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2-Me2NC6H4NMg*THF | 269412-22-8

中文名称
——
中文别名
——
英文名称
2-Me2NC6H4NMg*THF
英文别名
——
2-Me2NC6H4NMg*THF化学式
CAS
269412-22-8
化学式
C4H8O*C8H10N2*Mg
mdl
——
分子量
230.593
InChiKey
OZDIUIQOMMKVRD-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):
    2.64
  • 重原子数:
    16.0
  • 可旋转键数:
    1.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    34.77
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

反应信息

  • 作为反应物:
    描述:
    三氯一茂钛2-Me2NC6H4NMg*THF甲苯 为溶剂, 以56%的产率得到[(η5-C5H5)Ti(Cl)(μ-NC6H4NMe2-2)]2
    参考文献:
    名称:
    Syntheses of titanium μ-arylimido and μ-pyridylimido complexes bearing (un)substituted cyclopentadienyl ligand
    摘要:
    The reactions of (eta(5)-C5H4CH2CH2Br)TiBr3, (eta(5)-C5H4CH2CH2OCH3)TiCl3, (eta(5)-C5H4-CH2-cyclo-C4H7O)TiCl3 and (eta(5)-C5H5)TiCl3 with an equivalent of 2-MeOC6H4NHLi in the presence of Et3N afford mu-arylimido complexes, [(eta(5)-C5H4CH2CH2Br)Ti(Br)(mu-NC6H4OCH3-2)](2) (1), [(eta(5)-C5H4CH2OCH3)Ti(Cl)(mu-NC6H4OCH3-2)](2) (2), [(eta(5)-C5H4-CH2-cyclo-C4H7O)Ti(Cl)(mu-NC6H4-OCH3-2)](2) (3), [(eta(5)-C5H5)Ti(Cl)(mu-NC6H4OCH3-2)](2) (4), which include intramolecular titanium and oxygen coordination. Complex 4 can also be obtained by reaction of the (eta(5)-C5H5)(2)TiCl2 with 2-MeOC6H4NHLi. Meanwhile refluxing of (eta 5-C5H5)(3)TiCl2 with an equivalent of 2-Me2NC6H4NMg.THF in toluene gives another mu-arylimido complex, [(eta(5)-C5H5)Ti(Cl)(mu-NC6H4NMe2-2)](2), which contains intramolecular titanium and nitrogen coordination. In addition, the analogous reactions of the above substituted half-sandwich Cp titanium complexes with PhNHLi in the presence of Et3N lead to [(eta(5)-C5H4CH2CH2Br)Ti(Br)(mu-NPh)](2), [(eta(5)-C5H4CH2OCH3)Ti(Cl)(mu-NPh)](2). The addition of 2-MeC6H4NHLi to (eta(5)-C5H4CH2CH2OCH3)TiCl3 and (eta(5)-C5H5)TiCl3 affords imido derivatives [(eta(5)-C5H5)Ti(Cl)(mu-NC6H4CH3-2)](2) and [(eta(5)-C5H4CH2OCH3)Ti(Cl)(mu-NC6H4CH3-2)](2). [(eta(5)-C5H5)Ti(Cl)(mu-NC6H3Me2-2,6)](2) is prepared by refluxing of (eta(5)-C5H5)TiCl3 and 2,6-Me2C6H3NMg.THF in toluene. The titanium mu-pyridylimido complexes, [(eta(5)-C5H5)Ti(Cl)(mu-NPy-2)](2), [(eta 5-C5H4CH2CH2OCH3)Ti(Cl)(mu-NPy-2)](2) and [(eta(5)-C5H4CH2CH2Br)Ti(Br)(mu-NPy-2)](2), are synthesized by reactions of the above corresponding half sandwich Cp titanium complexes with an equivalent of 2-PyNHLi in the presence of Et3N, respectively. Compound 1 crystallizes in the triclinic space group P (1) over bar (no. 2) with a = 9.942(2), b = 10.057(3), c = 8.457(2) Angstrom, alpha = 111.28(2), beta = 106.71(2), gamma = 98.12(2)degrees, V = 725.5(4) Angstrom(3), Z = 2.The catalytic activity and selectivity of compound 4 for the styrene polymerization is also investigated. (C) 2000 Elsevier Science S.A. All rights reserved.
