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2,2-Dibutyl-1,3,4,7-tetrathia-2-stanna-indene | 161088-10-4

中文名称
——
中文别名
——
英文名称
2,2-Dibutyl-1,3,4,7-tetrathia-2-stanna-indene
英文别名
2,2-dibutyl-[1,3,2]dithiastannolo[4,5-b][1,4]dithiine
2,2-Dibutyl-1,3,4,7-tetrathia-2-stanna-indene化学式
CAS
161088-10-4
化学式
C12H20S4Sn
mdl
——
分子量
411.265
InChiKey
WYDHQDAYYOUCCR-UHFFFAOYSA-L
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):
    6.59
  • 重原子数:
    17.0
  • 可旋转键数:
    6.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    0.0
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

反应信息

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文献信息

  • Newly modified TTF and DSDTF donors for developing molecular-based organic metals
    作者:Jun-ichi Yamada、Hiroyuki Nishikawa、Koichi Kikuchi
    DOI:10.1039/a807698g
    日期:——
    The development of organic metals based on newly modified TTF (tetrathiafulvalene) and DSDTF (diselenadithiafulvalene) donors via the Lewis acid-promoted reactions of organotin compounds with electrophiles is described. The Me 3 Al-promoted reaction is versatile for construction of 1,3-dichalcogenol-2-ylidene moieties, and the BF 3 -promoted reaction is utilized to prepare the 1,3-dithiole-2-chalcogenone derivatives condensed with a bis-fused six-membered heterocycle. The use of these reactions enables us to synthesize DHTTF (dihydrotetrathiafulvalene) donors, DHTTF-fused donors, DSDTF donors incorporating the vinylenedithio end group, and TTF donors with an extended periphery by addition of aliphatic heterocycles. The crystal structures of radical-cation salts derived from these π-electron donors, including some new κ-type salts with a 2:1 (donor:anion) stoichiometry, are also disclosed.
    本文介绍了通过路易斯酸促进有机锡化合物与亲电体的反应,开发基于新修饰的 TTF(四噻吩戊二烯)和 DSDTF(二噻吩戊二烯)供体的有机属。Me 3 Al 促成的反应可用于构建 1,3-二羰基烯-2-亚基分子,而 BF 3 促成的反应则可用于制备与双融合六元杂环缩合的 1,3-二代-2-羰基烯酮衍生物。利用这些反应,我们可以合成 DHTTF(二氢四戊烯)供体、DHTTF-融合供体、含有乙烯末端基团的 DSDTF 供体,以及通过添加脂肪族杂环而具有扩展外围的 TTF 供体。此外,还公布了由这些π电子供体衍生的自由基阳离子盐的晶体结构,包括一些具有 2:1(供体:阴离子)化学计量的新型κ型盐。
  • New organic metals based on vinylenedithio-annulated diselenadithiafulvalene derivatives
    作者:Jun-ichi Yamada、Sh�ji Satoki、Hiroyuki Anzai、Kenji Hagiya、Masafumi Tamura、Yutaka Nishio、Koji Kajita、Emiko Watanabe、Michiko Konno、Tatsuo Sato、Hiroyuki Nishikawa、Koichi Kikuchi
    DOI:10.1039/cc9960001955
    日期:——
    The synthesis of vinylenedithio-annulated DSDTF (diselenadithiafulvalene) derivatives 1–3 and their radical cation salts are investigated, serveral of which exhibit metallic conducting behaviour.
    研究了乙烯基annulated DSDTF(二烯二戊烯)衍生物 1-3 及其自由基阳离子盐的合成,其中几种衍生物表现出属导电性。
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同类化合物

