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Ti(η5-C5H5)2(SC2H5)2 | 1291-79-8

中文名称
——
中文别名
——
英文名称
Ti(η5-C5H5)2(SC2H5)2
英文别名
——
Ti(η5-C5H5)2(SC2H5)2化学式
CAS
1291-79-8
化学式
C14H20S2Ti
mdl
——
分子量
300.325
InChiKey
FFGFOPSUAKWRDL-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:
    tetrakis(actonitrile)copper(I) hexafluorophosphate 、 Ti(η5-C5H5)2(SC2H5)2 在 C5H5N 作用下, 以 四氢呋喃 为溶剂, 生成
    参考文献:
    名称:
    Wark, Teresa A.; Stephan, Douglas W., Inorganic Chemistry, 1987, vol. 26, # 3, p. 363 - 369
    摘要:
    DOI:
  • 作为产物:
    描述:
    二氯二茂钛乙硫醇 在 (C2H5)3N 作用下, 以 为溶剂, 生成 Ti(η5-C5H5)2(SC2H5)2
    参考文献:
    名称:
    Wark, Teresa A.; Stephan, Douglas W., Inorganic Chemistry, 1987, vol. 26, # 3, p. 363 - 369
    摘要:
    DOI:
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文献信息

  • Photochemistry and electronic structure of the bis(.eta.5-cyclopentadienyl)titanium sulfide [(.eta.5-C5H5)2TiS5] complex
    作者:Alice E. Bruce、Mitchell R. M. Bruce、David R. Tyler
    DOI:10.1021/ja00334a033
    日期:1984.10
  • Thiolato Ligand Transfer from Bis(thiolato)titanocenes to Platinum(II) Complexes
    作者:Kohtaro Osakada、Yasuharu Kawaguchi、Takakazu Yamamoto
    DOI:10.1021/om00010a019
    日期:1995.10
    Reactions of Cp(2)Ti(SEt)(2) (la) and Cp(2)Ti(S-i-Pr)(2) (Ib) with equimolar PtCl2(cod)(2) give bis(thiolato)platinum complexes, [Pt(SEt)(2)](n), (2a) and [Pt(S-i-Pr)(2)](n) (2b), respectively, accompanied by formation of Cp(2)TiCl(2). Complexes 2a,b, which are insoluble in common organic solvents, are characterized by elemental analyses and by CP-MAS C-13 NMR spectra in the solid state. Cp(2)Ti(SC6H4-p-Me)(2) (Ic), Cp(2)Ti(SPh)(2) (Id), Cp(2)Ti(S2C6H4) (le), and Cp(2)Ti(S2C2H4) (If) react with equimolar PtCl2(cod) smoothly to give mixtures of Cp(2)TiCl(2) and (thiolato)platinum complexes with the cod Ligand, Pt(SC6H4-p-Me)(2)(cod) (3c), Pt(SPh)(2)(cod) (3d), Pt(S2C6H4)(cod) (3e), and Pt(S2C2H4)(cod) (3f), respectively. Reactions of la with excess PtCl2(cod) in THF and in CH2Cl2 cause a color change of the solution indicating initial. formation of Cp(2)TiCl(SEt) followed by its further reaction with Pt complexes to give Cp(2)TiCl(2). The latter step, which is much slower than the former, obeys pseudo-first-order kinetics with respect to [Cp(2)TiCl(SEt)], The observed rate constants, k(obsd), of the reaction in CH2Cl2 are proportional to [PtCl2(cod)]. Temperature dependence of the rate constants in THF gives the kinetic parameters E(a) = 57.4 kJ mol(-1), Delta H double dagger = 54.8 kJ mol(-1), Delta S double dagger = -106 J mol(-1) K-1, and Delta G double dagger = 86.3 kJ mol(-1) at 298 K. Reaction of 1b with excess PtCl2(cod) also gives Cp(2)TiCl(2) through Cp(2)TiCl(S-i-Pr). The kinetic parameters of the reaction are E(a) = 62.3 kJ mol(-1), Delta H double dagger = 59.8 kJ mol(-1), Delta S double dagger = -124 J mol(-1) K-1, and Delta G double dagger = 96.7 kJ mol(-1) at 298 K. The absorption spectrum of a reaction mixture of If with excess PtCl2(cod) shows a decrease in the peak due to If with concomitant growth of a peak due to Cp(2)TiCl(2). The reaction obeys 0.5th-order kinetics with respect to [1f]. Reactions of Ic,d with equimolar PtCl2(cod) in toluene give the complexes formulated as [Cp(2)Ti(SAr)(2)PtCl2(cod)] (4c, Ar = C6H4-p-Me; 4d, Ar = Ph), which are characterized by elemental analyses and C-13 NMR spectra in the solid state. Dissolution of 4c,d in THF causes formation of a mixture of Cp(2)TiCl(2) with 3c,d, respectively.
  • Wark, Teresa A.; Stephan, Douglas W., Inorganic Chemistry, 1990, vol. 29, # 9, p. 1731 - 1736
    作者:Wark, Teresa A.、Stephan, Douglas W.
    DOI:——
    日期:——
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