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[Me2Si(NCMe3)(OCMe3)]2Y(NC5H6) | 199462-39-0

中文名称
——
中文别名
——
英文名称
[Me2Si(NCMe3)(OCMe3)]2Y(NC5H6)
英文别名
——
[Me2Si(NCMe3)(OCMe3)]2Y(NC5H6)化学式
CAS
199462-39-0
化学式
C25H54N3O2Si2Y
mdl
——
分子量
573.8
InChiKey
JUFOUJGABCPHTI-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):
    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

  • 作为产物:
    参考文献:
    名称:
    Synthesis and Reactivity of Bis(alkoxysilylamido)yttrium η2-Pyridyl and η2-α-Picolyl Compounds
    摘要:
    The synthesis and reactivity of bis(alkoxysilylamido)yttrium pyridyl and alpha-picolyl complexes [Me2Si(NCMe3)(OCMe3)](2) YR (R=eta(2)-(C,N)-2-NC5H4(1); R=eta(2)(C,N)-CH2-2-NC5H4 (2); R=eta(2)-(C,N)-C(H)Me-2-NC5H4 (3); R=eta(2)-(C,N)-C(H)Me-2-NC5H3-6-Me (4)) is reported 1-4 have been prepared by C-H activation of pyridine and the corresponding methyl (ethyl) and dimethyl-substituted pyridines from [Me2Si(NCMe3)(OCMe3)](2)YCH(SiMe3)(2) and by salt metathesis with the appropriate lithium salts from [Me2Si(NCMe3)(OCMe3)](2) YCl . THF. The molecular structure of 2 shows that the picolyl group is bonded to yttrium in an eta(3)-aza-allylic fashion. With dihydrogen, stepwise hydrogenation of the pyridyl fragment of 1 has been observed, finally yielding the 2,3-dihydropyridyl complex [Me2Si(NCMe3)(OCMe3)](2)YNC5H8(7). Compound 1 inserts ethene to form the alpha-methylpicolyl derivative 4. Polymerization of ethene was not observed. The pyridyl compound 1 reacts with PhC drop CH to yield the corresponding acetylide pyridine complex [Me2Si(NCMe3)(OCMe3)](2) YC drop CPh . Py (8). The complexed pyridine can be substituted by THF to give [Me2Si(NCMe3)(OCMe3)](2) YC drop CPh . THF (9), which easily loses THF and forms the base-free acetylide [Me2Si(NCMe3)(OCMe3)](2) YC drop CPh (10). Compounds 1 and 2 readily insert nitriles yielding imido-pyridine complexes. The imido-pyridine complexes that contain alpha-hydrogen readily undergo a 1,3-H shift affording the corresponding enamido-pyridine compounds. With CO, the pyridyl compound 1 gives a dipyridylketone complex {[Me2Si(NCMe3)(OCMe3)](2) Y}{mu,eta(2),eta(2)-(N,N',O)-OC(2-NC5H4)(2)} (15).
    DOI:
    10.1021/om970540d
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