Zhang Kehua, Zhang Wu, Wang Shaowu, Sheng Enhong, Yang Gaosheng, Xie Meihua, Zhou Shuangliu, Feng Yan, Mao Lili, Huang Zixiang
Institute of Organic Chemistry, School of Chemistry and Materials Science, Anhui Normal University, Wuhu, Anhui 241000, China.
Dalton Trans. 2004 Apr 7(7):1029-37. doi: 10.1039/b314115b. Epub 2004 Feb 26.
The interaction of methoxyethyl functionalized indene compounds (C(9)H(6)-1-R-3-CH(2)CH(2)OMe, R =t-BuNHSiMe(2)(1), Me(3)Si (2), H (3)) with (Me(3)Si)(2)NLn(mu-Cl)Li(THF)(3)(Ln=Yb (4), Eu (5)) produced a series of new ytterbium(II) and europium(II) complexes via tandem silylamine elimination/homolysis of the Ln-N (Ln=Yb, Eu) bond. Treatment of the lanthanide(III) amides (Me(3)Si)(2)NLn(mu-Cl)Li(THF)(3)(Ln=Yb (4), Eu (5) with 2 equiv. of, 1,2 and 3, respectively, produced, after workup, the ytterbium(II) complexes eta5:eta1-Me(2)Si(MeOCH(2)CH(2)C(9)H(5))(NHBu-t)Yb(II) (6), (eta5:eta1-MeOCH(2)CH(2)C(9)H(5)SiMe(3))(2)Yb(II) (7), (eta5:eta1-MeOCH(2)CH(2)C(9)H(6))(2)Yb(II)(8) and the corresponding europium(II) complexes eta5:eta1-Me(2)Si(MeOCH(2)CH(2)C(9)H(5))(NHBu-t)Eu(II)(9), (eta5:eta1-MeOCH(2)CH(2)C(9)H(5)SiMe(3))(2)Eu(II)(10) and (eta5:eta1-MeOCH(2)CH(2)C(9)H(6))(2)Eu(II)(11) in moderate to good yield. In contrast, interaction of the corresponding indene compounds 1, 2 or 3 with the lanthanide amides (Me(3)Si)(2)NLn (Ln = Yb, Eu) was not observed, while addition of 0.5 equiv. of anhydrous LiCl to the corresponding reaction mixture produced, after workup, the corresponding ytterbium(II) or europium(II) complexes. All the new compounds were fully characterized by spectroscopic and elemental analyses. The structures of complexes, and were determined by single-crystal X-ray analyses. The catalytic activity of all the ytterbium(II) and europium(II) complexes on MMA polymerization was examined. It was found that all the ytterbium(II) and europium(II) complexes can function as single-component MMA polymerization catalysts. The temperature, solvent and ligand effects on the catalytic activity were studied.
甲氧基乙基官能化茚化合物(C(9)H(6)-1-R-3-CH(2)CH(2)OMe,R =叔丁基NHSiMe(2)(1)、Me(3)Si (2)、H (3))与(Me(3)Si)(2)NLn(μ-Cl)Li(THF)(3)(Ln = Yb (4)、Eu (5))相互作用,通过串联硅胺消除/Ln-N(Ln = Yb、Eu)键的均裂反应生成了一系列新的镱(II)和铕(II)配合物。分别用2当量的1、2和3处理镧系(III)酰胺(Me(3)Si)(2)NLn(μ-Cl)Li(THF)(3)(Ln = Yb (4)、Eu (5)),经后处理得到了产率适中至良好的镱(II)配合物η5:η1-Me(2)Si(MeOCH(2)CH(2)C(9)H(5))(NHBu-t)Yb(II) (6)、(η5:η1-MeOCH(2)CH(2)C(9)H(5)SiMe(3))(2)Yb(II) (7)、(η5:η1-MeOCH(2)CH(2)C(9)H(6))(2)Yb(II)(8)以及相应的铕(II)配合物η5:η1-Me(2)Si(MeOCH(2)CH(2)C(9)H(5))(NHBu-t)Eu(II)(9)、(η5:η1-MeOCH(2)CH(2)C(9)H(5)SiMe(3))(2)Eu(II)(10)和(η5:η1-MeOCH(2)CH(2)C(9)H(6))(2)Eu(II)(11)。相比之下,未观察到相应的茚化合物1、2或3与镧系酰胺(Me(3)Si)(2)NLn(Ln = Yb、Eu)的相互作用,而向相应反应混合物中加入0.5当量的无水LiCl,经后处理得到了相应的镱(II)或铕(II)配合物。所有新化合物均通过光谱和元素分析进行了全面表征。配合物6、7、8、9、10和11的结构通过单晶X射线分析确定。考察了所有镱(II)和铕(II)配合物对甲基丙烯酸甲酯(MMA)聚合的催化活性。发现所有镱(II)和铕(II)配合物均可作为单组分MMA聚合催化剂。研究了温度、溶剂和配体对催化活性的影响。