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[Ru2(μ-(η(5)-C5H4)2SiMe2)(μ-CO)2(CO)2] | 178414-48-7

中文名称
——
中文别名
——
英文名称
[Ru2(μ-(η(5)-C5H4)2SiMe2)(μ-CO)2(CO)2]
英文别名
(Me2Si)[(η(5)-C5H4)Ru(CO)]2(μ-CO)2;((η5-C5H4)2SiMe2)Ru2(CO)4
[Ru2(μ-(η(5)-C5H4)2SiMe2)(μ-CO)2(CO)2]化学式
CAS
178414-48-7
化学式
C16H14O4Ru2Si
mdl
——
分子量
500.51
InChiKey
NLTFYKVRSWPIHK-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:
    描述:
    [Ru2(μ-(η(5)-C5H4)2SiMe2)(μ-CO)2(CO)2]二氯甲烷 为溶剂, 以77%的产率得到[Ru2(μ-(η(5)-C5H4)2SiMe2)(Br)2(CO)4]
    参考文献:
    名称:
    我2的Si(η 5 -C 5 H ^ 4)2 -Bridged双核钌化合物:[Ru中的X射线晶体结构2 {μ-(η 5 -C 5 H ^ 4)2森达2 }(CL)2(CO )4 ]和[茹2 {μ-(η 5 -C 5 H ^ 4)2森达2 }(μ-溴)(CO)4 ] [BF 4 ]
    摘要:
    双核四羰治疗复杂的[Ru 2 {μ-(η 5 -C 5 H ^ 4)2森达2 }(μ-CO)2(CO)2 ](1)与HBF 4在二氯甲烷中通向电加成一个质子的,得到桥接氢化物络合物的[Ru 2 {μ-(η 5 -C 5 H ^ 4)2森达2 }(μ-H)(CO)4 ] [BF 4 ](2)。配合物1也与Li反应[BHEt 3],得到桥接亚甲基复杂的[Ru 2 {μ-(η 5 -C 5 H ^ 4)2森达2 }(μ-CH 2)(μ-CO)(CO)2 ](3)。双核配合物的[Ru 2 {μ-(η 5 -C 5 H ^ 4)2森达2 }(X)2(CO)4 ](X =氯(4A),溴(图4b),和I(图4c))具有从配合物1与N的反应中以高收率合成-CH 2 Cl 2中的-氯代琥珀酰亚胺(X = Cl)和X 2(X = Br,I)。复杂的结构4A已经通过X射线晶体学显示围绕由桥接我连接各钌原子的三条腿的钢琴凳几何被确定2的Si(η
    DOI:
    10.1021/om980547a
  • 作为产物:
    描述:
    [Ru2(μ-(η(5)-C5H4)2SiMe2)(μ-H)(CO)4][BF4] 以 丙酮 为溶剂, 生成 [Ru2(μ-(η(5)-C5H4)2SiMe2)(μ-CO)2(CO)2]
    参考文献:
    名称:
    我2的Si(η 5 -C 5 H ^ 4)2 -Bridged双核钌化合物:[Ru中的X射线晶体结构2 {μ-(η 5 -C 5 H ^ 4)2森达2 }(CL)2(CO )4 ]和[茹2 {μ-(η 5 -C 5 H ^ 4)2森达2 }(μ-溴)(CO)4 ] [BF 4 ]
    摘要:
    双核四羰治疗复杂的[Ru 2 {μ-(η 5 -C 5 H ^ 4)2森达2 }(μ-CO)2(CO)2 ](1)与HBF 4在二氯甲烷中通向电加成一个质子的,得到桥接氢化物络合物的[Ru 2 {μ-(η 5 -C 5 H ^ 4)2森达2 }(μ-H)(CO)4 ] [BF 4 ](2)。配合物1也与Li反应[BHEt 3],得到桥接亚甲基复杂的[Ru 2 {μ-(η 5 -C 5 H ^ 4)2森达2 }(μ-CH 2)(μ-CO)(CO)2 ](3)。双核配合物的[Ru 2 {μ-(η 5 -C 5 H ^ 4)2森达2 }(X)2(CO)4 ](X =氯(4A),溴(图4b),和I(图4c))具有从配合物1与N的反应中以高收率合成-CH 2 Cl 2中的-氯代琥珀酰亚胺(X = Cl)和X 2(X = Br,I)。复杂的结构4A已经通过X射线晶体学显示围绕由桥接我连接各钌原子的三条腿的钢琴凳几何被确定2的Si(η
    DOI:
    10.1021/om980547a
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文献信息

  • Reactions of the Protonated Dinuclear Ruthenium Complex [{(<i>η</i><sup>5</sup>-C<sub>5</sub>H<sub>3</sub>)<sub>2</sub>(SiMe<sub>2</sub>)<sub>2</sub>}Ru<sub>2</sub>(CO)<sub>4</sub>(<i>μ</i>-H)]<sup>+</sup> with Nucleophiles
    作者:Maxim V. Ovchinnikov、Arkady M. Ellern、Ilia A. Guzei、Robert J. Angelici
    DOI:10.1021/ic010644n
    日期:2001.12.1
    [[(eta(5)-C(5)H(3))(2)(SiMe(2))(2)]Ru(2)(CO)(4)(mu-H)](+)BF(4)(-) (1H(+)BF(4)(-)), which features a protonated Ru-Ru bond, reacts with F(-) to give (eta(5)-C(5)H(5))(2)Ru(2)(CO)(4) (2), resulting from the cleavage of both SiMe(2) groups, with I(-) to give the Ru-Ru cleaved product [(eta(5)-C(5)H(3))(2)(SiMe(2))(2)]Ru(2)(CO)(4)(H)(I)(3), and with phosphines (PEt(3), PMe(2)Ph) to give [[(eta(5)-C(5)H(3)
