6-(3,6,7,10,11-Pentapentoxytriphenylen-2-yl)oxyhexyl acetate | 111689-39-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 菲及其衍生物
• 英文名称: 6-(3,6,7,10,11-Pentapentoxytriphenylen-2-yl)oxyhexyl acetate
• CAS: 111689-39-5
• 化学式: C₅₁H₇₆O₈
• 分子量: 817.16
• InChiKey: PMLKMWCCMHFQQE-UHFFFAOYSA-N

物化性质

• 沸点：
  847.4±65.0 °C(Predicted)
• 密度：
  1.040±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  15
• 重原子数：
  59
• 可旋转键数：
  34
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.63
• 拓扑面积：
  81.7
• 氢给体数：
  0
• 氢受体数：
  8

反应信息

• 作为反应物：
  描述：

  6-(3,6,7,10,11-Pentapentoxytriphenylen-2-yl)oxyhexyl acetate 、 偶氮苯-4,4’-二羧酸二乙酯 在 titanium(IV) isopropylate 作用下， 生成 bis(6-((3,6,7,10,11-pentakis(pentyloxy)triphenylen-2-yl)oxy)hexyl) 4,4'-(diazene-1,2-diyl)(E)-dibenzoate 、 bis(6-((3,6,7,10,11-pentakis(pentyloxy)triphenylen-2-yl)oxy)hexyl) 4,4'-(diazene-1,2-diyl)(E)-dibenzoate
  参考文献：
  名称：

  Kreuder, Willi; Ringsdorf, Helmut; Herrmann-Schoenherr, Otto, Angewandte Chemie, 1987, vol. 99, # 12, p. 1300 - 1303

  摘要：

  DOI：
• 作为产物：
  描述：

  6-氯-1-己醇 、 2-acetyloxy-3,6,7,10,11-pentakis(pentyloxy)triphenylene 在 potassium carbonate 、 乙酸乙酯 、 potassium iodide 、 silver(l) oxide 作用下， 生成 6-(3,6,7,10,11-Pentapentoxytriphenylen-2-yl)oxyhexan-1-ol 、 6-(3,6,7,10,11-Pentapentoxytriphenylen-2-yl)oxyhexyl acetate
  参考文献：
  名称：

  Kreuder, Willi; Ringsdorf, Helmut; Herrmann-Schoenherr, Otto, Angewandte Chemie, 1987, vol. 99, # 12, p. 1300 - 1303

  摘要：

  DOI：

文献信息

• Use of Methanofullerne Derivatives as Resist Materials and Method for Forming a Resist Layer
  申请人：Robinson Alex

  公开号：US20080118874A1

  公开（公告）日：2008-05-22

  The use as a resist material of a methanofullerene derivative having a plurality of open-ended addends, and to a method for forming a patterned resist layer on a substrate using the methanofullerene derivatives. The methanofullerene derivatives can be represented by the formal C 2x (CR 1 R 2 ) m where x is at least 10, m is at least 2, each addend represented by CR 1 R 2 is the same or different, and wherein each R 1 and R 2 is each a monovalent organic group, or a divalent organic group which forms a ring structure by being joined to the fullerene shell, or where both R 1 and R 2 of an addend are divalent groups, they may be mutually joined to form a ring structure, save that at least two of R 1 or two of R 2 are monovalent, or a mixture of such derivatives. The use of any methanofullerene derivative which has been chemically amplified for formation of a patterned resist layer. The essential step of the method is forming a coating layer comprising the methanofullerene derivative on the substrate surface, the methanofullerene derivative being chemically amplified by including in the coating layer at least one additional component which increases the sensitivity of the exposed layer to actinic radiation which is subsequently used to pattern the layer.