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