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2,3-diphenyl-5,7-di(thiophen-2-yl)thieno[3,4-b]pyrazine | 868618-53-5

中文名称
——
中文别名
——
英文名称
2,3-diphenyl-5,7-di(thiophen-2-yl)thieno[3,4-b]pyrazine
英文别名
2,3-Diphenyl-5,7-bis(2-thienyl)thieno[3,4-b]pyrazine;2,3-diphenyl-5,7-dithiophen-2-ylthieno[3,4-b]pyrazine
2,3-diphenyl-5,7-di(thiophen-2-yl)thieno[3,4-b]pyrazine化学式
CAS
868618-53-5
化学式
C26H16N2S3
mdl
——
分子量
452.624
InChiKey
RBGZHZPBXBRUNU-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:
    616.6±50.0 °C(Predicted)
  • 密度:
    1.332±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    7
  • 重原子数:
    31
  • 可旋转键数:
    4
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    111
  • 氢给体数:
    0
  • 氢受体数:
    5

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2,3-diphenyl-5,7-di(thiophen-2-yl)thieno[3,4-b]pyrazineN-溴代丁二酰亚胺(NBS) 作用下, 以 四氢呋喃 为溶剂, 以50.4%的产率得到5,7-bis(5-bromothiophen-2-yl)-2,3-diphenylthieno[3,4-b]pyrazine
    参考文献:
    名称:
    Dual functions of a novel low-gap polymer for near infra-red photovoltaics and light-emitting diodes
    摘要:
    我们合成并表征了一种具有广泛吸收特性的新型低间隙共轭聚合物。在与 C70 衍生物的混合物中,我们展示了 0.76% 的功率转换效率。我们展示了聚合物的电致发光峰值为 956 nm,混合物中的量子效率为 0.02%。
    DOI:
    10.1039/c1cc12752g
  • 作为产物:
    描述:
    联苯甲酰2,5-二(2-噻吩基)-3,4-二胺甲醇 为溶剂, 反应 2.0h, 以120 mg的产率得到2,3-diphenyl-5,7-di(thiophen-2-yl)thieno[3,4-b]pyrazine
    参考文献:
    名称:
    Dual functions of a novel low-gap polymer for near infra-red photovoltaics and light-emitting diodes
    摘要:
    我们合成并表征了一种具有广泛吸收特性的新型低间隙共轭聚合物。在与 C70 衍生物的混合物中,我们展示了 0.76% 的功率转换效率。我们展示了聚合物的电致发光峰值为 956 nm,混合物中的量子效率为 0.02%。
    DOI:
    10.1039/c1cc12752g
点击查看最新优质反应信息

文献信息

  • METHOD OF THERMOCLEAVING A POLYMER LAYER
    申请人:Krebs Frederik Christian
    公开号:US20110045628A1
    公开(公告)日:2011-02-24
    A method of thermocleaving a thermocleavable polymer layer which is in thermal contact with a heat sensitive component that is not tolerant of the temperature required for thermocleavage of the thermocleavable polymer layer, in which the thermocleavable polymer layer is illuminated with a light source having a wavelength range more strongly absorbed by the thermocleavable polymer and substantially less strongly absorbed by the heat sensitive component, such that the thermocleavable polymer layer reaches a temperature sufficient to cause thermocleavage of the polymer without causing detrimental heating to the heat sensitive component. Further provided is apparatus for carrying out the above method.
    一种热解可分解聚合物层的方法,该层与热敏感元件保持热接触,但热敏感元件不能耐受热解所需的温度,其中,热解可分解聚合物层被照射具有更强吸收热解可分解聚合物的波长范围的光源,且该波长范围被热敏感元件吸收的强度显著较小,以使热解可分解聚合物层达到足够的温度,从而引起聚合物的热解,而不会对热敏感元件造成有害加热。此外还提供了用于执行上述方法的装置。
  • AIR STABLE PHOTOVOLTAIC DEVICE
    申请人:Krebs Frederik Christian
    公开号:US20110030789A1
    公开(公告)日:2011-02-10
    A method of forming a conducting polymer based photovoltaic device including: (a) providing a transparent first electrode; (b) providing the transparent first electrode with a layer of metal oxide nanoparticles, wherein the metal oxide is selected from the group consisting of: TiO 2 , TiO x , and ZnO; (c) providing the layer of metal oxide nanoparticles with a bulk hetero junction layer including metal oxide nanoparticles and a hole conducting polymer containing thermocleavable groups, wherein the metal oxide is selected from the group consisting of: TiO 2 , TiO x , CeO 2 , Nb 2 O 5 and ZnO; (d) heating the bulk heterojunction layer, to cleave the thermally cleavable groups to produce an insoluble hole containing polymer; (e) providing the bulk heterojunction layer with a hole transporting layer; and (f) providing the hole transporting layer with a second electrode. Also a conducting polymer based photovoltaic device, and polymeric compounds suitable for use in such devices and methods.
    一种形成基于导电聚合物的光伏器件的方法,包括:(a)提供透明的第一电极;(b)在透明的第一电极上提供一层金属氧化物纳米颗粒,其中所述金属氧化物被选自以下组:TiO2,TiOx和ZnO;(c)在金属氧化物纳米颗粒层上提供包括金属氧化物纳米颗粒和含有热可解组分的孔传导聚合物的大杂交层,其中所述金属氧化物被选自以下组:TiO2,TiOx,CeO2,Nb2O5和ZnO;(d)加热大杂交层,以裂解热可解组分,产生不溶的孔含聚合物;(e)在大杂交层上提供孔传输层;和(f)在孔传输层上提供第二电极。还提供了一种基于导电聚合物的光伏器件和适用于此类器件和方法的聚合物化合物。
  • Green electrochromic (EC) material and device
    申请人:Liu Lu
    公开号:US20070177243A1
    公开(公告)日:2007-08-02
    Three green EC materials based on thiophene, and a green EC material based on pyrazine are disclosed. A first thiophene derivative (2,3-Di-thiophen-2-yl-thieno[3,4-b]pyrazine), which was previously investigated as a nonlinear optical material, is here disclosed for its use as an EC material, and for its incorporation into an EC device. Synthesis of two new thiophene derivatives (2,5-di(thien-2-yl)-3,4-di(2,2,2-trifluoro-ethoxy)-thiophene and 2,5-(2,3-dihydro-thieno[3,4-b][1,4]dioxin-5-yl)-3,4-di(2,2,2-trifluoro-ethoxy)-thiophene), and a new pyrazine derivative (2,3-dibenzyl-5,7-di(thien-2-yl)thieno[3,4-b]pyrazine) are also disclosed, since these materials are all able to selectively change to a green color state, and can be polymerized to achieve a green EC polymer.
  • CARBON NANOTUBE COMPOSITE, ORGANIC SEMICONDUCTOR COMPOSITE, AND FIELD-EFFECT TRANSISTOR
    申请人:Jo Yukari
    公开号:US20110121273A1
    公开(公告)日:2011-05-26
    A carbon nanotube composite in which a conjugated polymer containing repeating units containing a fused heteroaryl unit having a nitrogen-containing double bond in the ring, and a thiophene unit is attached to at least a part of the surface of a carbon nanotube. The present invention reduces the hysteresis of a field-effect transistor having a semiconductor layer containing a carbon nanotube.
  • US7298541B2
    申请人:——
    公开号:US7298541B2
    公开(公告)日:2007-11-20
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同类化合物

