摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

5,10-dioxo-5,10-dihydro-benzo[1,2-b;4,5-b']bis[1,4]dithiine-2,3,7,8-tetracarbonitrile | 23078-32-2

中文名称
——
中文别名
——
英文名称
5,10-dioxo-5,10-dihydro-benzo[1,2-b;4,5-b']bis[1,4]dithiine-2,3,7,8-tetracarbonitrile
英文别名
5,10-Dioxo-[1,4]dithiino[2,3-g][1,4]benzodithiine-2,3,7,8-tetracarbonitrile
5,10-dioxo-5,10-dihydro-benzo[1,2-<i>b</i>;4,5-<i>b</i>']bis[1,4]dithiine-2,3,7,8-tetracarbonitrile化学式
CAS
23078-32-2
化学式
C14N4O2S4
mdl
——
分子量
384.444
InChiKey
FTOYXCYNGNXXQP-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

计算性质

  • 辛醇/水分配系数(LogP):
    2.2
  • 重原子数:
    24
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    231
  • 氢给体数:
    0
  • 氢受体数:
    10

反应信息

点击查看最新优质反应信息

文献信息

  • PHOSPHINE OXIDE COMPOUND, ORGANIC ELECTROLUMINESCENCE ELEMENT, PRODUCTION METHOD AND USES THEREOF
    申请人:TERASHIMA Takashi
    公开号:US20120256536A1
    公开(公告)日:2012-10-11
    A compound having a stable deposition rate suitable for forming an electron-transporting layer of an organic El element. The compound is represented by the following formula (1): wherein in the formula (1), plural R 1 are each an alkyl group having 1 to 10 carbon atoms, an alkoxy group having 1 to 10 carbon atoms, a halogen atom, or a hydrogen atom, and may be the same as or different from one another; and plural Ar are each a monovalent substituted or unsubstituted aromatic group optionally containing a hetero atom, and may be the same as or different from one another.
    一种化合物,具有稳定的沉积速率,适用于形成有机EL元件的电子传输层。该化合物由以下公式(1)表示:其中,在公式(1)中,复数R1分别是具有1到10个碳原子的烷基基团,具有1到10个碳原子的烷氧基团,卤素原子或氢原子,并且可以相同或不同; 复数Ar分别是具有杂原子的单价取代或未取代芳香基团,可以相同或不同。
  • Novel quinone-type acceptors fused with sulphur heterocycles and their highly conductive complexes with electron donors
    作者:Yoshiro Yamashita、Takanori Suzuki、Gunzi Saito、Toshio Mukai
    DOI:10.1039/c39860001489
    日期:——
    p-Benzoquinone derivatives fused with sulphur-containing heterocycles are strong electron acceptors and some of their charge transfer complexes with electron donors show high electrical conductivities.
    与含硫杂环稠合的对苯醌衍生物是强电子受体,它们与电子给体的某些电荷转移络合物显示出高电导率。
  • Aromatic Amine-Terphenyl Compounds and Use Thereof in Organic Semiconducting Components
    申请人:Novaled GmbH
    公开号:US20150011795A1
    公开(公告)日:2015-01-08
    The present invention relates to aromatic amine-terphenyl compounds and use thereof in organic semiconducting components.
    本发明涉及芳香胺-三苯基化合物及其在有机半导体元件中的应用。
  • Charge Transporting Semi-Conducting Material and Semi-Conducting Device
    申请人:NOVALED GMBH
    公开号:US20150349262A1
    公开(公告)日:2015-12-03
    The present invention relates to a charge transporting semi-conducting material comprising: a) optionally at least one electrical dopant, and b) at least one cross-linked charge-transporting polymer comprising 1,2,3-triazole cross-linking units, a method for its preparation and a semiconducting device comprising the charge transporting semi-conducting material.
    本发明涉及一种电荷传输半导体材料,包括:a) 可选的至少一种电性掺杂剂;和b) 至少一种交联的电荷传输聚合物,其中包括1,2,3-三唑交联单元,以及其制备方法和包括该电荷传输半导体材料的半导体器件。
  • METHOD OF DOPING ORGANIC SEMICONDUCTORS WITH QUINONEDIIMINE DERIVATIVES
    申请人:Kuehl Olaf
    公开号:US20050121667A1
    公开(公告)日:2005-06-09
    The invention relates to the use of an organic mesomeric compound as organic dopant for doping an organic semiconducting matrix material for varying the electrical properties thereof. In order to be able to handle organic semiconductors more easily in the production process and to be able to produce electronic components with doped organic semiconductors more reproducibly, a quinone or quinone derivative or a 1,3,2-dioxaborine or a 1,3,2-dioxaborine derivative may be used as a mesomeric compound, which under like evaporation conditions has a lower volatility than tetrafluorotetracyanoquinonedimethane (F4TCNQ).
    本发明涉及使用有机共振化合物作为有机掺杂剂,以掺杂有机半导体基质材料,从而改变其电学性质。为了能够更容易地在生产过程中处理有机半导体材料,并能够更可靠地生产掺杂有机半导体的电子元件,可以使用醌或醌衍生物或1,3,2-二氧硼杂环或1,3,2-二氧硼杂环衍生物作为共振化合物,其在相同的蒸发条件下具有比四氟四氰基苯醌二甲烷(F4TCNQ)更低的挥发性。
查看更多

