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bis(ethylenedithio)-2,5-bis(1,3-dithio-2-ylidene)-2,5-dihydro-selenophene | 170800-02-9

中文名称
——
中文别名
——
英文名称
bis(ethylenedithio)-2,5-bis(1,3-dithio-2-ylidene)-2,5-dihydro-selenophene
英文别名
2-[5-(5,6-Dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidene)selenophen-2-ylidene]-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiine;2-[5-(5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidene)selenophen-2-ylidene]-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiine
bis(ethylenedithio)-2,5-bis(1,3-dithio-2-ylidene)-2,5-dihydro-selenophene化学式
CAS
170800-02-9
化学式
C14H10S8Se
mdl
——
分子量
513.721
InChiKey
IDTXGHHLMBCVQG-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):
    5.05
  • 重原子数:
    23
  • 可旋转键数:
    0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    202
  • 氢给体数:
    0
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Synthesis and X-ray crystal structure of a selenophenoquinonoid-extended donor, BEDT–BDTS, affording highly conducting tetracyanoquinodimethaneand I3 complexes
    摘要:
    2,5-双(4,5-乙撑二硫-1,3-二硫醇-2-亚基)-2,5-二氢硒酚++(BEDT-BDTS)是双(乙撑二硫)四硫富瓦烯(BEDT-TTF)的硒酚醌类扩展类似物,已合成为高Tc有机超导体电子供体组分的有前景候选物。BEDT-BDTS具有空气稳定性,与BEDT-TTF相比,其电子供体能力显著增强。BEDT-BDTS的分子和晶体结构已通过单晶X射线分析确定,其中在供体排列的并排方向上发现了短分子间SS接触。已获得1:1 TCNQ复合物和3:1 I3- BEDT-BDTS自由基阳离子盐,并证明其具有相当高的室温电导率。
    DOI:
    10.1039/a703428h
  • 作为产物:
    参考文献:
    名称:
    Synthesis and X-ray crystal structure of a selenophenoquinonoid-extended donor, BEDT–BDTS, affording highly conducting tetracyanoquinodimethaneand I3 complexes
    摘要:
    2,5-双(4,5-乙撑二硫-1,3-二硫醇-2-亚基)-2,5-二氢硒酚++(BEDT-BDTS)是双(乙撑二硫)四硫富瓦烯(BEDT-TTF)的硒酚醌类扩展类似物,已合成为高Tc有机超导体电子供体组分的有前景候选物。BEDT-BDTS具有空气稳定性,与BEDT-TTF相比,其电子供体能力显著增强。BEDT-BDTS的分子和晶体结构已通过单晶X射线分析确定,其中在供体排列的并排方向上发现了短分子间SS接触。已获得1:1 TCNQ复合物和3:1 I3- BEDT-BDTS自由基阳离子盐,并证明其具有相当高的室温电导率。
    DOI:
    10.1039/a703428h
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文献信息

