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2-(5,6-二氢-1,3-二硫环戊并[4,5-B][1,4]二烷-2-亚基)-5,6-二氢-1,3-二硫环戊并[4,5-B][1,4]二烷 | 120120-58-3

中文名称
2-(5,6-二氢-1,3-二硫环戊并[4,5-B][1,4]二烷-2-亚基)-5,6-二氢-1,3-二硫环戊并[4,5-B][1,4]二烷
中文别名
——
英文名称
bis(ethylenedioxy)tetrathiafulvalene
英文别名
[bis(ethylenedioxo)tetrathia]fulvalene;bis(ethylendioxy)-tetrathiafulvalene;bis(ethylenedioxo)tetrathiafulvalene;BEDO-TTF;BEDO;2-(5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dioxin-2-ylidene)-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dioxine
2-(5,6-二氢-1,3-二硫环戊并[4,5-B][1,4]二烷-2-亚基)-5,6-二氢-1,3-二硫环戊并[4,5-B][1,4]二烷化学式
CAS
120120-58-3
化学式
C10H8O4S4
mdl
——
分子量
320.435
InChiKey
QFUHUWZDTBITGQ-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:
    371℃
  • 密度:
    1.78
  • 闪点:
    178℃

计算性质

  • 辛醇/水分配系数(LogP):
    2.8
  • 重原子数:
    18
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    138
  • 氢给体数:
    0
  • 氢受体数:
    8

SDS

SDS:a9d05f4f9e97a567ea36d1198d202d6b
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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

