱动的亚胺和腙配体的动态共价形成,表现出协同共催化和辅助胺效应。

Metal Cation-Driven Dynamic Covalent Formation of Imine and Hydrazone Ligands Displaying Synergistic Co-catalysis and Auxiliary Amine Effects.

作者信息

He Meixia, Lehn Jean-Marie

机构信息

Laboratoire de Chimie Supramoléculaire, Institut de Science et d'Ingénierie Supramoléculaires, Université de Strasbourg, 8 allée Gaspard Monge, 67000, Strasbourg, France.

出版信息

Chemistry. 2021 May 12;27(27):7516-7524. doi: 10.1002/chem.202100662. Epub 2021 Apr 28.

Abstract

Optimizing C=N bond formation and C/N component exchange has major significance in Dynamic Covalent Chemistry (DCC). Imine and hydrazone generation from their aldehyde, amine and hydrazine components showed large accelerations in presence of AgOTf or Zn(OTf) , up to 10 for the Zn(II)-(p-anisidine)imine complex. Zn(OTf) and auxiliary p-anisidine together accelerated 630 times the formation of the Zn(II)-hydrazone complex, revealing a strong synergistic effect, traced to very fast initial formation of the reactive Zn(II)-imine complex presenting a C=N bond metallo-activated towards reaction with the hydrazine component. Reactions involving more entities showed kinetically faster and thermodynamically simpler outputs due to dynamic competition within a mixture of higher complexity. Catalytic amounts of metal salts and auxiliary amine gave similar marked rate accelerations and turnover, indicating true catalysis. The synergistic effect achieved by combining metallo- and organo-catalysis points to a powerful co-catalysis strategy of bond-formation in DCC through interconnected chemical transformations.

摘要

在动态共价化学(DCC)中,优化C=N键的形成以及C/N组分交换具有重大意义。由醛、胺和肼组分生成亚胺和腙在AgOTf或Zn(OTf)存在下有显著加速,对于Zn(II)-(对甲氧基苯胺)亚胺配合物,加速倍数高达10倍。Zn(OTf)和辅助对甲氧基苯胺共同使Zn(II)-腙配合物的形成加速了630倍,揭示了一种强烈的协同效应,这归因于反应性Zn(II)-亚胺配合物的非常快速的初始形成,该配合物呈现出一个对与肼组分反应具有金属活化作用的C=N键。涉及更多实体的反应由于在更高复杂性混合物中的动态竞争而在动力学上更快且在热力学上更简单。催化量的金属盐和辅助胺产生了类似的显著速率加速和周转,表明是真正的催化作用。通过结合金属催化和有机催化实现的协同效应指向了一种通过相互关联的化学转化在DCC中进行键形成的强大共催化策略。

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