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1,4-dithiin | 290-79-9

中文名称
——
中文别名
——
英文名称
1,4-dithiin
英文别名
1,4-dithiine
1,4-dithiin化学式
CAS
290-79-9
化学式
C4H4S2
mdl
——
分子量
116.208
InChiKey
AKAIWNDBVZJOAJ-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

  • LogP:
    1.880 (est)

计算性质

  • 辛醇/水分配系数(LogP):
    1.3
  • 重原子数:
    6
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    50.6
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:574e3b31159c1f9ebd717413b4713fc4
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反应信息

  • 作为反应物:
    描述:
    1,4-dithiin 在 S-tosylsulfene chloride 、 sodium sulfide 作用下, 以 氯仿甲醇 为溶剂, 反应 1.5h, 生成 1,2:4,5-diepithio-3,6-dithiacyclohexane
    参考文献:
    名称:
    ALICYCLIC COMPOUND FOR OPTICAL MATERIAL
    摘要:
    公开号:
    EP1398317B1
  • 作为产物:
    描述:
    1,4-二硫-2,5-二醇氯化亚砜 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 2.0h, 以81%的产率得到1,4-dithiin
    参考文献:
    名称:
    Selective Metalations of 1,4-Dithiins and Condensed Analogues Using TMP-Magnesium and -Zinc Bases
    摘要:
    TMPMgCl center dot LiCl and TMPZnCl center dot LiCl allow facile magnesiation and zincation, respectively, of the 1,4-dithiin scaffold, producing polyfunctionalized 1,4-dithiins A subsequent metalation of these S-heterocycles can also be achieved with the same TMP bases, leading to 2,3-disubstituted-1,4-dithiins. The Mg- and Zn-TMP bases allow as well the successful metalation of 1,4,5,8-tetrathianaphthalene and 1,4,5,6,9,10-hexathiaanthracene.
    DOI:
    10.1021/acs.orglett.6b03539
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文献信息

