Institut für Anorganische Chemie, Universität Regensburg, 93040 Regensburg (Germany) http://www.uni-regensburg.de/chemie-pharmazie/anorganische-chemie-scheer/
Angew Chem Int Ed Engl. 2015 Mar 27;54(14):4392-6. doi: 10.1002/anie.201411451. Epub 2015 Feb 10.
By the reaction of [NacnacCuCH3CN] with white phosphorus (P4) and yellow arsenic (As4), the stabilization and enclosure of the intact E4 tetrahedra are realized and the disubstituted complexes [(NacnacCu)2(μ,η(2:2)-E4)] (1 a: E=P, 1 b: E=As) are formed. The mono-substituted complex [NacnacCu(η(2)-P4)] (2), was detected by the exchange reaction of 1 a with P4 and was only isolated using low-temperature work-up. All products were comprehensively spectroscopically and crystallographically characterized. The bonding situation in the products as intact E4 units (E=P, As) was confirmed by theory and was experimentally proven by the pyridine promoted release of the bridging E4 tetrahedra in 1.
通过[NacnacCuCH3CN]与白磷(P4)和黄砷(As4)的反应,实现了完整 E4 四面体的稳定和封闭,并形成了双取代配合物[(NacnacCu)2(μ,η(2:2)-E4)](1a:E=P,1b:E=As)。通过 1a 与 P4 的交换反应检测到单取代配合物[NacnacCu(η(2)-P4)](2),但仅通过低温处理分离得到。所有产物均进行了全面的光谱和晶体学表征。产物中完整 E4 单元(E=P,As)的键合情况通过理论得到确认,并通过吡啶促进 1 中桥接 E4 四面体的释放得到实验验证。