Wolf Julian, Huber Florian, Erochok Nikita, Heinen Flemming, Guérin Vincent, Legault Claude Y, Kirsch Stefan F, Huber Stefan M
Fakultät für Chemie und Biochemie, Ruhr-Universität Bochum, Universitätsstraße 150, 44801, Bochum, Germany.
Organic Chemistry, Bergische Universität Wuppertal, Gaussstrasse 20, 42119, Wuppertal, Germany.
Angew Chem Int Ed Engl. 2020 Sep 14;59(38):16496-16500. doi: 10.1002/anie.202005214. Epub 2020 Jul 10.
In recent years, the non-covalent interaction of halogen bonding (XB) has found increasing application in organocatalysis. However, reports of the activation of metal-ligand bonds by XB have so far been limited to a few reactions with elemental iodine or bromine. Herein, we present the activation of metal-halogen bonds by two classes of inert halogen bond donors and the use of the resulting activated complexes in homogenous gold catalysis. The only recently explored class of iodolium derivatives were shown to be effective activators in two test reactions and their activity could be modulated by blocking of the Lewis acidic sites. Bis(benzimidazolium)-based halogen bonding activators provided even more rapid conversion, while the non-iodinated reference compound showed little activity. The role of halogen bonding in the activation of metal-halogen bonds was further investigated by NMR experiments and DFT calculations, which support the mode of activation occurring via halogen bonding.
近年来,卤键(XB)的非共价相互作用在有机催化中的应用越来越广泛。然而,迄今为止,关于卤键对金属-配体键的活化作用的报道仅限于少数与单质碘或溴的反应。在此,我们展示了两类惰性卤键供体对金属-卤键的活化作用,以及由此产生的活化配合物在均相金催化中的应用。最近才被研究的碘鎓衍生物在两个测试反应中被证明是有效的活化剂,并且它们的活性可以通过封锁路易斯酸性位点来调节。基于双(苯并咪唑鎓)的卤键活化剂能实现更快的转化,而未碘化的参考化合物几乎没有活性。通过核磁共振实验和密度泛函理论计算进一步研究了卤键在金属-卤键活化中的作用,这些研究支持了通过卤键发生的活化模式。