Institut für Anorganische Chemie, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074 Würzburg, Germany.
Inorg Chem. 2012 Feb 20;51(4):2679-88. doi: 10.1021/ic202638k. Epub 2012 Jan 26.
The microwave-assisted Pd-catalyzed Kumada-type cross-coupling reaction of iodinated carba-closo-dodecaborate anions requires smaller amounts of Grignard reagent and catalyst and results in higher yields in much shorter reaction times in comparison to a reaction with conventional heat transfer. 12-Ph(3)P-closo-1-CB(11)H(11) was identified as the side product of the cross-coupling reactions that use [PdCl(2)(PPh(3))(2)]. The inner salt, which is the first example for a {closo-1-CB(11)} cluster with a B-P bond, was selectively synthesized via a related microwave-assisted cross-coupling protocol and characterized by NMR spectroscopy, elemental analysis, and single-crystal X-ray diffraction. In addition, the crystal structures of the tetraethyl ammonium salts of 12-Ph-closo-1-CB(11)H(11), 12-(4-MeOC(6)H(4))-closo-1-CB(11)H(11), and 12-(H(2)C═(Me)CC≡C)-closo-1-CB(11)H(11) are described.
微波辅助钯催化的 Kumada 型交叉偶联反应需要较少的格氏试剂和催化剂,与传统传热反应相比,反应时间更短,产率更高。12-Ph(3)P-closo-1-CB(11)H(11)被确定为交叉偶联反应的副产物,该反应使用[PdCl(2)(PPh(3))(2)]。内盐是第一个具有 B-P 键的{closo-1-CB(11)}簇的例子,通过相关的微波辅助交叉偶联协议选择性合成,并通过 NMR 光谱、元素分析和单晶 X 射线衍射进行了表征。此外,还描述了[12-Ph-closo-1-CB(11)H(11)]-、[12-(4-MeOC(6)H(4))-closo-1-CB(11)H(11)]-和[12-(H(2)C═(Me)CC≡C)-closo-1-CB(11)H(11)]-的四乙铵盐的晶体结构。