1,3,5-triisobutyl-2,2,4,4,6,6-hexamethyl-1,3,5,2,4,6-triazatristanninane | 234443-33-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 三嗪烷类
• 英文名称: 1,3,5-triisobutyl-2,2,4,4,6,6-hexamethyl-1,3,5,2,4,6-triazatristanninane
• CAS: 234443-33-5
• 化学式: C₁₈H₄₅N₃Sn₃
• 分子量: 659.705
• InChiKey: KSIUFKMPAJWBLR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.98
• 重原子数：
  24.0
• 可旋转键数：
  6.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  9.72
• 氢给体数：
  0.0
• 氢受体数：
  3.0

反应信息

• 作为反应物：
  描述：

  1,3,5-triisobutyl-2,2,4,4,6,6-hexamethyl-1,3,5,2,4,6-triazatristanninane 、 三甲基铟 以 甲苯 为溶剂， 以100%的产率得到
  参考文献：
  名称：

  Synthese und Kristallstruktur voniso-Butylimidogalliummethyl, [CH3Ga-NCH2CH(CH3)2]6

  摘要：

  The thermal decomposition of [Me2Ga-N(Bu-i)SnMe3](2) (prepared by the reaction of [(Me2SnNBu)-Bu-i](3) with GaMe3 in a 1:3 molar ratio) in an evacuated, sealed tube at 160 degrees C forms [(MeGaNBu)-Bu-i](6) in high yield and SnMe4. Mass, H-1 and C-13 NMR as well as some IR and Raman spectroscopic data are given and the crystal structure of this cage molecule with a hexagonal prismatic Ga6N6 skeleton has been determined.

  DOI：

  10.1002/(sici)1521-3749(199902)625:2<186::aid-zaac186>3.0.co;2-v
• 作为产物：
  描述：

  二甲基二氯化锡 、 lithium isobutylamide 以 甲苯 为溶剂， 以65%的产率得到1,3,5-triisobutyl-2,2,4,4,6,6-hexamethyl-1,3,5,2,4,6-triazatristanninane
  参考文献：
  名称：

  Zur Reaktion voncyclo-Tristannazanen, [(CH3)2Sn-N(R)]3, mit den Trimethylderivaten des Aluminiums, Galliums und Indiums

  摘要：

  The cyclo-tristannazanes [Me2Sn-N(R)](3) (with R = Me, Pr-n,Pr-i,Bu-i) have been prepared from Me2SnCl2 and LiN(H)R in a 1:2 molar ratio. With MMe3 (M = Al, Ga, In) they form the dimeric dimethylmetal trimethylstannyl(alkyl)amides 1[Me2M-N(R)SnMe3](2) in good yields. The mass, NMR (H-1, C-13, Sn-119), and vibrational spectra are discussed and compared with the spectra of the tristannazanes. Thermolysis of the gallium amidocompounds splits SnMe4 to form methylgallium imido derivatives with cage structures. The crystal structures of selected stannylamido complexes have been determined by X-ray structure analysis.

  DOI：

  10.1002/(sici)1521-3749(199906)625:6<945::aid-zaac945>3.0.co;2-b