p-tert-pentylsulfonylcalix[4]arene | 1609029-28-8

• 分子结构分类: 有机化合物
• 英文名称: p-tert-pentylsulfonylcalix[4]arene
• CAS: 1609029-28-8
• 化学式: C₄₄H₅₆O₁₂S₄
• 分子量: 905.185
• InChiKey: RGKZOHGYWZLZSF-UHFFFAOYSA-N

物化性质

• 沸点：
  1003.9±65.0 °C(predicted)
• 密度：
  1.321±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  8.9
• 重原子数：
  60.0
• 可旋转键数：
  8.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  217.48
• 氢给体数：
  4.0
• 氢受体数：
  12.0

反应信息

• 作为产物：
  描述：

  p-tert-pentylthiacalix[4]arene 在 sodium peroxoborate tetrahydrate 、 溶剂黄146 作用下， 以 氯仿 为溶剂， 反应 18.0h， 以90.6%的产率得到p-tert-pentylsulfonylcalix[4]arene
  参考文献：
  名称：

  Synthetic Supercontainers Exhibit Distinct Solution versus Solid State Guest-Binding Behavior

  摘要：

  The phase-dependent host-guest binding behavior of a new family of synthetic supercontainers has been probed in homogeneous solution and at liquid-liquid, solid-liquid, and solid-gas interfaces. The synthetic hosts, namely, type II metal-organic supercontainers (MOSCs), are constructed from the assembly of divalent metal ions, 1,4-benzenedicarboxylate (BDC) linker, and sulfonylcalix[4]arene-based container precursors. One member of the MOSCs, MOSC-II-tBu-Ni, which is derived from Ni(II), BDC, and p-tert-butylsulfonylcalix[4] arene (TBSC), crystallizes in the space group R (3) over bar and adopts pseudo face-centered cubic (fcc) packing, whereas other MOSCs, including TBSC analogue MOSC-II-tBu-Co, p-tert-pentylsulfonylcalix[4]arene (TPSC) analogues MOSC-II-tPen-Ni/Co, and p-tert-octylsulfonylcalix[4]arene (TOSC) analogues MOSC-II-tOc-Ni/Mg/Co, all crystallize in the space group I4/m and assume a pseudo body-centered cubic (bcc) packing mode. This solid-state structural diversity is nevertheless not reflected in their solution host-guest chemistry, as evidenced by the similar binding properties of MOSC-II-tBu-Ni and MOSC-II-tBu-Co in solution. Both MOSCs show comparable binding constants and adsorb ca. 7 equiv of methylene blue (MB) and ca. 30 equiv of aspirin in chloroform. In contrast, the guest-binding behavior of the MOSCs in solid state reveals much more variations. At the solid-liquid interface, MOSC-II-tBu-Co adsorb ca. S equiv of MB from an aqueous solution at a substantially faster rate than MOSC-II-tBu-Ni does. However, at the solid-gas interface, MOSC-II-tBu-Ni has higher gas uptake than MOSC-II-tBu-Co, contradicting their overall porosity inferred from the crystal structures. This discrepancy is attributed to the partial collapse of the solid-state packing of the MOSCs upon solvent evacuation. It is postulated that the degree of porosity collapse correlates with the molecular size of the MOSCs, i.e., the larger the MOSCs, the more severe they suffer from the loss of porosity. The same principle can rationalize the negligible N-2 and O-2 adsorption seen in the larger MOSC-II-tPen-Co and MOSC-II-tOC-Ni/Mg/Co molecules. MOSC-II-tPen-Ni features an intermediate molecular size and endures a partial structural collapse in such a way that the resulting pore dimension permits the inclusion of kinetically smaller O-2 (3.46 angstrom) but excludes larger N-2 (3.64 angstrom), explaining the observed remarkable O-2/N-2 adsorption selectivity.

  DOI：

  10.1021/ja502839b