9-bromoperylene-3,4-dicarboxylic anhydride | 676363-06-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 萘并吡喃类
• 英文名称: 9-bromoperylene-3,4-dicarboxylic anhydride
• 英文别名: 9-bromoperylene-3,4-dicarboxylic acid anhydride；9-bromo-3,4-perylenedicarboxylic anhydride；9-bromoperylene-3,4-dicarboxylic monoanhydride；5-bromo-16-oxahexacyclo[12.6.2.12,6.011,21.018,22.010,23]tricosa-1(20),2,4,6,8,10(23),11(21),12,14(22),18-decaene-15,17-dione
• CAS: 676363-06-7
• 化学式: C₂₂H₉BrO₃
• 分子量: 401.216
• InChiKey: BZPYSYIROOVUFG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.8
• 重原子数：
  26
• 可旋转键数：
  0
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  43.4
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  9-bromoperylene-3,4-dicarboxylic anhydride 在 四丁基溴化铵 、 palladium diacetate 、 三乙胺 作用下， 以 甲苯 为溶剂， 反应 12.0h， 以34%的产率得到5-(15,17-Dioxo-16-oxahexacyclo[12.6.2.12,6.011,21.018,22.010,23]tricosa-1(20),2,4,6,8,10(23),11(21),12,14(22),18-decaen-5-yl)-16-oxahexacyclo[12.6.2.12,6.011,21.018,22.010,23]tricosa-1(20),2,4,6,8,10(23),11(21),12,14(22),18-decaene-15,17-dione
  参考文献：
  名称：

  Controlling UV/vis Absorption and Stokes Shifts in Highly Fluorescent Chromophores by Molecular Dynamics in Targeted Construction of Dyads

  摘要：

  Perylenedicarboximides were interlinked in their free pen-position to form dyads where the UV/vis absorptivity was amplified by exciton effects and the strong fluorescence bathochromically shifted by molecular dynamics. Applications of this type of dye with such increased Stokes shifts were discussed.

  DOI：

  10.1021/jo301417p
• 作为产物：
  描述：

  2-(1-hexylheptyl)-1H-perylo[3,4-cd]pyridine-1,3(2H)-dione 在 硫酸 、 溴 、 碘 、 potassium hydroxide 作用下， 以 叔丁醇 为溶剂， 生成 9-bromoperylene-3,4-dicarboxylic anhydride
  参考文献：
  名称：

  Controlling UV/vis Absorption and Stokes Shifts in Highly Fluorescent Chromophores by Molecular Dynamics in Targeted Construction of Dyads

  摘要：

  Perylenedicarboximides were interlinked in their free pen-position to form dyads where the UV/vis absorptivity was amplified by exciton effects and the strong fluorescence bathochromically shifted by molecular dynamics. Applications of this type of dye with such increased Stokes shifts were discussed.

  DOI：

  10.1021/jo301417p

文献信息

• [EN] TERRYLENE COMPOUNDS, PREPARATION THEREOF AND USE THEREOF IN ORGANIC SOLAR CELLS<br/>[FR] COMPOSÉS TERRYLÈNES, LEUR PRÉPARATION ET LEUR UTILISATION DANS DES CELLULES SOLAIRES ORGANIQUES
  申请人：BASF SE

  公开号：WO2012123888A1

  公开（公告）日：2012-09-20

  A terrylene compound of the formula I and processes for preparation thereof are disclosed, (I) in which R1, R2, R3 and R4 are each independently selected from hydrogen and in each case unsubstituted or substituted alkyl, aryl, thiophenyl and oligothiophenyl; or in each case at least two adjacent radicals selected from the R1, R2, R3 and R4 radicals, together with the carbon atoms of the benzene ring to which they are bonded, may also be a fused ring system having 1, 2, 3, 4, 5, 6, 7 or 8 further rings, and A with the carbon atoms to which it is bonded is a fused monocyclic, dicyclic, tricyclic, tetracyclic, pentacyclic or hexacyclic ring system which optionally bears one or more independently selected substituents. Further disclosed is an organic solar cell with a photoactive region which comprises at least one organic donor material in contact with at least one organic acceptor material, wherein the photoactive region comprises at least one such terrylene compound.

