1-氯-9,10-二苯基蒽 | 43217-27-2

• 分子结构分类: 有机化合物 - 木脂素、新木脂素和相关化合物 - 芳基萘木脂素
• 中文名称: 1-氯-9,10-二苯基蒽
• 英文名称: 1-chloro-9,10-diphenylanthracene
• 英文别名: 1-chloro-9,10-diphenyl-anthracene；1-Chlor-9,10-diphenyl-anthracen；1-Chlor-9,10-diphenylanthracen
• CAS: 43217-27-2
• 化学式: C₂₆H₁₇Cl
• 分子量: 364.874
• InChiKey: VVCSLEYASKOQEN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  8.3
• 重原子数：
  27
• 可旋转键数：
  2
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

安全信息

• 海关编码：
  2903999090

反应信息

• 作为反应物：
  描述：

  1-氯-9,10-二苯基蒽 在 二硫化碳 作用下， 生成 1-chloro-9,10-diphenyl-9,10-dihydro-9,10-epidioxido-anthracene
  参考文献：
  名称：

  Mellier, Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1944, vol. 219, p. 188

  摘要：

  DOI：
• 作为产物：
  描述：

  1-氯蒽醌 在 溶剂黄146 、 potassium iodide 作用下， 生成 1-氯-9,10-二苯基蒽
  参考文献：
  名称：

  Mellier, Annales de Chimie (Cachan, France), 1955, vol. <12> 10, p. 666,682

  摘要：

  DOI：

文献信息

• Fabrication of cellular NiTi intermetallic compounds
  作者：Bing-Yun Li、Li-Jian Rong、Yi-Yi Li、V. E. Gjunter

  DOI：10.1557/jmr.2000.0004

  日期：2000.1

  Self-propagating high-temperature synthesis (SHS) has been successfully developed for the fabrication of cellular NiTi intermetallic compounds, which have an open cellular structure with about 60 vol% porosity and more than 95% open-porosity ratio. The SHS reactions lead to the formation of TiNi, Ti₂Ni, Ni₃Ti, and Ni₄Ti₃ intermetallics. The SHS process can be controlled by regulating the preheating temperature, which has effects on the phase amount and the shape as well as macrodistribution of pores in the products.

  自蔓延高温合成（SHS）已成功用于制造蜂窝状镍钛金属间化合物，这种金属间化合物具有开放的蜂窝状结构，孔隙率约为 60%，开放孔隙率超过 95%。SHS 反应可形成 TiNi、Ti2Ni、Ni3Ti 和 Ni4Ti3 金属间化合物。SHS 过程可通过调节预热温度来控制，预热温度对产品中的相量、孔隙形状和宏观分布都有影响。
• An electroluminescent element
  申请人：ASAHI KASEI KOGYO KABUSHIKI KAISHA

  公开号：EP0532798A1

  公开（公告）日：1993-03-24

  Disclosed is an electroluminescent element comprising an anode, a cathode and, disposed therebetween, an organic luminescent layer comprising a mixture of a fluorescent luminescent agent, at least one hole moving and donating agent capable of moving holes and donating the same to the luminescent agent and at least one electron moving and donating agent capable of moving electrons and donating the same to the luminescent agent. In the element, the components of the luminescent layer have specific oxidation potential and reduction potential relationships. The element emits light in response to electrical signals. The element exhibits high luminescence efficiency and brightness even at low voltages, and it can efficiently be produced at low cost.

  本发明公开了一种电致发光元件，该元件包括阳极、阴极和置于其间的有机发光层，有机发光层包括荧光发光剂、至少一种能够移动空穴并将空穴捐献给发光剂的空穴移动和捐献剂以及至少一种能够移动电子并将电子捐献给发光剂的电子移动和捐献剂的混合物。在元件中，发光层的各组分具有特定的氧化电位和还原电位关系。该元件在电信号的作用下发光。这种元件即使在低电压下也能表现出很高的发光效率和亮度，而且能以低成本高效生产。
• Photopolymerization sensitizer composition
  申请人：Kawasaki Kasei Chemicals Ltd.

  公开号：US11352450B2

  公开（公告）日：2022-06-07

  The purpose of the present invention is to provide a photopolymerizable composition which can act as a photopolymerization sensitizer that is active against light having a wavelength falling within a wavelength range of from 300 to 500 nm, and which has such a property that coloring of a cured product produced by polymerizing a photopolymerizable composition containing the photopolymerization sensitizer is less. A photopolymerization sensitizer composition characterized by comprising a photopolymerization sensitizer containing an alkoxyanthracene compound represented by the formula (1) and a singlet oxygen quencher; and a photopolymerizable composition containing the photopolymerization sensitizer composition: in the formula (1), n represents an integer of 1 or 2; R represents a C1-12 alkyl group; and X represents a hydrogen atom or a C1-8 alkyl group.

  本发明的目的是提供一种可光聚合组合物，该组合物可作为光聚合敏化剂，对波长在300至500纳米范围内的光具有活性，并且具有这样一种特性，即通过聚合含有该光聚合敏化剂的可光聚合组合物而生产的固化产品着色较少。 一种光聚合增感剂组合物，其特征在于包括含有式（1）表示的烷氧蒽化合物和单线态氧淬灭剂的光聚合增感剂；以及含有该光聚合增感剂组合物的可光聚合组合物： 式（1）中，n 代表 1 或 2 的整数；R 代表 C1-12 烷基；X 代表氢原子或 C1-8 烷基。
• 189. 2 : 3-Benzorubicene, rubicene, and their derivatives
  作者：E. Clar、W. Willicks

  DOI：10.1039/jr9580000942

  日期：——
• Synthesis of Triphenylene
  作者：Ernst Bergmann、O. Blum-Bergmann

  DOI：10.1021/ja01287a010

  日期：1937.8

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