An Unusual Organoyttrium Alkyl Complex Containing a [C5HMe3(eta(3)-CH2)-C5H4N-kappa](-) Ligand and an Elusive Cyclopentadienide-Based Scandium Tuck-Over Zwitterion Obtained by C-H Bond Activation
文献类型：期刊论文
| 作者 | Jian, Zhongbao1,2; Cui, Dongmei1 |
| 刊名 | CHEMISTRY-A EUROPEAN JOURNAL
 |
| 出版日期 | 2011-12-01 |
| 卷号 | 17期号:51页码:14578-14585 |
| 关键词 | C-h Activation Coordination Modes Cyclopentadienyl Ligands Rare Earths Zwitterions |
| ISSN号 | 0947-6539 |
| DOI | 10.1002/chem.201102378 |
| 英文摘要 | The acid-base reaction between Y(CH2SiMe3)(3)(thf)(2) and the pyridyl-functionalized cyclopentadienyl (Cp) ligand C5Me4H-C5H4N (1 equiv) at 0 degrees C afforded a mixture of two products: (eta(5):kappa-C5Me4-C5H4N)Y-(CH2SiMe3) (2)(thf) (1a) and (eta(5):kappa-C5Me4-C5H4N)(2)Y-CH2SiMe3 (1b), in a 5: 2 ratio. Addition of the same ligand (2 equiv) to Y(CH2SiMe3)(3)(thf)(2), however, generated 1b together with the novel complex 1c, the first well defined yttrium mono(alkyl) complex (eta(5):kappa-C5Me4-C5H4N)[C5HMe3(eta(3)-CH2)-C5H4N-kappa] Y(CH2SiMe3) containing a rare k/eta(3)-allylic coordination mode in which the C-H bond activation occurs unexpectedly with the allylic methyl group rather than conventionally on Cp ring. If the central metal was changed to lutetium, the equimolar reaction between Lu(CH2SiMe3)(3)(thf)(2) and C5Me4H-C5H4N exclusively afforded the bis(alkyl) product (eta(5):kappa C5Me4-C5H4N)Lu(CH2SiMe3)(2) (thf) (2a). Similarly, the reaction between the ligand (2 equiv) and Lu(CH2SiMe3)(3)(thf)(2) gave the mono(alkyl) complex (eta(5):kappa-C5Me4-C5H4N)(2)LuCH2SiMe3 (2b), in which no ligand redistribution was observed. Strikingly, treatment of Sc(CH2SiMe3)(3)-(thf) 2 with C5Me4H-C5H4N in either 1:1 or 1:2 ratio at 0 degrees C generated the first cyclopentadienide-based scandium zwitterionic "tuck-over" complex 3, (eta(5):kappa-C5Me4H-C5H4N)Sc(thf)[eta-eta(5):eta(1):kappa-C5Me3(CH2)-C5H4N] Sc(CH2SiMe3)(3). In the zwitterion, the dianionic ligand [C5Me3(CH2)-C5H4N](2-) binds both to Scl(3+) and to Sc2(3+), in eta(5) and eta(1)/k modes. In addition, the reaction chemistry, the molecular structures, and the mechanism are also discussed in detail. |
| 语种 | 英语 |
| WOS记录号 | WOS:000298542300029 |
| 出版者 | WILEY-V C H VERLAG GMBH |
| 源URL | [http://ir.iccas.ac.cn/handle/121111/73817]  |
| 专题 | 中国科学院化学研究所 |
| 通讯作者 | Cui, Dongmei |
| 作者单位 | 1.Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China 2.Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China |
| 推荐引用方式 GB/T 7714 | Jian, Zhongbao,Cui, Dongmei. An Unusual Organoyttrium Alkyl Complex Containing a [C5HMe3(eta(3)-CH2)-C5H4N-kappa](-) Ligand and an Elusive Cyclopentadienide-Based Scandium Tuck-Over Zwitterion Obtained by C-H Bond Activation[J]. CHEMISTRY-A EUROPEAN JOURNAL,2011,17(51):14578-14585. |
| APA | Jian, Zhongbao,&Cui, Dongmei.(2011).An Unusual Organoyttrium Alkyl Complex Containing a [C5HMe3(eta(3)-CH2)-C5H4N-kappa](-) Ligand and an Elusive Cyclopentadienide-Based Scandium Tuck-Over Zwitterion Obtained by C-H Bond Activation.CHEMISTRY-A EUROPEAN JOURNAL,17(51),14578-14585. |
| MLA | Jian, Zhongbao,et al."An Unusual Organoyttrium Alkyl Complex Containing a [C5HMe3(eta(3)-CH2)-C5H4N-kappa](-) Ligand and an Elusive Cyclopentadienide-Based Scandium Tuck-Over Zwitterion Obtained by C-H Bond Activation".CHEMISTRY-A EUROPEAN JOURNAL 17.51(2011):14578-14585. |
入库方式： OAI收割
来源：化学研究所
浏览0
下载0
收藏0
其他版本
除非特别说明，本系统中所有内容都受版权保护，并保留所有权利。