  本公开了一种化学式I的苝基化合物及其制备方法，其中R1、R2、R3和R4分别独立地选自氢和未取代或取代的烷基、芳基、噻吩基和寡硫代噻吩基；或者在R1、R2、R3和R4基团中至少有两个相邻基团，连同它们结合的苯环的碳原子，也可以是具有1、2、3、4、5、6、7或8个进一步环的融合环系统；以及与其结合的碳原子的A是一个融合的单环、双环、三环、四环、五环或六环环系统，可选地带有一个或多个独立选择的取代基。此外，还公开了一种有机太阳能电池，其具有至少一个有机给体材料与至少一个有机受体材料接触的光活性区域，其中光活性区域至少包含一个这样的苝基化合物。
• DIBENZORYLENETETRACARBOXIMIDES AS INFRARED ABSORBERS
  申请人：Koenemann Martin

  公开号：US20100048904A1

  公开（公告）日：2010-02-25

  Dibenzorylenetetracarboximides of the general formula I in which the variables are each defined as follows: R′ are identical or different radicals: hydrogen; optionally substituted aryloxy, arylthio, hetaryloxy or hetarylthio; R are identical or different radicals: hydrogen; optionally substituted C 1 -C 30 -alkyl, C 3 -C 8 -cycloalkyl, aryl or hetaryl; m, n are each independently 0 or 1.

  一般式I的二苯并咔唑四羧酰亚胺中，变量定义如下：R′为相同或不同的基团：氢；可选择取代的芳氧基、芳硫基、杂芳氧基或杂芳硫基；R为相同或不同的基团：氢；可选择取代的C1-C30烷基、C3-C8环烷基、芳基或杂芳基；m，n各自独立地为0或1。
• LIQUID CRYSTALLINE RYLENE TETRACARBOXYLIC ACID DERIVATIVES AND USE THEREOF
  申请人：Koenemann Martin

  公开号：US20110042651A1

  公开（公告）日：2011-02-24

  The present invention relates to liquid-crystalline rylenetetracarboxylic acid derivatives, to processes for their preparation and to their use as n-type organic semiconductors for producing organic field-effect transistors and solar cells.

  本发明涉及液晶芳纶四羧酸衍生物，其制备方法以及作为n型有机半导体用于制造有机场效应晶体管和太阳能电池的用途。
• Synthesis and Optical Properties of Water-Soluble Polyglycerol-Dendronized Rylene Bisimide Dyes
  作者：Timm Heek、Frank Würthner、Rainer Haag

  DOI：10.1002/chem.201300556

  日期：2013.8.12

  new water‐soluble polyglycerol‐dendronized perylene, terrylene, and quaterrylene bisimides have been synthesized and characterized with respect to their optical properties in polar organic solvents and water by using UV/Vis and fluorescence spectroscopy. All of these dyes were highly soluble in water, but the size of the chosen polyglycerol dendron was only sufficient to completely suppress dye aggregation

  通过使用UV / Vis和荧光光谱法，已经合成了四种新的水溶性聚甘油-二烯化per，三萘嵌苯和四萘嵌苯双酰亚胺，并对其在极性有机溶剂和水中的光学性质进行了表征。所有这些染料都高度溶于水，但是所选聚甘油树枝状分子的大小仅足以完全抑制未取代核的per衍生物的染料聚集。它们在水中的高溶解度以及直至NIR区域的吸收和发射波长，使得未取代核的core和三萘嵌苯双酰亚胺是生物成像应用的理想候选物，而在所有极性溶剂中四萘嵌苯双酰亚胺均没有荧光，因此不值得进一步研究。该生色团在荧光和成像中的应用。
• GREEN ZINC PORPHYRIN SENSITIZERS AND THEIR APPLICATIONS
  申请人：YEH Chen-Yu

  公开号：US20130090469A1

  公开（公告）日：2013-04-11

  The present invention relates to zinc porphyrin-based photosensitive dyes, specifically to zinc porphyrin-based photosensitive dyes with green transparency. The photosensitive dyes exhibit high push-pull ability in the zinc porphyrin-based structure, higher absorption and power conversion efficiency. The photosensitive dyes are used in the manufacture of dye-sensitive solar cells.

  本发明涉及基于锌卟啉的光敏染料，具体地说是具有绿色透明度的基于锌卟啉的光敏染料。这些光敏染料在锌卟啉结构中表现出很高的推拉能力，具有更高的吸收和功率转换效率。这些光敏染料用于制造染料敏感太阳能电池。