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文献信息

  • LAYERED HYBRID ORGANIC-INORGANIC PEROVSKITE MATERIALS
    申请人:IMEC VZW
    公开号:US20200152395A1
    公开(公告)日:2020-05-14
    In a first aspect, the present invention relates to a perovskite material comprising negatively charged layers alternated with and neutralized by positively charged layers; the negatively charged layers having a general formula selected from the list consisting of: L n−1 M n X 3n+1 , L n M n X 3n+2 , and L n−1 M′ n X 3n+3 , and the positively charged layers comprising: one or more organic ammonium cations independently selected from monovalent cations Q and divalent cations Q′, or a polyvalent cationic conjugated organic polymer Z, wherein Q, Q′ and Z comprise each a π-conjugated system in which at least 8 and preferably at least 10 atoms participate, L is a monovalent cation, M n are n independently selected metal cations averaging a valence of two, M′ n are n independently selected metal cations averaging a valence equal to 2+2/n, X is a monovalent anion, and n is larger than 1.
    在第一个方面,本发明涉及一种钙钛矿材料,其包括负电荷层和中和的正电荷层交替排列;负电荷层具有以下列表中选择的一般公式:Ln−1MnX3n+1、LnMnX3n+2和Ln−1M′nX3n+3,正电荷层包括:一个或多个独立选择的单价阳离子Q和双价阳离子Q′,或者一个多价阳离子共轭有机聚合物Z,其中Q、Q′和Z各自包括一个π共轭体系,其中至少有8个原子参与,L是一个单价阳离子,Mn是独立选择的平均价为二的金属阳离子,M′n是独立选择的平均价为2+2/n的金属阳离子,X是一个单价阴离子,n大于1。
  • ESR study of conductors made up of entirely organic materials: radical cation salts of tetrathiafulvalene derivatives with the monoanion of isocyanuric acid
    作者:E. I. Yudanova、A. M. Flakina、R. N. Lyubovskaya
    DOI:10.1007/s11172-009-0096-1
    日期:2009.4
    The radical cation salts of tetrathiafulvalene derivatives with the cyanuric acid monoanion were studied by the ESR method. The ESR data are consistent with the earlier obtained structural characteristics, electric conductivity, and optical properties of the studied salts.
    采用电子自旋共振(ESR)方法研究了四硫富瓦烯衍生物的自由基阳离子盐与氰尿酸单负离子的复合物。ESR数据与之前获得的研究盐的结构特征、电导率和光学性质一致。
  • Synthesis of Some New Electron π-Donors Containing Methoxy Groups
    作者:G. A. Mousdis、G. C. Papavassiliou、N. Psaroudakis、G. C. Anyfantis
    DOI:10.1515/znb-2004-0716
    日期:2004.7.1
    The synthesis of some new electron π-donors carrying four or two methoxy groups is described. The precursor 5,6-dimethoxy-5,6-dihydro[1,3]dithiolo[4,5-b] [1,4]dithiin- 2-thione was synthesized and by coupling reactions the symmetrical 5,6,5’,6’-tetramethoxy-5,6,5’,6’-tetrahydro- [2,2’]bi[[1,3]dithiolo[4,5-b][1,4]dithiinylidene] and unsymmetrical 5,6-dimethoxy-5,6,5’,6’-tetrahydro-[2,2’]bi[[1,3]- dithiolo[4
    描述了一些带有四个或两个甲氧基的新电子 π 供体的合成。合成了前体 5,6-二甲氧基-5,6-二氢[1,3]二硫醇[4,5-b][1,4]二硫因-2-硫酮,并通过偶联反应生成了对称的 5,6,5' ,6'-四甲氧基-5,6,5',6'-四氢-[2,2']bi[[1,3]dithiolo[4,5-b][1,4]二亚硫基]和不对称的5, 6-二甲氧基-5,6,5',6'-四氢-[2,2']双[[1,3]-二硫醇[4,5-[1,4]二亚硫基], 2-(5,6 -二甲氧基-5,6-二氢-[1,3]二硫醇[4,5-b][1,4]二噻英-2-亚基)-5,6-二氢-[1,3]二硫醇[4,5] -b][1,4]-二恶英和(5,6-二甲氧基-5,6-二氢-[1,3]二硫醇[4,5-b][1,4]二噻英-2-亚基)-6 ,7-二氢-5H-[1,3]二硫并[4,5-b][1,4]二硫平供体被制备。它们已通过光谱
  • Unsymmetrically Substituted Ethylenedioxytetrathiafulvalenes
    作者:Takehiko Mori、Hiroo Inokuchi、Aravinda M. Kini、Jack M. Williams
    DOI:10.1246/cl.1990.1279
    日期:1990.8
    Seven new electron donors, 4,5-ethylenedioxytetrathiafulvalenes where 4′,5′-substituents are trimethylenedithio, ethylenedithio, methylenedithio, 2-oxatrimethylenedithio, methylthio, hydrogen and methyl carboxylate, are prepared, and their electrochemical properties are investigated.
    制备了七种新的电子供体--4,5-亚乙二氧基四硫杂戊烯,其中 4′,5′-取代基为三亚甲基二硫、亚乙基二硫、亚甲基二硫、2-氧杂三亚甲基二硫、甲硫基、氢和羧酸甲酯。
  • Ethylenedithio(ethylenedioxo)diselenadithiafulvalene (TOST) and ethylenediseleno(ethylenedioxo)tetrathiafulvalene (SO): new unsymmetrical π-donors containing three elements in Group 16 (O, S, and Se)
    作者:Tatsuro Imakubo、Yoshinori Okano、Hiroshi Sawa、Reizo Kato
    DOI:10.1039/c39950002493
    日期:——
    The synthesis and characterization of new unsymmetrical bis(ethylenedithio)tetrathiafulvalene (ET) analogues ethylenedithio(ethylenedioxo)diselenadithiafulvalene (TOST) and ethyl enediseleno(ethylenedioxo)tetrathiafulvalene (SO) that contain three elements in group 16(O, S and Se) and their cation radical salts are reported.
    新型不对称双(亚乙基二硫代)四硫富瓦烯(ET)类似物的合成和表征,亚乙基二硫(亚乙基二氧代)二亚硒二硫富瓦烯(TOST)和乙基烯二烯丙基(亚乙基二氧代)四硫富富瓦烯(SO),它们在第16组(O,S和Se)中包含三个元素报道了阳离子自由基盐。
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同类化合物