    复合物[[(eta(5)-C(5)H(3))(2)(SiMe(2))(2)] Ru(2)(CO)(4)(mu-H)](+) BF(4)(-)(1H(+)BF(4)(-))具有质子化的Ru-Ru键,与F(-)反应生成(eta(5)-C(5)H( 5))(2)Ru(2)(CO)(4)(2),这是由于两个SiMe(2)基团均被I(-)裂解而得到的Ru-Ru裂解产物[(eta(5 )-C(5)H(3))(2)(SiMe(2))(2)] Ru(2)(CO)(4)(H)(I)(3)和膦类化合物(PEt( 3),PMe(2)Ph)给出[[(eta(5)-C(5)H(3))(2)(SiMe(2))(2)] Ru(2)(CO)(4 )(H)(PR(3))](+)(4a-b)。1H(+)BF(4)(-)与NaOMe在THF中反应生成[(eta(5)-C(5)H(4))(2)SiMe(2)] Ru(2)(CO)
  • Insertion of SnCl2 into the metal-metal bonds in bridged binuclear complexes (Me2E)[(η5-C5H4)M(CO)]2(μ-CO)2 (ESi, Ge; MFe, Ru. (The molecular structure of (Me2Ge)[(η5-C5H4)Fe(CO)2]2SnCl2
    作者:Yongqiang Zhang、Shansheng Xu、Gonglu Tian、Wei Zhang、Xiuzhong Zhou
    DOI:10.1016/s0022-328x(97)00312-4
    日期:1997.10
    The synthesis of bridged binuclear complexes (Me2E)[(eta(5)-C5H4)M(CO)](2)(mu-CO)(2) [E = Si, M = Ru (3); E = Ge, M = Fe (2), M = Ru (4)] is described. Insertion of SnCl2 into the metal-metal bonds in these complexes affords a type of hetero-nuclear cyclic metallic complexes (Me2E)[(eta(5)-C5H4)M(CO)(2)](2)SnCl2 [E = Si, M = Ru (7); E = Ge, M = Fe (6), M = Ru (8)]. Complex 6 reacts with Grignard reagents RMgX to yield alkyl (or aryl)-substituted analogues (Me2Ge)[(eta(5)-C5H4)Fe(CO)(2)](2)SnR2 [R = Me (9); R = Ph (10)]. AU of the complexes were characterized by IR, H-1 NMR and elementary analysis. Both 6 and 8 are still characterized by Sn-119 NMR. The molecular structure of 6 has been determined by X-ray diffraction. Crystals of 6 are orthorhombic, space group Pcab with a = 13.499(2) Angstrom, b = 16.883(6) Angstrom, c = 18.368(4) Angstrom, V = 4168(3) Angstrom(3), Z = 8, Dx = 2.044 g cm(-3), R (R-w)= 0.044 (0.059). (C) 1997 Elsevier Science S.A.
  • The first sila-bridged dicyclopentadienyl diruthenium complex: synthesis and X-ray structure of (Me2Si)[(η5-C5H4)Ru(CO)]2(μ-CO)2
    作者:Xiuzhong Zhou、Yongqiang Zhang、Shansheng Xu、Gonglu Tian、Baiquan Wang
    DOI:10.1016/s0020-1693(97)05505-9
    日期:1997.9
    Thermal treatment of a solution of Ru-3(CO)(12) and C5H5Me2SiC5H5 in heptane gives (Me2Si) [(eta(5)-C5H4)Ru(CO)](2)(mu-CO)(2) (1) in good yield. An investigation on the infrared spectra of 1 in KBr disc and CH2Cl2 solution reveals the coexistence of two isomers la (bridging form) and 1b (non-bridging form), with the former dominant. The molecular structure of 1a has been determined by X-ray diffraction.
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