试剂2,2'-Thieno[3,2-b]thiophene-2,5-diylbis-3-thiophenecarboxylicacid 苯并[b]噻吩,3-(2-噻嗯基)- 甲基[2,3'-联噻吩]-5-羧酸甲酯 牛蒡子醇 B 十四氟-Alpha-六噻吩 三丁基(5''-己基-[2,2':5',2''-三联噻吩]-5-基)锡 α-四联噻吩 α-六噻吩 α-五联噻吩 α-七噻吩 α,ω-二己基四噻吩 5,5′-双(3-己基-2-噻吩基)-2,2′-联噻吩 α,ω-二己基六联噻吩 Α-八噻吩 alpha-三联噻吩甲醇 alpha-三联噻吩 [3,3-Bi噻吩]-2,2-二羧醛 [2,2’]-双噻吩-5,5‘-二甲醛 [2,2':5',2''-三联噻吩]-5,5''-二基双[三甲基硅烷] [2,2'-联噻吩]-5-甲醇,5'-(1-丙炔-1-基)- [2,2'-联噻吩]-5-甲酸甲酯 [2,2'-联噻吩]-5-乙酸,a-羟基-5'-(1-炔丙基)-(9CI) C-[2,2-二硫代苯-5-基甲基]胺 5’-己基-2,2’-联噻吩-5-硼酸频哪醇酯 5-辛基-1,3-二(噻吩-2-基)-4H-噻吩并[3,4-c]吡咯-4,6(5H)-二酮 5-苯基-2,2'-联噻吩 5-溴5'-辛基-2,2'-联噻吩 5-溴-5′-己基-2,2′-联噻吩 5-溴-5'-甲酰基-2,2':5'2'-三噻吩 5-溴-3,3'-二己基-2,2'-联噻吩 5-溴-3'-癸基-2,2':5',2''-三联噻吩 5-溴-2,2-双噻吩 5-溴-2,2'-联噻吩-5'-甲醛 5-氯-5'-苯基-2,2'-联噻吩 5-氯-2,2'-联噻吩 5-正辛基-2,2'-并噻吩 5-己基-5'-乙烯基-2,2'-联噻吩 5-己基-2,2-二噻吩 5-全氟己基-5'-溴-2,2'-二噻吩 5-全氟己基-2,2′-联噻吩 5-乙酰基-2,2-噻吩基 5-乙氧基-2,2'-联噻吩 5-丙酰基-2,2-二噻吩 5-{[[2,2'-联噻吩]-5-基}噻吩-2-腈 5-[5-(5-己基噻吩-2-基)噻吩-2-基]噻吩-2-羧酸 5-(羟甲基)-[2,2]-联噻吩 5-(噻吩-2-基)噻吩-2-甲腈 5-(5-甲酰基-3-己基噻吩-2-基)-4-己基噻吩-2-甲醛 5-(5-甲基噻吩-2-基)噻吩-2-甲醛 5-(5-噻吩-2-基噻吩-2-基)噻吩-2-羧酸 5-(5-乙炔基噻吩-2-基)噻吩-2-甲醛