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(η3-tetraglyme)CaCp2 | 1272031-21-6

中文名称
——
中文别名
——
英文名称
(η3-tetraglyme)CaCp2
英文别名
calcium;cyclopenta-1,3-diene;1-methoxy-2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethane
(η3-tetraglyme)CaCp2化学式
CAS
1272031-21-6
化学式
C20H32CaO5
mdl
——
分子量
392.549
InChiKey
JXMFJEQGLLYQID-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):
    2.76
  • 重原子数:
    26
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    46.2
  • 氢给体数:
    0
  • 氢受体数:
    7

反应信息

  • 作为产物:
    描述:
    四乙二醇二甲醚bis(thf) calcocene四氢呋喃 为溶剂, 以58.1%的产率得到(η3-tetraglyme)CaCp2
    参考文献:
    名称:
    Coordination Behavior of Calcocene and Its Use as a Synthon for Heteroleptic Organocalcium Compounds
    摘要:
    The insoluble calcocene Ca(eta(5)-C5H5)(2) readily dissolves after addition of Lewis bases. Monodentate donor solvents such as tetrahydrofuran (thf), pyridine (py), and tetrahydropyran (thp) forrn complexes of the type [(L)(2)CaCp2] (L = thf (1), py (2), thp (4)). Bidentate Lewis bases such as 1,2-bis(dimethylamino)ethane (tmeda) and 1,2-dimethoxyethane (dme) act as chelating ligands in complexes of the type [(L)CaCp2] (L = tmeda (3), dme (5)). Multidentate ether of the type MeO-(CH2CH2O)(n)-Me (n = 2, diglyme; n = 3, triglyme; n = 4, tetraglyme) bind in all cases as tridentate Lewis bases of the type [(eta(3)-L)CaCp2] (L = diglyme (6), triglyme (7), tetraglyme (8)), but the formation of [(L)CaCp](+) cations with these ethers or even with crown ilathers was not observed. However, partial hydrolysis of 1 releases one Cp ligand, and from this reaction mixture crystalline [(15C5)CaCp](+)[(thf)CaCp3](-) (9) precipitates in the.presence of 15-crown-5 (15C5). Calcocene behaves as a pseudohalide complex of calcium, and of 1 or 5 with phenyllithium in the presence of DME yields heteroleptic [(dme)(eta(5)-Cp)Ca(mu-Ph)](2) (10), which forms a diner with bridging phenyl groups in the solid state. Especially this last reaction offers an expansion of organocalcium chemistry.
    DOI:
    10.1021/om100806f
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