四硫杂富瓦烯-D4 四硫富瓦烯 四(戊硫代)四硫富瓦烯 四(十八烷基硫代)四硫富瓦烯 四(乙硫基)四硫富瓦烯[有机电子材料] 双(亚乙基二硫醇)四硫代富瓦烯 双(三亚甲基二硫代)四硫富瓦烯 三(四硫富瓦烯)双(四氟硼酸盐)复合物 [1,3]二噻唑并[4,5-d]-1,3-二噻唑,2,5-二(1,3-二硫醇-2-亚基)- 5-甲基二硫杂环戊烯-3-硫酮 5-氨基-3-硫代氧基-3H-(1,2)二硫杂环戊烯-4-羧酸乙酯 5-氨基-3-硫代氧基-3H-(1,2)二硫杂环戊烯-4-甲腈 5,6-二氢-4H-环戊并[1,2]二硫代-3-硫酮 4,4’,5-三甲基四硫富瓦烯 4-甲基二硫杂环戊烯-3-硫酮 4-新戊基-3H-1,2-二硫杂环戊烯-3-硫酮 4,5-二甲基-3H-1,2-二硫醇-3-酮 4,5,6,7-四氢苯并[1,2]二硫-3-硫酮 4,4’-二甲基连四硫富瓦烯 4,4,5,5,6,6,7,7-八氢二苯并四硫富瓦烯 3H-1,2-二硫杂环戊二烯-3-酮 3H-1,2-二硫杂环戊二烯-3-硫酮 2-(4,5-二甲基-1,3-二硫杂环戊烯-2-亚基)-4,5-二甲基-1,3-二硫杂环戊烯 2,3,6,7-四(2-氰乙基硫代)四硫富瓦烯 1,3-二噻唑,2-[4,5-二(癸基硫代)-1,3-二硫醇-2-亚基]-4,5-二(癸基硫代)- 1,3-二噻唑,2-[4,5-二(十四烷基硫代)-1,3-二硫醇-2-亚基]-4,5-二(十四烷基硫代)- 1,3-二噻唑,2-[4,5-二(十一烷基硫代)-1,3-二硫醇-2-亚基]-4,5-二(十一烷基硫代)- (四甲基硫)四硫富瓦烯 3-[[2-[4,5-Bis(methylsulfanyl)-1,3-dithiol-2-ylidene]-5-[3-[[2-[4,5-bis(methylsulfanyl)-1,3-dithiol-2-ylidene]-5-[3-[[2-[4,5-bis(methylsulfanyl)-1,3-dithiol-2-ylidene]-5-[3-[[2-[4,5-bis(methylsulfanyl)-1,3-dithiol-2-ylidene]-5-(2-cyanoethylsulfanyl)-1,3-dithiol-4-yl]sulfanyl]propylsulfanyl]-1,3-dithiol-4-yl]sulfanyl]propylsulfanyl]-1,3-dithiol-4-yl]sulfanyl]propylsulfanyl]-1,3-dithiol-4-yl]sulfanyl]propanenitrile 4,5-Bis-{2-[2-(2-iodo-ethoxy)-ethoxy]-ethylsulfanyl}-4',5'-bis-methylsulfanyl-[2,2']bi[[1,3]dithiolylidene] 2-<4,5-bis(methylthio)-1,3-dithiol-2-ylidene>-5-(thiopyran-4-ylidene)-1,3,4,6-tetrathiapentalene 2,3-bis(2-cyanoethylthio)-6,7-bis(2-hydroxyethylthio)tetrathiafulvalene 4,5-bis(decylthio)-4'-(3-cyanopropyl)thio-5-methyltetrathiafulvalene 4,5,4',5'-Tetrakis-trimethylsilanylethynyl-[2,2']bi[[1,3]dithiolylidene] bis(Dimethylvinylenedithio)tetrathiafulvalene 2,3-Bis{2-[2-(2-chloroethoxy)ethoxy]ethylthio}-6-(2-cyanoethylthio)-7-methylthiotetrathiafulvalene 3-[5-(2-Cyano-ethylselanyl)-2-methylsulfanyl-[1,3]dithiol-4-ylselanyl]-propionitrile 2-(4-Pent-4-ynyl-[1,3]dithiol-2-ylidene)-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiine 2-(4-Nonadeca-4,6-diynyl-[1,3]dithiol-2-ylidene)-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiine 5-Trifluoromethyl-[1,2]dithiole-3-thione 4-[(trimethylsilyl)ethynyl]-5-methyl-4',5'-ethylenedithiotetrathiafulvalene [4-Methyl-5-methylsulfanyl-[1,2]dithiol-(3Z)-ylidene]-thioacetic acid S-methyl ester 1,3-Dithiolo[4,5-b][1,4]dithiin,5,6-dihydro-2-[4-(9-decynyl)-1,3-dithiol-2-ylidene]- di(vinylthio)ethylenedithiotetrathiafulvalene 2,3:8,9-Bis(ethylendithio)-1,4,7,10-tetrathiafulvalen, CT-Komplex mit 2,5-Bis(cyanimino)-2,5-dihydro-3,6-diiodthieno<3,2-b>thiophen 4-ethyl-2-isopropylidene-[1,3]dithiole 2-[1-Chloro-1-methylsulfanylcarbonyl-meth-(Z)-ylidene]-5-methylsulfanyl-[1,3]dithiole-4-carbothioic acid S-methyl ester tetra(vinylthio)tetrathiafulvalene