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8,9-Dihydroacenaphtho<1,2-b><1,4>dithiine | 159791-37-4

中文名称
——
中文别名
——
英文名称
8,9-Dihydroacenaphtho<1,2-b><1,4>dithiine
英文别名
1,2-ethylenedithioacenaphthylene;11,14-Dithiatetracyclo[7.6.1.05,16.010,15]hexadeca-1,3,5(16),6,8,10(15)-hexaene
8,9-Dihydroacenaphtho<1,2-b><1,4>dithiine化学式
CAS
159791-37-4
化学式
C14H10S2
mdl
——
分子量
242.365
InChiKey
CGALRKANEORZEM-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):
    3.9
  • 重原子数:
    16
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    50.6
  • 氢给体数:
    0
  • 氢受体数:
    2

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:
    8,9-Dihydroacenaphtho<1,2-b><1,4>dithiine2,3-二氯-5,6-二氰基-1,4-苯醌 作用下, 以 1,4-二氧六环 为溶剂, 以56%的产率得到Acenaphtho<1,2-b><1,4>dithiine
    参考文献:
    名称:
    7,10-二硫代氟蒽及其阳离子自由基盐
    摘要:
    通过a庚烯酮乙二硫缩醛的扩环反应,由a庚烯酮分三步制备了第一个7,10-二硫代氟代蒽。它被证明是良好的π供体和形式高传导阳离子自由基盐,与PF 6 - 。盐的X射线晶体学分析显示供体的柱状堆叠结构,并且盐在室温下显示出高电导率。
    DOI:
    10.1016/0040-4039(94)88223-1
  • 作为产物:
    描述:
    参考文献:
    名称:
    7,10-二硫代氟蒽及其阳离子自由基盐
    摘要:
    通过a庚烯酮乙二硫缩醛的扩环反应,由a庚烯酮分三步制备了第一个7,10-二硫代氟代蒽。它被证明是良好的π供体和形式高传导阳离子自由基盐,与PF 6 - 。盐的X射线晶体学分析显示供体的柱状堆叠结构,并且盐在室温下显示出高电导率。
    DOI:
    10.1016/0040-4039(94)88223-1
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文献信息

  • Hiroyuki Tani, Yoshihiro Kawada, Nagao Azuma, Noboru Ono, Tetrahedron Lett, 35 (1994) N 38, S 7051- 7054
    作者:Hiroyuki Tani, Yoshihiro Kawada, Nagao Azuma, Noboru Ono
    DOI:——
    日期:——
  • New π-electron donor systems based on acenaphtho[1,2-b][1,4]dithiine
    作者:Martin R. Bryce、Antony Chesney、Alexander K. Lay、Andrei S. Batsanov、Judith A. K. Howard
    DOI:10.1039/p19960002451
    日期:——
    Syntheses of the acenaphtho[1,2-b] [1,4] dithiine derivatives 12, 25 and 29 are reported. Cyclic voltammetric studies reveal that these compounds undergo reversible single-electron oxidations at < 1.0 V, vs. Ag/AgCl. Lithiation of compound 12 with BuLi (2 equiv.) followed by addition of either methyl iodide or ethyl chloroformate yielded the unstable ring-opened acetylene derivatives 22a and 22b, respectively. A new synthesis of 1,2-diselenine derivative 33 is reported. Compound 25 formed 1:1 charge-transfer complexes with 7,7,8,8-tetracyano-p-quinodimethane (TCNQ) and with 2,5-dibromo-TCNQ, both of which were electrical insulators. The X-ray crystal structures of compound 25, a charge-transfer complex 25:Br,TCNQ (1:1 stoichiometry) and compound 33 are reported. In the structure of 25:Br,TCNQ, molecules of 25 and Br,TCNQ form mixed stacks. The folding of the donor along the S ... S vector in the complex is 17 degrees (ef. 48 degrees in pure 25) and the conformation of 25 is discussed in the light of previous studies on 1,4-dithiine derivatives. An interesting feature of the crystal structure of 33 is the formation of pseudo-dimers with two short intermolecular Se Se contacts.
  • 7,10-dithiafluoroanthene and its cation radical salt
    作者:Hiroyuki Tani、Yoshihiro Kawada、Nagao Azuma、Noboru Ono
    DOI:10.1016/0040-4039(94)88223-1
    日期:1994.9
    The first 7,10-Dithiafluoroanthene has been prepared from acenaphthenone in three steps, via ring expansion reaction of acenaphthenone ethylenedithioacetal. It was shown to be good π-donor and form highly conducting cation radical salts with PF6−. X-ray crystallographic analysis of the salt showed columnar stack structure of donors and the salt showed high electrical conductivity at room temperature
    通过a庚烯酮乙二硫缩醛的扩环反应,由a庚烯酮分三步制备了第一个7,10-二硫代氟代蒽。它被证明是良好的π供体和形式高传导阳离子自由基盐,与PF 6 - 。盐的X射线晶体学分析显示供体的柱状堆叠结构,并且盐在室温下显示出高电导率。
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同类化合物

苊烯八醇 苊烯-1-甲醛 苊烯 苊并[3,4-d][1,3]噻唑 氘代二氢萘 全氟苊 乙酮,1-[2-(1-吡咯烷基)-1-苊烯基]- 7H-苊并[4,5-d]咪唑 5-溴苊烯 5-氟苊烯 5,6-二溴苊烯 2-氯苊烯-1-甲醛 2-偶氮基苊烯-1-醇 1-氰基苊 1-(4-甲氧基苯基)苊 1-(1-萘基)苊 1-(4-Pentenyl)acenaphthylene 1-Allylacenaphthylene 1-Methylsulfanyl-2-(prop-1-ynylsulfanyl)acenaphthylene 1,2-di(2-thienyl)acenaphthylene 1-(2-cyanophenyl)acenaphthylene 3235-acenaphthylene)Ru3(CO)7 5-hydroxymethylacenaphthylene 4-Vinylacenaphtylen 1-Chloroacenaphtho[1,2-d]-2,1,5-oxatellurazole 5-acenaphthylene boronic acid 1,1'-biacenaphthylene Pd-PEPPSI-IPrAn (dpp-BIAN)Mg(THF)3 5-ethynylacenaphthylene 4-Methyl-acenaphthylen Heptafluor-3-methoxy-acenaphthylen Acenaphthylen-5-OL 4-Chlor-acenaphthylen 4-Acenaphthylenamine diethyl (3S,4R,9S,10R)-21-oxohexacyclo[10.7.1.13,10.14,9.02,11.016,20]docosa-1(19),2(11),5,7,12,14,16(20),17-octaene-3,10-dicarboxylate 5-Acenaphthylenecarbonitrile trans-7,8-Dihydroxy-7,8-dihydrofluoranthene 5-Acenaphthylenamine anti-8,17-dimethylacenaphthyleno[1,2-a]-10-thia[2,3]metacyclophan-1-ene anti-8,16-dimethylacenaphthyleno[1,2-a][2,3]metacyclophan-1-ene 1,2-dibromo-4,7-dichloro-5,6-bis(dimethylamino)acenaphthylene 1,2,4-tribromo-6-dimethylamino-5-methylamino-acenaphthylene 1,2-dibromo-5,6-bis(dimethylamino)acenaphthylene 5,6-dimethylacenaphthylene 1-phenyl-2-propylacenaphthylene [1,2-2H]-acenaphthylene 5-Benzolsulfonylamino-acenaphthylen 1,3-bis(2,6-diisopropylphenyl)acenaphthoimidazol-2-ylidene 7,9-dihydrocyclopentacenaphthylen-8-one