Liu Jingjing, Singh Kalyan, Dutta Sayan, Feng Zhongtao, Koley Debasis, Tan Gengwen, Wang Xinping
College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, China.
Department of Chemical Sciences, Indian Institute of Science Education and Research (IISER) Kolkata, Mohanpur 741246, India.
Dalton Trans. 2021 Apr 28;50(16):5552-5556. doi: 10.1039/d1dt00798j.
The reactions of dipotassium 3,4-dimethyl-2,5-bis(trimethylsilyl)-germole dianion K2[1] with YCl3 and CpYCl2 (Cp = cyclopentadienyl) in THF at room temperature afforded the dianion salt [(K-cryptand-222)2][1-YCl3] (K2[2]) and the dimeric complex [1-Y-Cp*]2 (3), respectively. While the polymeric complex {[(1)2-Y-K(toluene)]2}n (4) was obtained from the reaction of K2[1] and half molar equivalent of YCl3(THF)3.5 in toluene at 80 °C. The germole dianions in complexes 3 and 4 feature η5/η1 coordination interactions with the yttrium atoms. They represent the first examples of rare earth (RE) complexes containing RE-Ge bonds other than the RE-GeR3 structural type.
3,4 - 二甲基 - 2,5 - 双(三甲基硅基)锗茂二钾阴离子K₂[1]与YCl₃和CpYCl₂(Cp = 环戊二烯基)在室温下于四氢呋喃中反应,分别得到二阴离子盐[(K - 穴醚 - 222)₂][1 - YCl₃](K₂[2])和二聚配合物[1 - Y - Cp*]₂(3)。而聚合物配合物{[(1)₂ - Y - K(甲苯)]₂}ₙ(4)是由K₂[1]与半摩尔当量的YCl₃(THF)₃.₅在80℃的甲苯中反应得到的。配合物3和4中的锗茂二阴离子与钇原子具有η⁵/η¹配位相互作用。它们代表了除RE - GeR₃结构类型之外含RE - Ge键的稀土(RE)配合物的首个实例。