  • Cobalt-Catalyzed Electrophilic Aminations with Anthranils: An Expedient Route to Condensed Quinolines
    作者:Jie Li、Eric Tan、Niklas Keller、Yi-Hung Chen、Peter M. Zehetmaier、Andreas C. Jakowetz、Thomas Bein、Paul Knochel
    DOI:10.1021/jacs.8b11466
    日期:2019.1.9
    The reaction of various organozinc pivalates with anthranils provides anilines derivatives, which cyclize under acidic conditions providing condensed quinolines. Using alkenylzinc pivalates, electron-rich arylzinc pivalates or heterocyclic zinc pivalates produces directly the condensed quinolines of which several structures belong to new heterocyclic scaffolds. These N-heterocycles are of particular
    各种有机锌新戊酸酯与邻氨基苯甲酸酯的反应提供苯胺衍生物,其在酸性条件下环化提供缩合喹啉。使用烯基新戊酸锌、富电子芳基新戊酸锌或杂环新戊酸锌直接产生稠合喹啉,其中几种结构属于新的杂环支架。由于具有最佳的空穴能带排列和大的带隙,这些 N-杂环特别适用于有机发光二极管,因为它们具有高光致发光量子产率和长激子寿命,以及甲基铵碘化铅钙钛矿太阳能电池中的空穴传输材料.
  • Photosensitive 1:1 Adduct between Bis(1,2-diphenyl-1,2-ethylenedithiolato)nickel(0) and Quadricyclane
    作者:Masatsugu Kajitani、Midori Kohara、Tomoko Kitayama、Yoshihiko Asano、Akira Sugimori
    DOI:10.1246/cl.1986.2109
    日期:1986.12.5
    Bis(1,2-diphenyl-1,2-ethylenedithiolato)nickel(0) (1a) reacts with quadricyclane (Q) to give a 1:1 adduct which has the same structure as that of the adduct between 1a and norbornadiene (NBD). Q reacts with 1a much faster than NBD. The adduct is thermally stable but photosensitive to dissociate into 1a and NBD.
    双(1,2-二苯基-1,2-亚乙基二硫醇基)镍(0) (1a) 与四环烷 (Q) 反应生成 1:1 加合物,其结构与 1a 和降冰片二烯 (NBD) 之间的加合物结构相同)。Q 对 1a 的反应比 NBD 快得多。该加合物是热稳定的,但光敏可分解成 1a 和 NBD。
  • Thermal and photochemical reactions of 1,4-dithiine and derivatives
    作者:Klaus Gollnick、Herta Hartmann
    DOI:10.1016/s0040-4039(00)87421-3
    日期:1982.1
    dienophiles in [2 + 4] - cycloadditions. Photochemically, they afford [2 + 4] - cyclodimerization products in the absence of oxygen; in its presence, they are degraded to CO2 and H2S among ther photooxidation products. CT-complexes occur with tetracyanoethylene, maleic anhydrides and acetylenes, but no stable products are formed, neither thermally nor photochemically.
    在热方面,二硫烷可以在[2 + 4]-环加成中作为亲二烯体反应。光化学上,他们在没有氧气的情况下提供[2 + 4]-环二聚产物;在它的存在,它们被降解为CO 2和H 2疗法光氧化产物中S上。CT配合物与四氰基乙烯,马来酸酐和乙炔一起出现,但没有形成稳定的产物,无论是热化学还是光化学方法都没有。
  • Synthesis and characterization of tetrathiatetraasterane
    作者:Nina V. Bojkova、Richard S. Glass
    DOI:10.1016/s0040-4039(98)02062-0
    日期:1998.12
    Irradiation of 1,4-dithiin gives the cis, syn, cis-photodimer in 70–80% yield whose structure has been unequivocally established by X-ray crystallographic methods. A minor product is formed in this photodimerization which is shown to be the trans, anti, trans-photodimer by X-ray structural analysis. Irradiation of the syn photodimer produces tetrathiatetraasterane in 70% yield. The structure of this
    辐照1,4-二硫氨酸可以得到70-80%的顺式,顺式,顺式二聚体,其结构已通过X射线晶体学方法明确确定。在该光二聚作用中形成次要产物,其通过X射线结构分析显示为反式,反式,反式-二聚体。合成光二聚体的辐射产生四硫四丁烷,产率为70%。该产品的结构也已通过X射线方法证明。
  • Unsaturated Thiacrown Ethers:  Synthesis, Physical Properties, and Formation of a Silver Complex
    作者:Takahiro Tsuchiya、Toshio Shimizu、Nobumasa Kamigata
    DOI:10.1021/ja0102742
    日期:2001.11.1
    wavelengths by changing the solvent from acetonitrile to cyclohexane. The cyclic voltammograms of 4-8 indicate that the larger unsaturated thiacrown ethers were oxidized more easily than the smaller systems, and unsaturated thiacrown ethers were oxidized more easily than corresponding saturated systems. The reaction of 4 with silver trifluoroacetate in acetone afforded the colorless complex Ag(I)(C2H2S)5(CF3COO)
    6-, 9-, 12-, 15-, 18-, 21-, 24-, 和 27-元不饱和硫杂环丙醚 1-8 是通过顺式 1,2-二氯乙烯与硫化钠在乙腈中反应形成的。4-8 的晶体结构通过 X 射线晶体学确定,发现 5-8 的所有硫原子都指向环的内部(内齿状)。所有的 ORTEP 图纸都显示这些分子中有空腔,4-8 中的空腔尺寸分别为 1.76、2.34、3.48、4.43 和 5.36 A。4-8 的紫外光谱显示在乙腈中 255-276 nm 范围内的吸收最大值,并且发现 4-8 的吸收最大值通过将溶剂从乙腈改变为环己烷而转移到更长的波长。4-8 的循环伏安图表明较大的不饱和噻冠醚比较小的系统更容易氧化,和不饱和的噻冠醚比相应的饱和体系更容易氧化。4与三氟乙酸银在丙酮中反应得到无色配合物Ag(I)(C2H2S)5(CF3COO)9。X射线分析确定9的晶体结构,发现5个硫原子中的3个与银原子结合。
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同类化合物

