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[[[2-(dimethylamino)methyl]phenyl]silanediyl]iron(0) tetracarbonyl | 148538-96-9

中文名称
——
中文别名
——
英文名称
[[[2-(dimethylamino)methyl]phenyl]silanediyl]iron(0) tetracarbonyl
英文别名
{(2-(dimethylamino)methyl)phenylsilanediyl}iron(O) tetracarbonyl
[[[2-(dimethylamino)methyl]phenyl]silanediyl]iron(0) tetracarbonyl化学式
CAS
148538-96-9
化学式
C13H13FeNO4Si
mdl
——
分子量
331.183
InChiKey
DNBZDSCOYSXMAW-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:
    描述:
    五羰基铁2-[(dimethylamino)methyl]phenyltrihydrosilane正戊烷 为溶剂, 以81%的产率得到[[[2-(dimethylamino)methyl]phenyl]silanediyl]iron(0) tetracarbonyl
    参考文献:
    名称:
    Base Stabilization of Functionalized Silylene Transition Metal Complexes
    摘要:
    The dehydrogenative coupling reaction of primary silanes ArSiH3 [Ar = [2-(Me(2)NCH(2))C6H4], [8-(Me(2)NCH(2))C10H6], [8-(Me(2)N)C6H4]] with Fe(CO)(5), Cr(CO)(6), CpCo(CO)(2), and RCpMn(CO)(3) (R = H, CH3) under photolytic conditions affords an effective access to intramolecular base-stabilized functionalized silanediyl-transition metal complexes of general formula [ArHSi=MLn]. Si-29-NMR investigations of the photochemical reaction of PhSiH(3) with Fe(CO)(5) in the presence of 1,3-dimethyl-2-imidazolidinone (DMI) or hexamethylphosphoric triamide indicates a two-step mechanism for the formation of base-stabilized silanediyl-transition metal complexes. The carbonyl displacement reactions of the complex [2-(Me(2)-NCH2)C6H4]HSi=Cr(CO)(5) in the presence of PPh(3) or P(OMe)(3) lead to the formation of trans-(PPh(3))(2)Cr(CO)(4) or trans-[P(OMe)(3)]Cr-2(CO)(4), respectively, either by photolysis or by thermolysis. Photochemical displacement reaction with (diphenylphosphino)ethane furnished [2-(Me(2)NCH(2))C6H4]HSi=Cr[Ph(3)(CH2)(2)PPh(2)](CO)(3) by subsequent displacement of two carbonyls of the metal moiety. Exchange reactions of the complex [2-(Me(2)NCH(2))C6H4]HSi=Cr(CO)(5) with Ph(3)CX (X = Cl, BF4, OSO2CF3) or CH(3)COX' (X' = Cl, Pr) provide a direct entry to a series of functionalized complexes [2-(Me(2)NCH(2))C6H4]XSi=Cr(CO)(5). The liberated silylenes from complexes ArHSi(B)=Fe(CO)(4) (Ar = Ph, 1-Np) (B = DMI) can be trapped in the presence of tert-butyl alcohol or methanol to give di-tert-butoxysilanes or trimethoxysilanes, respectively.
    DOI:
    10.1021/om00004a019
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文献信息

  • Corriu, Robert J. P.; Lanneau, Gérard F.; Chauhan, Bhanu P. S., Organometallics, 1993, vol. 12, # 6, p. 2001 - 2003
    作者:Corriu, Robert J. P.、Lanneau, Gérard F.、Chauhan, Bhanu P. S.
    DOI:——
    日期:——
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