环丙羧酸,2-(羟甲基)-3-甲基-,甲基酯,(1S,2R,3R)- 丙酸,2-甲氧基-,1-(5,6-二氢-1,4-二噁烷-2-基)-2-甲氧基-1-丙烯基酯 三丁基(5,6-二氢-1,4-二恶英-2-基)-锡烷 [1,2]二恶英并[4,3-b]吡啶 5-乙酰基-3,6-二甲基-1,4-二恶英-2(3H)-酮 5-(5,6-二氢-1,4-二氧杂环己烯-2-基)-1,3,4-噁二唑-2-胺 5,6-二氢-[1,4]二恶英-2-羧酸 5,6-二氢-1,4-二恶英-2-甲醛 5,6-二氢-1,4-二恶英-2-甲酰氯 3-甲基-5,6-二氢-1,4-二恶英-2-羧酸 2-甲基-5,6-二氢-1,4-二恶英 2-(5,6-二氢-1,4-二氧-2-基)-4,4,5,5-四甲基-1,3,2-二氧杂硼烷 2-(5,6-二氢-1,3-二硫环戊并[4,5-B][1,4]二烷-2-亚基)-5,6-二氢-1,3-二硫环戊并[4,5-B][1,4]二烷 2,3-二氢-5,6-二甲基-1,4-二恶英 2,2,2-三氟-1-(3-甲基-5,6-二氢-1,4-二恶英-2-基)乙酮 1H,5H-环戊二烯并[5,6][1,4]二恶英并[2,3-d]咪唑 1,4-二氧杂-2-己烯 1,4-二恶英-2-甲酰氯,5,6-二氢-3-甲基-(9CI) 1,4-二恶英 EDO-S,S-DMEDT-TTF 2,3-di(furan-2-yl)-5,6-dihydro-1,4-dioxine 2-(carboxymethyl)-3-(3-oxobutyl)dioxene 2-(carboxymethyl)-trans-5,6-diethyl-3-(3-oxobutyl)dioxene trifluoromethyl dihydro-1,4-dioxin-3-carbonyl chloride 6-bromo-2,3-dihydrobenzo[1,4]dioxine 3,4-(vinylenedioxy)thiophene ethyl 5,6-dihydro-2-trifluoromethyl-1,4-dioxin-3-carboxylate 5,6-dihydro-2-trifluoromethyl-1,4-dioxin-3-carboxylic acid F-2-methyl-2,3-dihydro-1,4-dioxin Phosphorodithioic acid, O,O-diethyl S-(5,6-dihydro-1,4-dioxin-2-yl) ester 2-[4,5-bis(ethylthio)-1,3-dithiol-2-ylidene]-5-(4,5-ethylenedioxy-1,3-dithiol-2-ylidene)-1,3,4,6-tetrathiapentalene Δ1(7)-8,11-dioxabicyclo<5.4.0>undecene 8-ethoxy-2,5-dioxa-7,10-dithiabicyclo<4.4.0>deca-1(6)-ene 2,2,5,5,8,8-Hexamethyl-2,3,5,6,7,8-hexahydro-benzo[1,4]dioxine ethylenedioxytetrathiafulvalenoquinone-1,3-diselenolemethide 1-(5,6-dihydro-[1,4]dioxin-2-yl)-2-isopropyl-propenone 6,7-Dimethyl-2,3-dihydro-1,4-benzodioxine-5,8-dione 3-chlorobenzo[b]fur[3,2-e][1,4]dioxin-2(9aH)-one 4,5-dimethyl-4',5'-ethylenedioxy-2,2'-ethanediylidenebis(1,3-dithiole) 4,5-bis(methylthio)-4',5'-ethylenedioxy-2,2'-ethanediylidenebis(1,3-dithiole) dioxinone 3-(5,6-Dihydro-[1,4]dioxin-2-yl)-cyclohexanone 4,5-ethylenedioxy-4'-methyltetrathiafulvalene (5,6-dihydro-p-dioxin-2-yl)phenylphosphinic acid hexachloro-2,3-dihydro-1,4-dioxin 6,7-Bis(octadecylsulfanyl)-2,3-dihydro-1,4-benzodioxine-5,8-dione 5,6-di-n-octylthio-2,3-ethylenedioxy-1,4-benzoquinone 6-Octadecylsulfanyl-2,3-dihydro-1,4-benzodioxine-5,8-dione 5-n-octylthio-2,3-ethylenedioxy-1,4-benzoquinone 6,7-Bis(dodecylsulfanyl)-2,3-dihydro-1,4-benzodioxine-5,8-dione