Institut für Anorganische und Analytische Chemie and NRW Graduate School of Chemistry, Westfälische Wilhelms-Universität Münster, Corrensstrasse 30, 48149, Münster, Germany.
Institute of Advanced Materials (INAM), Universitat Jaume I, Avenida Vicente Sos Baynat, 12071, Castellon, Spain.
Angew Chem Int Ed Engl. 2017 Jun 19;56(26):7393-7397. doi: 10.1002/anie.201702637. Epub 2017 May 23.
Highly selective, narcissistic self-sorting has been observed in the one-pot synthesis of three organometallic molecular cylinders of type M {L-(NHC) } (M=Ag , Au ; L=1,3,5-benzene, triphenylamine, or 1,3,5-triphenylbenzene) from L-(NHC) and silver(I) or gold(I) ions. The molecular cylinders contain only one type of tris-NHC ligand with no crossover products detectable. Transmetalation of the tris-NHC ligands from Ag to Au in a one-pot reaction with retention of the supramolecular structures is also demonstrated. High-fidelity self-sorting was also observed in the one-pot reaction of benzene-bridged tris-NHC and tetrakis-NHC ligands with Ag O. This study for the first time extends narcissistic self-sorting in metal-ligand interactions from Werner-type complexes to organometallic derivatives.
在一锅法合成三种有机金属分子柱M{ L-(NHC)} (M=Ag,Au;L=1,3,5-苯、三苯胺或 1,3,5-三苯基苯)的过程中,观察到了高度选择性的、自恋型的自分类现象,其中 L-(NHC)和银(I)或金(I)离子反应。这些分子柱只含有一种类型的三-NHC 配体,没有可检测到的交叉产物。还证明了在一锅反应中,通过从 Ag 到 Au 的转金属反应,同时保留超分子结构,可以实现三-NHC 配体的转金属反应。在苯桥接三-NHC 和四-NHC 配体与 Ag O 的一锅反应中,也观察到了高保真的自分类。这项研究首次将金属-配体相互作用中的自恋型自分类从 Werner 型配合物扩展到有机金属衍生物。