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(2-P,P-dimethylphosphanylethyl)-tetramethylcyclopentadiene

中文名称
——
中文别名
——
英文名称
(2-P,P-dimethylphosphanylethyl)-tetramethylcyclopentadiene
英文别名
Phosphine, dimethyl[2-(2,3,4,5-tetramethyl-1,4-cyclopentadien-1-yl)ethyl]-;dimethyl-[2-(2,3,4,5-tetramethylcyclopenta-1,4-dien-1-yl)ethyl]phosphane
(2-P,P-dimethylphosphanylethyl)-tetramethylcyclopentadiene化学式
CAS
——
化学式
C13H23P
mdl
——
分子量
210.299
InChiKey
HAOLMZANBHPVDS-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):
    1.5
  • 重原子数:
    14
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.69
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为产物:
    描述:
    sodium (2-P,P-dimethylphosphanylethyl)tetramethylcyclopentadienide 在 甲醇 作用下, 生成 (2-P,P-dimethylphosphanylethyl)-tetramethylcyclopentadiene 、 (2-P,P-dimethylphosphanylethyl)-tetramethylcyclopentadiene 、 (2-P,P-dimethylphosphanylethyl)-tetramethylcyclopentadiene
    参考文献:
    名称:
    Mono- and bis-[2-(P,P-dimethylphosphanyl)ethyl]tetramethylcyclopentadienyl zirconium(IV) complexes: Synthesis and structural studies in crystalline state and in solutions
    摘要:
    Synthetic routines for a new ligand C5Me4CH2CH2PMe2 (2b) in forms of its Li- (2b-Li), Na- (2b-Na) salts and in the CH-form (2b-H), as well as for silanes Me3Si-C5H4CH2CH2PMe2 (3a) and Me3Si-C5Me4CH2CH2PMe2 (3b) have been developed. On the basis of it, new half-sandwich [eta(5) :eta(1)-kappa P-C5H4CH2CH2PMe2]ZrCl3 (4a), [eta(5):eta(1)-kappa P-C5Me4CH2CH2PMe2]ZrCl3 (4b) and sandwich [eta(5)-C5Me4CH2CH2PMe2](2)ZrCl2 (5), [eta(5)-C5Me4CH2CH2PMe2][eta(5)-C5Me5]ZrCl3 (6) complexes of Zr(IV) have been prepared and characterized. Along with them, the first example of X-ray structurally characterized dinuclear Zr(IV) complex incorporating both sandwich (6) and half-sandwich (4b) moieties linked one to another by means of Zr P coordination bond 7, has been described. Formation of an analogously organized trinuclear complex 8, built from one sandwich fragment of 5 and two half-sandwich fragments of 4b was proved by NMR spectroscopy methods. Molecular structures of half-sandwich complexes in their solvent-free dimeric forms (4a and 4b) and as 1: 1 adducts with THF (4a-THF and 4b-THF) along with those of dinuclear complex 7 have been established by X-ray diffraction analyses. The dynamic behavior for di- and trinuclear complexes 7 and 8, due to the intermolecular dissociation-coordination of the Me2P-groups in THF-d(8) solutions has been studied by variable-temperature NMR spectroscopy. (c) 2005 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2005.06.008
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