1,3-di(tert-butyl)-2,2-dimethyl-1,3,2,4-diazasilastannetidine-4-spiro-2'-1,3-di-p-tolyl-1,3,2,4-diazadistannetidine-4'-spiro-4''-{1,3-di(tert-butyl)-2,2-dimethyl-1,3,2,4-diazasilastannetidine} | 155998-64-4

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 1,3-di(tert-butyl)-2,2-dimethyl-1,3,2,4-diazasilastannetidine-4-spiro-2'-1,3-di-p-tolyl-1,3,2,4-diazadistannetidine-4'-spiro-4''-{1,3-di(tert-butyl)-2,2-dimethyl-1,3,2,4-diazasilastannetidine}
• 英文别名: 1,3,7,9-tetratert-butyl-2,2,8,8-tetramethyl-5,10-bis(4-methylphenyl)-1,3,5,7,9,10-hexaza-2,8-disila-4,6-distannadispiro[3.1.36.14]decane
• CAS: 155998-64-4
• 化学式: C₃₄H₆₂N₆Si₂Sn₂
• 分子量: 848.497
• InChiKey: NBRMVORQUIWELE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  8.33
• 重原子数：
  44.0
• 可旋转键数：
  2.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.65
• 拓扑面积：
  19.44
• 氢给体数：
  0.0
• 氢受体数：
  6.0

反应信息

• 作为产物：
  描述：

  p-叠氮甲苯 、 1,3-di-t-butyl-2,2-dimethyl-1,3,2,4λ2-diazasilastannetidine 以 四氢呋喃 为溶剂， 生成 1,3-di(tert-butyl)-2,2-dimethyl-1,3,2,4-diazasilastannetidine-4-spiro-2'-1,3-di-p-tolyl-1,3,2,4-diazadistannetidine-4'-spiro-4''-{1,3-di(tert-butyl)-2,2-dimethyl-1,3,2,4-diazasilastannetidine}
  参考文献：
  名称：

  Khmaruk, A. M.; Oleinik, V. A.; Kasukhin, L. F., Journal of general chemistry of the USSR, 1987, vol. 57, p. 980 - 984

  摘要：

  DOI：

文献信息

• Chemie der schweren Carben-Analogen R2M (M  Si, Ge, Sn) XIX . Reaktionen von stabilem Diaminogermylen und -stannylen Me2Si(tBuN)2 M (M  Ge, Sn) mit organischen Aziden
  作者：Beatrix Klein、Wilhelm P. Neumann

  DOI：10.1016/0022-328x(94)87045-4

  日期：1994.2

  The reaction of Veith's germylene Me(2)Si((t)BuN)(2)Ge 1 with an excess of organic azides R-N-3 2a-2i under elimination of N-2, very probably gives the unstable, reactive germaimines Me(2)Si((t)BuN)(2)Ge=N-R that dimerize rapidly even at -40 degrees C, yielding the dispirodecanes 4a-4g. At higher temperatures, however, the [2 + 3] dipolar cycle-addition of a second molecule of R-N-3 leading to 5-germa tetrazolines, 3a-3e, competes successfully. This depends on the nature of R, and is thermally reversible. Other scavengers are, e.g. Me(3)Sn-Cl or Me(3)Si-N-3. With the corresponding Veith-stannylene 5, only dispiro compounds 4h-4k are obtained, and no 5-stanna tetrazoline. 1 and 5 exhibit, however, the same activity toward p-tolyl azide, leading, in a competitive experiment, to a statistical 1:1:2 distribution of the Ge-2, Sn-2, and Ge, Sn (41) dispirodecanes. The stability of the tricyclic system 4 in most of the examples is very high. Thus, in the mass spectra of 4b, 4k, 4l the molecular peaks M(+) (m/z = 756, 848, 802) are the respective base peaks, followed by (M-Me)(+). Doubly loaded ions (M-2Me)(2+) are also surprisingly stable. Most of the obtained compounds are new.
• XMARUK A. M.; OLEJNIK V. A.; KASUXIN L. F.; PONOMARCHUK M. P.; PINCHUK A.+, ZH. OBSHCH. XIMII, 57,(1987) N 5, 1097-1102
  作者：XMARUK A. M.、 OLEJNIK V. A.、 KASUXIN L. F.、 PONOMARCHUK M. P.、 PINCHUK A.+

  DOI：——

  日期：——