[8-[(dimethylamino)methyl]naphtyl]-1-phenyldihydrosilane | 106586-06-5

• 英文名称: [8-[(dimethylamino)methyl]naphtyl]-1-phenyldihydrosilane
• CAS: 106586-06-5
• 化学式: C₁₉H₂₁NSi
• 分子量: 291.468
• InChiKey: MOLLXXGJVSWWGH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  None
• 重原子数：
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• 可旋转键数：
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• 环数：
  None
• sp3杂化的碳原子比例：
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• 拓扑面积：
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• 氢给体数：
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• 氢受体数：
  None

反应信息

• 作为反应物：
  描述：

  [8-[(dimethylamino)methyl]naphtyl]-1-phenyldihydrosilane 在 selenium 作用下， 以 氘代氯仿 为溶剂， 反应 0.5h， 以84%的产率得到2,2-dimethyl-1-phenyl-2,3-dihydro-1H-1l5,2l4-naphtho[1,8-cd][1,2]azasiline-1-selenone
  参考文献：
  名称：

  Arya, Prabhat; Boyer, Jacqueline; Carre, Francis, Angewandte Chemie, 1989, vol. 101, # 8, p. 1069 - 1071

  摘要：

  DOI：

文献信息

• Corriu, Robert; Lanneau, Gerard; Priou, Christian, Angewandte Chemie, 1991, vol. 103, # 9, p. 1153 - 1155
  作者：Corriu, Robert、Lanneau, Gerard、Priou, Christian

  DOI：——

  日期：——
• Lewis Base-Stabilized Transition Metal Complexes of Divalent Silicon Species
  作者：Bhanu P. S. Chauhan、Robert J. P. Corriu、Gerard F. Lanneau、Christian Priou、Norbert Auner、Hermann Handwerker、Eberhardt Herdtweck

  DOI：10.1021/om00004a020

  日期：1995.4

  A direct photochemical synthesis of silanediyl-iron tetracarbonyl complexes Ph(2)Si(B)=Fe-(CO)(4) [B = 1,3-dimethylimidazolidinone (DMI) or hexamethylphosphoric triamide (HMPA)] is described. The Lewis base character of DMI is strong enough to quantitatively convert the dimeric [Fe-2(CO)(8)(SiPh(2))(2)] to more stable Ph(2)Si(DMI)=Fe(CO)(4). A series of organosilanediyl-transition metal complexes, of general formula ArAr'Si=MLn [Ar = Ph, Ar' = [2-(Me(2)NCH(2))C6H4], [8-(Me(2)NCH(2))C10H6], [8-(Me(2)N)C10H6]; Ar, Ar' = [2-(Me(2)NCH(2))C6H4]; Ar = 1-Np, Ar' = [8-(Me(2)NCH(2))C10H6]; or Ar = Me, Ar' = [2-(Me(2)NCH(2))C6H4]] is directly obtained in the photochemical reaction of ArAr'SiH2 with Fe(CO)(5), Cr(CO)(6), Mo(CO)(6), and RCpMn(CO)(3) (R = Me, H). Single-crystal X-ray structure analysis of the complex [2-(Me(2)NCH(2))C6H4]C6H5Si = Fe(CO)(4) (5a) reveals a N-->Si bond length of 1.962(2)Angstrom and Si-Fe bond distance of 2.259(1)Angstrom. The sum of bond angles at silicon, excluding the N-atom, is to 346.7 degrees. Crystal data: C19H17FeNO4Si, triclinic, space group P1 (No. 2), a = 8.284(2), b = 8.404(2), c = 13.497(3)Angstrom; alpha = 97.02(1)degrees, beta = 93.68(1)degrees, gamma = 91.25(1)degrees, V = 930.3 Angstrom(3), Z = 2, R = 0.027, R omega = 0.030 based on 3171 reflections with (I > 0.00, all data). Strong intramolecular donor stabilization with the 8-[(dimethylamino)methyl]naphthyl ligand directly bonded to the silicon atom prevents further reactions, but typical experiments have been performed with less coordinated 8-[(dimethylamino)methyl]phenyl derivatives. Silanediyl-iron tetracarbonyl complexes react with acetylenes, dienes, and alcohols under UV irradiation, and trapping products of silylenes are isolated in good yields. A comparative study of different coordinating ligands has been carried out.
• Enhancement of SiH bond reactivity in pentacoordinated structures
  作者：J. Boyer、C. Breliere、R.J.P. Corriu、A. Kpoton、M. Poirier、G. Royo

  DOI：10.1016/0022-328x(86)80263-7

  日期：1986.9