    DOI:
    10.1016/s0022-328x(99)00732-9
  • 作为产物:
    描述:
    四氢呋喃N,N-二甲基邻苯二胺二丁基镁 作用下, 以 乙醚 为溶剂, 反应 12.0h, 以93%的产率得到2-Me2NC6H4NMg*THF
    参考文献:
    名称:
    Syntheses of titanium μ-arylimido and μ-pyridylimido complexes bearing (un)substituted cyclopentadienyl ligand
    摘要:
    The reactions of (eta(5)-C5H4CH2CH2Br)TiBr3, (eta(5)-C5H4CH2CH2OCH3)TiCl3, (eta(5)-C5H4-CH2-cyclo-C4H7O)TiCl3 and (eta(5)-C5H5)TiCl3 with an equivalent of 2-MeOC6H4NHLi in the presence of Et3N afford mu-arylimido complexes, [(eta(5)-C5H4CH2CH2Br)Ti(Br)(mu-NC6H4OCH3-2)](2) (1), [(eta(5)-C5H4CH2OCH3)Ti(Cl)(mu-NC6H4OCH3-2)](2) (2), [(eta(5)-C5H4-CH2-cyclo-C4H7O)Ti(Cl)(mu-NC6H4-OCH3-2)](2) (3), [(eta(5)-C5H5)Ti(Cl)(mu-NC6H4OCH3-2)](2) (4), which include intramolecular titanium and oxygen coordination. Complex 4 can also be obtained by reaction of the (eta(5)-C5H5)(2)TiCl2 with 2-MeOC6H4NHLi. Meanwhile refluxing of (eta 5-C5H5)(3)TiCl2 with an equivalent of 2-Me2NC6H4NMg.THF in toluene gives another mu-arylimido complex, [(eta(5)-C5H5)Ti(Cl)(mu-NC6H4NMe2-2)](2), which contains intramolecular titanium and nitrogen coordination. In addition, the analogous reactions of the above substituted half-sandwich Cp titanium complexes with PhNHLi in the presence of Et3N lead to [(eta(5)-C5H4CH2CH2Br)Ti(Br)(mu-NPh)](2), [(eta(5)-C5H4CH2OCH3)Ti(Cl)(mu-NPh)](2). The addition of 2-MeC6H4NHLi to (eta(5)-C5H4CH2CH2OCH3)TiCl3 and (eta(5)-C5H5)TiCl3 affords imido derivatives [(eta(5)-C5H5)Ti(Cl)(mu-NC6H4CH3-2)](2) and [(eta(5)-C5H4CH2OCH3)Ti(Cl)(mu-NC6H4CH3-2)](2). [(eta(5)-C5H5)Ti(Cl)(mu-NC6H3Me2-2,6)](2) is prepared by refluxing of (eta(5)-C5H5)TiCl3 and 2,6-Me2C6H3NMg.THF in toluene. The titanium mu-pyridylimido complexes, [(eta(5)-C5H5)Ti(Cl)(mu-NPy-2)](2), [(eta 5-C5H4CH2CH2OCH3)Ti(Cl)(mu-NPy-2)](2) and [(eta(5)-C5H4CH2CH2Br)Ti(Br)(mu-NPy-2)](2), are synthesized by reactions of the above corresponding half sandwich Cp titanium complexes with an equivalent of 2-PyNHLi in the presence of Et3N, respectively. Compound 1 crystallizes in the triclinic space group P (1) over bar (no. 2) with a = 9.942(2), b = 10.057(3), c = 8.457(2) Angstrom, alpha = 111.28(2), beta = 106.71(2), gamma = 98.12(2)degrees, V = 725.5(4) Angstrom(3), Z = 2.The catalytic activity and selectivity of compound 4 for the styrene polymerization is also investigated. (C) 2000 Elsevier Science S.A. All rights reserved.
    DOI:
    10.1016/s0022-328x(99)00732-9
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