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[((η5-trimethyl(2,3,4,5-tetramethyl-2,4-cyclopentadienyl)silane(-H))Y(μ-H)2)4(tetrahydrofuran)2] | 666748-01-2

中文名称
——
中文别名
——
英文名称
[((η5-trimethyl(2,3,4,5-tetramethyl-2,4-cyclopentadienyl)silane(-H))Y(μ-H)2)4(tetrahydrofuran)2]
英文别名
[((η(5)-C5Me4SiMe3)Y)4(μ-H)4(μ3-H)4(THF)2]
[((η5-trimethyl(2,3,4,5-tetramethyl-2,4-cyclopentadienyl)silane(-H))Y(μ-H)2)4(tetrahydrofuran)2]化学式
CAS
666748-01-2
化学式
C56H108O2Si4Y4
mdl
——
分子量
1281.44
InChiKey
HOGLNEGQLIJZKY-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为反应物:
    参考文献:
    名称:
    阳离子稀土多氢化物配合物:1,3-环己二烯的顺式1,4-选择性聚合的合成,结构和催化活性。
    摘要:
    DOI:
    10.1002/anie.200603450
  • 作为产物:
    描述:
    四氢呋喃[(η5-trimethyl(2,3,4,5-tetramethyl-2,4-cyclopentadienyl)silane(-H))Y(N,N,2-trimethylaniline(-H))2]氢气四氢呋喃 为溶剂, 以22%的产率得到[((η5-trimethyl(2,3,4,5-tetramethyl-2,4-cyclopentadienyl)silane(-H))Y(μ-H)2)4(tetrahydrofuran)2]
    参考文献:
    名称:
    Tetra-, Penta-, and Hexanuclear Yttrium Hydride Clusters from Half-Sandwich Bis(aminobenzyl) Complexes Containing Various Cyclopentadienyl Ligands
    摘要:
    The novel series of half-sandwich tetrahydrofuran (THF)-free yttrium bis(arninobenzyl) complexes [(C(5)Me(4)R)-Y(CH(2)C(6)H(4)NMe(2-o))(2)] (R = SiMe(3) (1a), Me (1b), Et (1c), H (1d)) was prepared by treatment of [Y(CH(2)C(6)H(4)NMe(2-o))(3)] with C(5)Me(4)RH, and their reactions with H(2) and with PhSiH(3) in aromatic solvents or in THF were examined. The reaction of la with H(2) in benzene gave the pentanudear yttrium decahydride complex [{Cp'Y(mu-H)(2)}(5)] (Cp' = eta(5)-C(5)Me(4)SiMe(3)) (3), which could not be obtained by the reaction of the corresponding THF-coordinated dialkyl complex [Cp'Y(CH(2)SiMe(3))(2)(THF)] with H(2). The reaction of 1b with H(2) in toluene gave the partially hydrogenated tetranudear mixed aminobenzyl/hydride complex [(Cp*Y)(2)(CH(2)C(6)H(4)NMe(2-o))(mu-H)(3)](2) (4; Cp* = eta(5)-C(5)Me(5)), and no further hydrogenation reaction occurred, whereas the corresponding reaction of 1b with H(2) in THF gave the pentanuclear yttrium polyhydride complex [{Cp*Y(mu-H)(2)}(5) (THF)(2)] (5). Hydrogenolysis of the sterically less demanding C(5)Me(4)H-ligated complex 1d with H(2) in THF gave the tetranuclear octahydride complex [{Cp(H)Y(mu-H)(2)}(4)(THF)(4)] (6; Cp(H) = eta(5)-C(5)Me(4)H), which has one coordinating THF ligand on each metal atom. The hexanuclear yttrium dodecahydride complex {[Cp*Y(mu-H)(2)](6)} (7) was obtained by treatment of 1b with PhSiH(3) in benzene. The structures of 1a,b,d, 3, 4, {{(C(5)Me(4)Et)Y(mu-H)(2)}(5)(THF)(2)] (5'), 6, and 7 were determined by X-ray single-crystal diffraction studies.
    DOI:
    10.1021/om1012055
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文献信息

  • Synthesis and Characterization of a Tetranuclear Hydride Cluster of Yttrium [{(η<sup>5</sup>‐C<sub>5</sub>Me<sub>4</sub>SiMe<sub>3</sub>)Y}<sub>4</sub>(μ‐H)<sub>4</sub>(μ<sub>3</sub>‐H)<sub>4</sub>(THF)<sub>2</sub>]
    作者:Kai C. Hultzsch、Peter Voth、Thomas P. Spaniol、Jun Okuda
    DOI:10.1002/zaac.200300063
    日期:2003.7
    Abstract

    Hydrogenolysis of the dialkyl complexes [Y(η5‐C5Me4SiMe2R)(CH2SiMe3)2(THF)] (1a, R = Me; 1b, R = Ph) results in the formation of the tetranuclear dihydrido complexes [(η5‐C5Me4SiMe2R)Y}4(μ‐H)43‐H)4(THF)2] (2a, R = Me; 2b, R = Ph), characterized by NMR spectroscopy. 2a was studied by single crystal X‐ray diffraction. In the solid state, an unsymmetrical tetrahedral configuration of four [Y(η5‐C5Me4SiMe3)] units is observed, two of which contain each one molecule of THF. Each yttrium atom is bonded to two μ2‐ as well as three μ3‐bridging hydrido ligands.

    摘要氢解二烷基络合物 [Y(η5-C5Me4SiMe2R)(CH2SiMe3)2(THF)](1a,R = Me;1b,R = Ph),从而形成四核二氢配合物[(η5-C5Me4SiMe2R)Y}4(μ-H)4(μ3-H)4(THF)2](2a,R = Me;2b,R = Ph),并通过核磁共振光谱进行表征。对 2a 进行了单晶 X 射线衍射研究。在固态下,观察到由四个[Y(η5-C5Me4SiMe3)]单元组成的非对称四面体构型,其中两个单元各含有一分子 THF。每个原子都与两个 μ2- 和三个 μ3 桥接的氢化物配位体结合。
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