2,11,20,29,37,38,39,40-Octazanonacyclo[28.6.1.13,10.112,19.121,28.04,9.013,18.022,27.031,36]tetraconta-1,3,5,7,9,11,13(18),14,16,19(39),20,22(27),23,25,28,30(37),31(36),32,34-nonadecaene-6,15,24,33-tetracarboxylic acid

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 四吡咯及其衍生物
• 英文名称: 2,11,20,29,37,38,39,40-Octazanonacyclo[28.6.1.13,10.112,19.121,28.04,9.013,18.022,27.031,36]tetraconta-1,3,5,7,9,11,13(18),14,16,19(39),20,22(27),23,25,28,30(37),31(36),32,34-nonadecaene-6,15,24,33-tetracarboxylic acid
• 英文别名: 2,11,20,29,37,38,39,40-octazanonacyclo[28.6.1.13,10.112,19.121,28.04,9.013,18.022,27.031,36]tetraconta-1,3,5,7,9,11,13(18),14,16,19(39),20,22(27),23,25,28,30(37),31(36),32,34-nonadecaene-6,15,24,33-tetracarboxylic acid
• 化学式: C₃₆H₁₈N₈O₈
• 分子量: 690.588
• InChiKey: BXCQAKXPAYQXGF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.5
• 重原子数：
  52
• 可旋转键数：
  4
• 环数：
  9.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  258
• 氢给体数：
  6
• 氢受体数：
  14

反应信息

• 作为产物：
  描述：

  2,11,20,29,37,38,39,40-Octazanonacyclo[28.6.1.13,10.112,19.121,28.04,9.013,18.022,27.031,36]tetraconta-1,3,5,7,9,11,13(18),14,16,19(39),20,22(27),23,25,28,30(37),31(36),32,34-nonadecaene-6,15,24,33-tetracarboxamide 在 硫酸 、 sodium nitrite 作用下， 反应 1.0h， 以26.9%的产率得到2,11,20,29,37,38,39,40-Octazanonacyclo[28.6.1.13,10.112,19.121,28.04,9.013,18.022,27.031,36]tetraconta-1,3,5,7,9,11,13(18),14,16,19(39),20,22(27),23,25,28,30(37),31(36),32,34-nonadecaene-6,15,24,33-tetracarboxylic acid
  参考文献：
  名称：

  可溶性无金属/金属酞菁四羧酸的改进合成及其在环己烯催化环氧化中的应用

  摘要：

  摘要 使用基于重氮反应改进水解的新方法合成了不含可溶性金属和金属（铜 (II)、铁 (III) 和钴 (II)）酞菁四羧酸 (5-8)。所得化合物（5-8）通过 X 射线衍射、紫外-可见光谱和 FT-IR 光谱表征，然后用作催化剂以分子氧为氧化剂进行环己烯的环氧化。优化反应条件，包括反应时间、温度、催化剂用量和异丁醛/环己烯比，以实现最高的氧化环己烯选择性。比较了不含金属的酞菁四羧酸 (5) 和金属（铜 (II)、铁 (III) 和钴 (II)）酞菁四羧酸（分别为 6–8）。配合物6-8在最佳条件下表现出比化合物5更高的催化活性。图文摘要采用新方法合成了四种可溶性无金属和金属PTCs，并将其用作环己烯环氧化反应的催化剂，分子氧为氧化剂。在最佳条件下，共实现了58.1%的氧化环己烯选择性和收率。

  DOI：

  10.1007/s10562-015-1500-0

文献信息

• Organic dye, photoelectric transducing material, semiconductor electrode, and photoelectric transducing device
  申请人：Mitsubishi Paper Mills Limited

  公开号：EP1997855A2

  公开（公告）日：2008-12-03

  Disclosed are an organic dye having a specific structure, a photoelectric conversion material containing the dye, a semiconductor electrode formed of a substrate having an electrically conductive surface, a semiconductor layer coated on the electrically conductive surface and the above dye adsorbed on the surface, and a photoelectric conversion device to which the above dye is applied. The present invention uses the above dye and can therefore provide a photoelectric conversion device excellent in photoelectric conversion efficiency, and the photoelectric conversion device is suitable for use in a solar cell or the like.

  本发明公开了一种具有特定结构的有机染料，一种含有该染料的光电转换材料，一种由具有导电表面的基板、涂覆在导电表面上的半导体层和吸附在该表面上的上述染料构成的半导体电极，以及一种应用了上述染料的光电转换装置。 本发明使用了上述染料，因此可以提供一种光电转换效率极佳的光电转换装置，该光电转换装置适用于太阳能电池等。
• ORGANIC DYE, PHOTOELECTRIC TRANSDUCING MATERIAL, SEMICONDUCTOR ELECTRODE, AND PHOTOELECTRIC TRANSDUCING DEVICE
  申请人：MITSUBISHI PAPER MILLS LIMITED

  公开号：EP1526159B1

  公开（公告）日：2010-06-16
• JPH02282385A
  申请人：——

  公开号：JPH02282385A

  公开（公告）日：1990-11-19
• Organic dye, photoelectric conversion material, semiconductor electrode and photoelectric conversion device
  申请人：Horiuchi Tamotsu

  公开号：US20080149175A1

  公开（公告）日：2008-06-26

  Disclosed are an organic dye having a specific structure, a photoelectric conversion material containing the dye, a semiconductor electrode formed of a substrate having an electrically conductive surface, a semiconductor layer coated on the electrically conductive surface and the above dye adsorbed on the surface, and a photoelectric conversion device to which the above dye is applied. The present invention uses the above dye and can therefore provide a photoelectric conversion device excellent in photoelectric conversion efficiency, and the photoelectric conversion device is suitable for use in a solar cell or the like.
• ANTIVIRAL AGENTS, ANTIVIRAL FIBERS AND ANTIVIRAL FIBER STRUCTURES
  申请人：Matsushita Miki

  公开号：US20100221307A1

  公开（公告）日：2010-09-02

  Provided are antiviral agents that are effective in inactivating viruses, and fiber products and fiber structures carrying these antiviral agents. The antiviral agent effectives against influenza and comprises a metal phthalocyanine derivative represented by formula I. Fiber carries these antiviral agents.