Qi Ruipeng, Liu Bao, Xu Xiaoping, Yang Zijian, Yao Yingming, Zhang Yong, Shen Qi
Department of Chemistry and Chemical Engineering, Dushu Lake Campus, Suzhou University, Suzhou, 215123, PR China.
Dalton Trans. 2008 Oct 7(37):5016-24. doi: 10.1039/b804914a. Epub 2008 Jul 23.
The synthesis, characterization and reactivity of heteroleptic rare earth metal complexes supported by the carbon-bridged bis(phenolate) ligand 2,2'-methylene-bis(6-tert-butyl-4-methyl-phenoxo) (MBMP2-) are described. Reaction of (C5H5)3Ln(THF) with MBMPH2 in a 1:1.5 molar ratio in THF at 50 degrees C produced the heteroleptic rare earth metal bis(phenolate) complexes (C5H5)Ln(MBMP)(THF)n (Ln=La, n=3 (); Ln=Yb (), Y (), n=2) in nearly quantitative yields. The residual C5H5- groups in complexes to can be substituted by the bridged bis(phenolate) ligands at elevated temperature to give the neutral rare earth metal bis(phenolate) complexes, and the ionic radii have a profound effect on the structures of the final products. Complex reacted with MBMPH2 in a 1:0.5 molar ratio in toluene at 80 degrees C to produce a dinuclear complex (MBMP)La(THF)(micro-MBMP)2La(THF)2 () in good isolated yield; whereas complexes and reacted with MBMPH2 under the same conditions to give (MBMP)Ln(MBMPH)(THF)2 (Ln=Yb (), Y ()) as the final products, in which one hydroxyl group of the phenol is coordinated to the rare earth metal in a neutral fashion. The reactivity of complexes and with some metal alkyls was explored. Reaction of complex with 1 equiv. of AlEt3 in toluene at room temperature afforded unexpected ligand redistributed products, and a discrete ion pair ytterbium complex [(MBMP)Yb(THF)2(DME)][(MBMP)2Yb(THF)2] () was isolated in moderate yield. Furthermore, reaction of complex with 1 equiv. of ZnEt2 in toluene gave a ligand redistributed complex [(micro-MBMP)Zn(THF)]2 () in reasonable isolated yield. Similar reaction of complex with ZnEt2 also afforded complex ; whereas the reaction of complex with 1 equiv. of n-BuLi in THF afforded the heterodimetallic complex [(THF)Yb(MBMP)2Li(THF)2] (). All of these complexes were well characterized by elemental analyses, IR spectra, and single-crystal structure determination, in the cases of complexes , and -.
描述了由碳桥联双(酚盐)配体2,2'-亚甲基双(6-叔丁基-4-甲基苯氧基)(MBMP2-)支撑的杂配稀土金属配合物的合成、表征及反应活性。在50℃下,(C5H5)3Ln(THF)与MBMPH2以1:1.5的摩尔比在THF中反应,几乎定量地生成了杂配稀土金属双(酚盐)配合物(C5H5)Ln(MBMP)(THF)n(Ln = La,n = 3();Ln = Yb(),Y(),n = 2)。配合物中的残余C5H5-基团在高温下可被桥联双(酚盐)配体取代,生成中性稀土金属双(酚盐)配合物,且离子半径对最终产物的结构有深远影响。配合物在80℃下与甲苯中的MBMPH2以1:0.5的摩尔比反应,以良好的分离产率生成双核配合物(MBMP)La(THF)(μ-MBMP)2La(THF)2();而配合物和在相同条件下与MBMPH2反应,得到(MBMP)Ln(MBMPH)(THF)2(Ln = Yb(),Y())作为最终产物,其中酚的一个羟基以中性方式与稀土金属配位。研究了配合物和与一些金属烷基化合物的反应活性。配合物与1当量的AlEt3在室温下于甲苯中反应,得到意想不到的配体重新分布产物,并以中等产率分离得到离散离子对镱配合物[(MBMP)Yb(THF)2(DME)][(MBMP)2Yb(THF)2]()。此外,配合物与1当量的ZnEt2在甲苯中反应,以合理的分离产率得到配体重新分布的配合物[(μ-MBMP)Zn(THF)]2()。配合物与ZnEt2的类似反应也得到配合物;而配合物与1当量的n-BuLi在THF中反应得到异双核配合物[(THF)Yb(MBMP)2Li(THF)2]()。所有这些配合物均通过元素分析、红外光谱和单晶结构测定进行了充分表征,对于配合物、和-的情况也是如此。