  • Selenienoquinonoid-Extended Analogues of TTF, EDT-TTF, and BEDT-TTF. New Donors and Their Conductive Complexes
    作者:Kazuko Takahashi、Kensuke Tomitani、Toshihiro Ise、Takashi Shirahata
    DOI:10.1246/cl.1995.619
    日期:1995.8
    2,5-Bis(1,3-dithiol-2-ylidene)-2,5-dihydroselenophene (BDTS) and its ethylenedithio (EDT-BDTS) and bis(ethylenedithio) (BEDT-BDTS) derivatives, novel extended donors with a central selenium atom, have been synthesized by convenient methods. Of these, EDT-BDTS and BEDT-BDTS having outer chalcogen atoms afforded highly conducting molecular complexes with TCNQ (σ = 13 Scm−1 on a compressed pellet).
    我们采用简便的方法合成了 2,5-双(1,3-二硫醇-2-亚基)-2,5-二氢硒吩(BDTS)及其二硫代乙烷(EDT-BDTS)和二(二硫代乙烷)(BEDT-BDTS)衍生物,它们是具有一个中心硒原子的新型扩展供体。其中,EDT-BDTS 和 BEDT-BDTS 具有外层的查尔根原子,能与 TCNQ 形成高导电性的分子络合物(压缩颗粒上的σ = 13 Scm-1)。
  • Synthesis and X-ray crystal structure of a selenophenoquinonoid-extended donor, BEDT–BDTS, affording highly conducting tetracyanoquinodimethaneand I3 complexes
    作者:Kazuko Takahashi、Takashi Shirahata、Kensuke Tomitani
    DOI:10.1039/a703428h
    日期:——
    2,5-Bis(4,5-ethylenedithio-1,3-dithiol-2-ylidene)-2,5-dihydroselenophe++ne (BEDT–BDTS), a selenophenoquinonoid-extended analogue of bis(ethylenedithio)tetrathiafulvalenes (BEDT–TTF), has been synthesized as a promising candidate for an electron-donating component of highTc organic superconductors. BEDT–BDTS is air-stable and has a significantly enhanced electron-donating ability compared with that of BEDT–TTF. The molecular and crystal structures of BEDT–BDTS have been determined by single crystal X-ray analysis in which short intermolecular SS contacts have been found in the side-by-side directions of the donor arrangements. A 1:1 TCNQ complex and a 3:1 I3– radical cation salt of BEDT–BDTS have been obtained and proved to exhibit fairly high room temperature conductivities.
    2,5-双(4,5-乙撑二硫-1,3-二硫醇-2-亚基)-2,5-二氢硒酚++(BEDT-BDTS)是双(乙撑二硫)四硫富瓦烯(BEDT-TTF)的硒酚醌类扩展类似物,已合成为高Tc有机超导体电子供体组分的有前景候选物。BEDT-BDTS具有空气稳定性,与BEDT-TTF相比,其电子供体能力显著增强。BEDT-BDTS的分子和晶体结构已通过单晶X射线分析确定,其中在供体排列的并排方向上发现了短分子间SS接触。已获得1:1 TCNQ复合物和3:1 I3- BEDT-BDTS自由基阳离子盐,并证明其具有相当高的室温电导率。
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同类化合物

硒酚 硒吩并[3,2-B]噻吩 硒吩-3-羧酸 硒吩-2-羧酸 硒吩-2-硼酸 5-甲基-2-硒吩羰基氯化物 5-甲基-2-硒吩亚磺酸 3-硒吩羰基氯化物 3-甲基硒吩 3,4-双(氯甲基)-2,5-二甲基硒吩 2-甲基-硒吩 2-乙烯基硒吩 2,5-二-(2'-噻吩基)硒吩 2,2'-双硒 2,6-di(selenophen-2-yl)tetrahydro-4H-selenopyran-4-one 2-(2-(selenophen-2-yl)ethynyl)selenophene (2-selenophene-2-yl)lithium 2-(dec-1-ynyl)selenophene (3-selenienyl)di(1-adamantyl)methanol 5-Methyl-2-mercapto-selenophen seleno[3,4-b]thiophene 3-Selenophenethiol, 2,5-dimethyl- 2-dicyanomethylselenophene bis(3-selenienyl)methanol 2-Propyl-selenophen 2-(5'-hydroxymethyl-2'-selenyl)-thiophene 4,4,6,6-tetramethyl-2-{[(methylsulfonyl)thio]methyl}-4,6-dihydro-5H-selenolo[2,3-c]pyrrol-5-yloxyl radical selenosulflower 5-Carboxyseleno<2,3-b>thiophen methyl 4-[(dimethylamino)diazenyl]-5-methylselenophene-2-carboxylate ethyl selenopheno[3,2-b]thiophene-5-carboxylate 3-Cyanoselenophen 2,4-Ditert-butylselenophene 5-Hydroxymethyl-selenophen-2-carbonsaeure 1,3-Dithiolo<4,5-c>selenophene-2-thione methyl 3-amino-5-(methoxycarbonyl)selenophene-2-carboxylate tetramethyl 2,3,4,5-selenophenetetracarboxylate 2,2'-{5,5'-[5,5'-(selenophene-2,5-diyl)bis(3,4-dibutylthien-5,2-diyl)]bis-(selenophene-5,2-diyl)}bis(methan-1-yl-1-ylidene)dimalononitrile 2-(2-bromoethylsulfonyl)selenophene 2-(4,4-bis(methoxymethyl)-7-(selenophen-2-yl)hepta-1,6-diynyl)selenophene cyclopenta[c]selenophene-(CH2OMe)2 2-[5,5-Bis(methoxymethyl)-3-thiophen-2-yl-4,6-dihydrocyclopenta[c]selenophen-1-yl]thiophene 3,6-dimethylselenolo<3,2-b>selenophene 2,5-Bis(2-selenienyl)furan tetramethyl-selenophene 2,3,4-trimethyl-selenophene 2,3,5-trimethyl-selenophene selenophen-2-yl-methanol 1-selenophen-2-yl-ethanol 2-carbomethoxyselenophene