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1,6,7,12-四氯-3,4,9,10-四甲酸酰胺 | 115662-06-1

中文名称
1,6,7,12-四氯-3,4,9,10-四甲酸酰胺
中文别名
——
英文名称
N,N-dihydro-1,6,7,12-tetrachloro-3,4,9,10-tetracarboxyl perylene bisimide
英文别名
TCPDI;1,6,7,12-tetrachloroperylen-3,4:9,10-tetracarboxylic acid diimide;5,6,12,13-tetrachloroanthra(2,1,9-def:6,5,10-d'e'f')diisoquinoline-1,3,8,10(2H,9H)-tetrone;11,14,22,26-tetrachloro-7,18-diazaheptacyclo[14.6.2.22,5.03,12.04,9.013,23.020,24]hexacosa-1(22),2(26),3,5(25),9,11,13,15,20,23-decaene-6,8,17,19-tetrone
1,6,7,12-四氯-3,4,9,10-四甲酸酰胺化学式
CAS
115662-06-1
化学式
C24H6Cl4N2O4
mdl
——
分子量
528.135
InChiKey
SOGFVOVSOPPQPF-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    917.6±65.0 °C(Predicted)
  • 密度:
    1.885±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.9
  • 重原子数:
    34
  • 可旋转键数:
    0
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    92.3
  • 氢给体数:
    2
  • 氢受体数:
    4

安全信息

  • 危险品标志:
    Xn
  • 安全说明:
    S22,S36/37
  • 危险类别码:
    R62

反应信息

  • 作为反应物:
    描述:
    1,6,7,12-四氯-3,4,9,10-四甲酸酰胺 在 sodium dithionite 、 sodium hydroxide 作用下, 以 乙腈 为溶剂, 生成 2Na(1+)*TCPDI(2-)
    参考文献:
    名称:
    Self-assembly of twisted tetrachloroperylenediimide chromophores into two dimensional brick-stone aggregates: exciton dynamics and photoconductivity
    摘要:
    二维自组装已经在具有扭曲发色团的吡咯烷二酰亚胺中得到了证实,其中π-π堆积单元通过氢键相互作用相互连接。光谱测量和理论计算表明组装中存在微弱的J型激子耦合。二维晶体的高光导率使其成为进一步光电子应用的理想选择。
    DOI:
    10.1039/c2cc32112b
  • 作为产物:
    描述:
    1,6,7,12-四氯-3,4,9,10-苝四甲酸二酐 在 ammonium acetate 、 丙酸 作用下, 反应 8.0h, 以90%的产率得到1,6,7,12-四氯-3,4,9,10-四甲酸酰胺
    参考文献:
    名称:
    Self-assembly of twisted tetrachloroperylenediimide chromophores into two dimensional brick-stone aggregates: exciton dynamics and photoconductivity
    摘要:
    二维自组装已经在具有扭曲发色团的吡咯烷二酰亚胺中得到了证实,其中π-π堆积单元通过氢键相互作用相互连接。光谱测量和理论计算表明组装中存在微弱的J型激子耦合。二维晶体的高光导率使其成为进一步光电子应用的理想选择。
    DOI:
    10.1039/c2cc32112b
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文献信息