提亚鲁布林A 乙烯基 3-硝基-2,5-二苯基-1,4-二噻英 3,6-二苯基二噻英 2-溴-5-硝基-3,6-二苯基-1,4-二噻英 2-乙烯基-4H-1,3-二噻英 2-[4-(6-丙-1-炔基二噻英-3-基)丁-1,3-二炔基]环氧乙烷 2,5-二苯基-1,4-二噻英 2,5-二溴-3,6-二苯基-1,4-二噻英 2,3-二硫杂二环[2.2.2]辛-5-烯 2,3,5,6-四氰基-[1,4]-二噻硫 1,2-二硫杂-4,5-二甲基-4-环己烯 1,2-二噻英-3,6-二胺 [1,4]dithiin-1,4-dioxide 3,6-dihydro-3-methyl-1,2-dithiin (+/-)-diborn-2-eno<2,3-c;3',2'-e><1,2>dithiine 4,5-dimethyl-3H,6H-1,2-dithiin 1-oxide 3,6-bis<(isobutyryloxy)methyl>-1,2-dithiin 3,6-bis<<(cyclopropylcarbonyl)oxy>methyl>-1,2-dithiin 3-<<(cyclopentylcarbonyl)oxy>methyl>-6-(hydroxymethyl)-1,2-dithiin 3-<(acetyloxy)methyl>-6-(hydroxymethyl)-1,2-dithiin 3-<<(cyclopropylcarbonyl)oxy>methyl>-6-(hydroxymethyl)-1,2-dithiin 3,6-bis<<(cyclopentylcarbonyl)oxy>methyl>-1,2-dithiin 3,6-bis(formyl)-1,2-dithiin 3,6-bis<(acetyloxy)methyl>-1,2-dithiin 2-(2'-<3',4'-dihydro-2H-thiopyranyl>)-4H-<1,3>-dithiin 3,6-bis<(propionyloxy)methyl>-1,2-dithiin 1,2,4,5-Benzotetrathiole 1-Methyl-2,5-diphenyl-1,4-dithiin-1-ium tetrafluoroborate vinylenedithiotetrathiafulvalene 2,3,5,6-Tetramethyl-[1,4]dithiine 2,5-Diphenyl-6-bromo-3-nitro-1,4-dithiin-4-sulphoxide 3,6-Bis-(4-butyl-phenyl)-[1,2]dithiine 1,4-Dithiin-tetracarboxamid 3,6-bis(trimethylsilyl)-1,2-dithiin 3,6-di[2,3-dideoxy-α-D-erythro-hex-2-enopyranosyl]oxymethyl-1,2-dithiin 1,2,3,4,6,7,8,9-Octahydro-thianthrene ((2S,4S)-pentane-2,4-dithio)((1'R,5'R)-6',6'-dimethyl-bicyclo[3.1.1]heptene-2',3'-dithio)tetrathiafulvalene (ethylenedithio)((1R,5R)-6,6-dimethyl-bicyclo[3.1.1]heptene-2,3-dithio)tetrathiafulvalene octafluoro-2,7-dithiatricyclo<6.2.0.03,6>deca-1(8),3(6)-diene 2,5-Dimethyl-3,6-diphenyl-[1,4]dithiin 2,5-Di(t-butyl)-1,4-dithiin 2,6-di(2-thienyl)-1,4-dithiin 3,6-bis(tert-butyl)-1,2-dithiin 2,3-(2,3-dithiabutane-1,4-diyl)-6,7-bis(methylsulfanyl)tetrathiafulvalene 4-methyl-2-propenyl-4H-1,3-dithiin 2,3-dithiabicyclo<2.2.1>hept-5-ene 2,3-Bis(2-cyanoethylthio)-6,7-bis(2,3-dithiabutane-1,4-diyl)tetrathiafulvalene 3-(Acetamido)methyl-6-[(tert-butyldimethylsilyloxy)methyl]-1,2-dithiin 3-<<(tert-butyldimethylsilyl)oxy>methyl>-6-(2-cyanoethen-1-yl)-1,2-dithiin