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烷氧基咪唑啉(NOHCs):基于氧化咪唑鎓核心的亲核卡宾。

-Alkoxyimidazolylidines (NOHCs): nucleophilic carbenes based on an oxidized imidazolium core.

机构信息

Institute of Organic Chemistry, Justus Liebig University, Heinrich-Buff-Ring 17,, 35392 Giessen, Germany.

Department of Organic Chemistry, National Technical University of Ukraine "Igor Sikorsky Kyiv Polytechnic Institute", Prosp. Peremohy 37, 03056 Kyiv, Ukraine.

出版信息

Chem Commun (Camb). 2022 Feb 1;58(10):1538-1541. doi: 10.1039/d1cc05696d.

Abstract

We report the first preparation of -alkoxyimidazolylidene (NOHC), a nucleophilic carbene based on an oxidized imidazolium core. The Arduengo-type analogous carbene center shows the most upfield C NMR shift compared to common NHCs. The obtained gold(I) complex of the carbene follows the C NMR upfield trend and shows the marked influence the alkoxy substituents. Similarly, the Se and N NMR shifts of a range of NOHC-selenium adducts show increased σ-donation and decreased π-back donation in the bonding with the nucleophile. This extension of the NHC family provides altered electronic properties for the use of such carbenes as ligands or catalysts.

摘要

我们首次制备了 -烷氧基咪唑基(NOHC),这是一种基于氧化咪唑鎓核心的亲核卡宾。与常见的 NHC 相比,Arduengo 型类似卡宾中心的 C NMR 位移出现在最场。所得卡宾的金(I)配合物遵循 C NMR 场位移趋势,并显示出烷氧基取代基的明显影响。同样,一系列 NOHC-硒加合物的 Se 和 N NMR 位移表明,在与亲核试剂键合时,σ-给电子能力增加,π-回供电子能力降低。这种 NHC 家族的扩展为将此类卡宾用作配体或催化剂提供了改变的电子性质。

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