  • An Anionic Imide Material Having Ferromagnetism At Room Temperature And The Use Thereof
    申请人:South China University Of Technology
    公开号:US20200247802A1
    公开(公告)日:2020-08-06
    The anionic imide material is obtained by preparing a solution or a suspension of an imide compound, then reducing and drying the same; the anionic material comprises anions of an imide compound, the anions being at least one selected from the following formula I or formula II; in formula I or II: n=1, 2, or 3; R 1 , R 2 are respectively selected from at least one of H, amino, carboxyl, hydroxy, thiol, and pyridyl groups; X 1 -X 4 are respectively an electron withdrawing group, and specifically selected from one of H, F, Cl, Br, CN, and NO 2 groups. The anionic material of the present invention has a Curie temperature larger than room temperature and ferromagnetism, and is an organic magnetic material; it may be used for preparing an organic magnetic material and/or an organic magnetic device.
    阴离子酰亚胺材料是通过制备酰亚胺化合物的溶液或悬浮液,然后还原和干燥而得到的;该阴离子材料包括酰亚胺化合物的阴离子,该阴离子至少选择以下公式I或公式II中的一种;在公式I或II中:n = 1、2或3;R1、R2分别选择至少一个H、基、羧基、羟基、醇和吡啶基;X1-X4分别是电子提取基团,并特别选择自H、F、Cl、Br、CN和NO2基团中的一种。本发明的阴离子材料具有大于室温的居里温度和磁性,并且是一种有机磁性材料;它可用于制备有机磁性材料和/或有机磁性器件。
  • Anionic imide material having ferromagnetism at room temperature and the use thereof
    申请人:South China University Of Technology
    公开号:US11084816B2
    公开(公告)日:2021-08-10
    The anionic imide material is obtained by preparing a solution or a suspension of an imide compound, then reducing and drying the same; the anionic material comprises anions of an imide compound, the anions being at least one selected from the following formula I or formula II; in formula I or II: n=1, 2, or 3; R1, R2 are respectively selected from at least one of H, amino, carboxyl, hydroxy, thiol, and pyridyl groups; X1-X4 are respectively an electron withdrawing group, and specifically selected from one of H, F, Cl, Br, CN, and NO2 groups. The anionic material of the present invention has a Curie temperature larger than room temperature and ferromagnetism, and is an organic magnetic material; it may be used for preparing an organic magnetic material and/or an organic magnetic device.
    该阴离子酰亚胺材料是通过制备酰亚胺化合物的溶液或悬浮液,然后将其还原和干燥而得到的;该阴离子材料包括酰亚胺化合物的阴离子,该阴离子至少选自下式I或式II中的一种;在式I或式II中,n=1、2或3;R1、R2分别选自H、基、羧基、羟基、醇基和吡啶基中的至少一种;X1-X4分别是取电子基团,具体选自H、F、Cl、Br、CN和NO2基团中的一种。本发明的阴离子材料居里温度大于室温,具有磁性,是一种有机磁性材料,可用于制备有机磁性材料和/或有机磁性器件。
  • FLUORIERTE RYLENTETRACARBONSÄUREDERIVATE UND DEREN VERWENDUNG
    申请人:BASF SE
    公开号:EP1987092B1
    公开(公告)日:2013-05-22
  • METHOD FOR PRODUCING ORGANIC FIELD-EFFECT TRANSISTORS
    申请人:Konemann Martin
    公开号:US20070259475A1
    公开(公告)日:2007-11-08
    A method for producing an organic field-effect transistor, comprising the steps of: a) providing a substrate comprising a gate structure, a source electrode and a drain electrode located on the substrate, and b) applying an n-type organic semiconducting compound to the area of the substrate where the gate structure, the source electrode and the drain electrode are located, wherein the n-type organic semiconducting compound is selected from the group consisting of compounds of the formula I wherein R 1 , R 2 , R 3 and R 4 are independently hydrogen, chlorine or bromine, with the proviso that at least one of these radicals is not hydrogen, Y 1 is O or NR a , wherein R a is hydrogen or an organyl residue, Y 2 is O or NR b , wherein R b is hydrogen or an organyl residue, Z 1 , Z 2 , Z 3 and Z 4 are O, where, in the case that Y 1 is NR a , one of the residues Z 1 and Z 2 may be a NR c group, where R a and R c together are a bridging group having 2 to 5 atoms between the terminal bonds, where, in the case that Y 2 is NR b , one of the residues Z 3 and Z 4 may be a NR d group, where R b and R d together are a bridging group having 2 to 5 atoms between the terminal bonds.
  • VERFAHREN ZUR HERSTELLUNG VON MIT RYLENTETRACARBONSAEUREDIIMIDEN BESCHICHTETEN SUBSTRATEN
    申请人:Konemann Martin
    公开号:US20090078312A1
    公开(公告)日:2009-03-26
    The present invention relates to a process for producing a substrate coated with rylenetetracarboximides, in which a substrate is treated with an N,N′-bisubstituted rylenetetracarboximide and the treated substrate is heated to a temperature at which the N,N′-bisubstituted rylenetetracarboximide is converted to the corresponding N,N′-unsubstituted compound. The present invention further relates to semiconductor units, organic solar cells, excitonic solar cells and organic light-emitting diodes which comprise a substrate produced by this process. The present invention further relates to a process for preparing N,N′-unsubstituted rylenetetracarboximides, in which the corresponding N,N′-bisubstituted rylenetetracarboximides are provided and heated to a temperature at which these compounds are converted to the corresponding N,N′-unsubstituted compounds.
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