同类化合物

硅烷,1,9-硫杂蒽二基二[三甲基- 甲硫芬 噻蒽-2-硼酸 噻蒽-1,9-二甲酸 噻蒽 5-氧化物 噻蒽 5,10-二氧化物 噻蒽 噻吩-1-羧酸 噻吩-1-硼酸 六氟磷酸1-氯-5-苯基-硫杂蒽-5-正离子 二甲基噻蒽 2-溴噻蒽 2-吗啉-4-基-6-噻蒽-1-基吡喃-4-酮 2,7-噻蒽二甲酸 2,7-二氟噻蒽 2,7-二乙酰基噻蒽 2,3,7,8-四甲基-1,4,6,9-噻蒽四酮 2,3,7,8-四氯噻蒽 1,4,6,9-噻蒽四酮 2,7-bis(9-carbazolyl)thianthrene 1,7-dimethylthianthrene 13,13,14,14-Tetracyano-2-methylbenzonaphtho<2,3-e><1,4>dithiin-6,11-quinodimethane 2-methyl-5,12-dithianaphthacene 13,13,14,14-Tetracyanobenzonaphtho<2,3-e><1,4>dithiin-6,11-quinodimethane 2,5-dihexylbenzo[5,6][1,4]dithiino[2,3-e]pyrrolo[3,4-g]isoindole-1,3,4,6(2H,5H)-tetraone 2-cyanothianthrene 1-cyanothianthrene 2,3-difluorothianthrene 3-(1-thianthrenyl)phenol 2,7-diisopropylthianthrene-5,5,10,10-tetraoxide (Z)-2-(5-thianthreniumyl)-2-hexene perchlorate (E)-2-(5-thianthreniumyl)-2-hexene perchlorate (Z)-3-(5-thianthreniumyl)-2-hexene perchlorate (E)-3-(5-thianthreniumyl)-2-hexene perchlorate Phenylthianthren-2-ylmethanol 1,1′-methylenedithianthrene 1,1′-(chloromethylene)dithianthrene 1,6-dithianthren-1-ylhexane-1,6-diol 9-(4-methylacetophenone)thianthrenium perchlorate Thianthren-1-ylphenylmethanol Diphenylthianthren-1-ylmethanol 4,4,5,5-tetramethyl-2-(thianthren-2-yl)-1,3,2-dioxaborolane thianthrene-2-sulfonic acid 2-(thianthren-1-ylsulfanyl)pyridine 2,8-dibromothianthrene dithianthren-1-ylmethanol 5-(2-acetamido-4,5-dimethylphenyl)thianthreniumyl perchlorate 5-(4-anisyl)thianthreniumyl perchlorate 1-tributylstannylthianthrene 5-(3-bromo-4-methoxyphenyl)thianthreniumyl perchlorate