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[(η(5)-C5Me5)Ru(CH2CH2Ph)(μ-SPr(i))2Ru(η(5)-C5Me5)(CH2CH2Ph)] | 167495-23-0

中文名称
——
中文别名
——
英文名称
[(η(5)-C5Me5)Ru(CH2CH2Ph)(μ-SPr(i))2Ru(η(5)-C5Me5)(CH2CH2Ph)]
英文别名
ethylbenzene;1,2,3,4,5-pentamethylcyclopenta-1,3-diene;propane-2-thiolate;ruthenium(3+)
[(η(5)-C5Me5)Ru(CH2CH2Ph)(μ-SPr(i))2Ru(η(5)-C5Me5)(CH2CH2Ph)]化学式
CAS
167495-23-0
化学式
C42H62Ru2S2
mdl
——
分子量
833.226
InChiKey
PVNPJNSELYCOFG-UHFFFAOYSA-L
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:
    [(η(5)-C5Me5)Ru(CH2CH2Ph)(μ-SPr(i))2Ru(η(5)-C5Me5)(CH2CH2Ph)]四氢呋喃 为溶剂, 以46%的产率得到[(η(5)-C5Me5)RuI(μ-SPr(i))2Ru(η(5)-C5Me5)I]
    参考文献:
    名称:
    Syntheses and characterization of diruthenium(III) alkyl-alkyl and alkyl-alkynyl complexes with two bridging thiolate ligands . X-ray structure of [Cp∗Ru(CH2CH2Ph)(μ-SPri)2RuCp∗(CH2CH2Ph)]
    摘要:
    Reactions of diruthenium alkyl-halido complexes containing two bridging thiolate ligands [Cp*RuR(mu-SPri)(2)RuCp*X](1; Cp* = eta(5)-C(5)Me(5), R = PhCH(2)CH(2), X = Br, R = Me, X = I) with R'MgX(R' = PhCH(2)CH(2), X = Br; R' = PhCH(2), X = Cl) or R'Li(R'= Me, PhC = C) in THF at room temperature afforded novel diruthenium alkyl-alkyl and alkyl-alkynyl complexes [Cp*RuR(mu-SPri)(2)RuCp*R'] (2). In contrast, treatment of 1a (R = PhCH(2)CH(2), X = Br) with EtMgBr resulted in the formation of an alkyl-hydrido complex [Cp*Ru(CH(2)CH(2)Ph)(mu-SPri)(2)RuCp*H] as the only isolable product. X-ray analysis of 2a (R = R'= PhCH(2)CH(2)) has disclosed the structure as consisting of the two Cp*Ru(CH(2)CH(2)Ph) units connected by two mu-SPri ligands together with a Ru-Ru single bond, in which the two alkyl groups are oriented mutually cis. Crystal data for 2a: monoclinic, space group P2(1)/c(No. 14) with a = 19.449(3) Angstrom, b = 10.210(3) Angstrom, c = 20.254(2) Angstrom, beta = 94.684(9)degrees, V = 4008(2) Angstrom(3), Z = 4, and R(R(W)) = 0.054 (0.041) for 2635 reflections [I > 3 sigma(I)]. Treatment of 2a with two equivalents of I-2 in THF resulted in the formation of PhCH(2)CH(2)I and [Cp*RuI(mu-SPri)(2)RuCp*I] (7c) as the major products, while treatment with 1.2 equivalents of I-2 afforded a mixture of Ph(CH2)(4)Ph and PhCH(2)CH(2)I along with 7e and unidentified Ru species.
    DOI:
    10.1016/0022-328x(95)05477-7
  • 作为产物:
    描述:
    magnesium,ethylbenzene,bromide 、 [(η(5)-C5Me5)Ru(CH2CH2Ph)(μ-SPr(i))2Ru(η(5)-C5Me5)Br] 以 四氢呋喃 为溶剂, 以34%的产率得到[(η(5)-C5Me5)Ru(CH2CH2Ph)(μ-SPr(i))2Ru(η(5)-C5Me5)(CH2CH2Ph)]
    参考文献:
    名称:
    Syntheses and characterization of diruthenium(III) alkyl-alkyl and alkyl-alkynyl complexes with two bridging thiolate ligands . X-ray structure of [Cp∗Ru(CH2CH2Ph)(μ-SPri)2RuCp∗(CH2CH2Ph)]
    摘要:
    Reactions of diruthenium alkyl-halido complexes containing two bridging thiolate ligands [Cp*RuR(mu-SPri)(2)RuCp*X](1; Cp* = eta(5)-C(5)Me(5), R = PhCH(2)CH(2), X = Br, R = Me, X = I) with R'MgX(R' = PhCH(2)CH(2), X = Br; R' = PhCH(2), X = Cl) or R'Li(R'= Me, PhC = C) in THF at room temperature afforded novel diruthenium alkyl-alkyl and alkyl-alkynyl complexes [Cp*RuR(mu-SPri)(2)RuCp*R'] (2). In contrast, treatment of 1a (R = PhCH(2)CH(2), X = Br) with EtMgBr resulted in the formation of an alkyl-hydrido complex [Cp*Ru(CH(2)CH(2)Ph)(mu-SPri)(2)RuCp*H] as the only isolable product. X-ray analysis of 2a (R = R'= PhCH(2)CH(2)) has disclosed the structure as consisting of the two Cp*Ru(CH(2)CH(2)Ph) units connected by two mu-SPri ligands together with a Ru-Ru single bond, in which the two alkyl groups are oriented mutually cis. Crystal data for 2a: monoclinic, space group P2(1)/c(No. 14) with a = 19.449(3) Angstrom, b = 10.210(3) Angstrom, c = 20.254(2) Angstrom, beta = 94.684(9)degrees, V = 4008(2) Angstrom(3), Z = 4, and R(R(W)) = 0.054 (0.041) for 2635 reflections [I > 3 sigma(I)]. Treatment of 2a with two equivalents of I-2 in THF resulted in the formation of PhCH(2)CH(2)I and [Cp*RuI(mu-SPri)(2)RuCp*I] (7c) as the major products, while treatment with 1.2 equivalents of I-2 afforded a mixture of Ph(CH2)(4)Ph and PhCH(2)CH(2)I along with 7e and unidentified Ru species.
    DOI:
    10.1016/0022-328x(95)05477-7
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