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2-(Hydroxymethyl)-6,7-ethylenedithio-tetrathiafulvalene | 142059-40-3

中文名称
——
中文别名
——
英文名称
2-(Hydroxymethyl)-6,7-ethylenedithio-tetrathiafulvalene
英文别名
[2-(5,6-Dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidene)-1,3-dithiol-4-yl]methanol
2-(Hydroxymethyl)-6,7-ethylenedithio-tetrathiafulvalene化学式
CAS
142059-40-3
化学式
C9H8OS6
mdl
——
分子量
324.558
InChiKey
LHFYPTWJYYBNIZ-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):
    2.9
  • 重原子数:
    16
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    172
  • 氢给体数:
    1
  • 氢受体数:
    7

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 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:
    2-(Hydroxymethyl)-6,7-ethylenedithio-tetrathiafulvalene 在 selenium(IV) oxide 作用下, 以 1,4-二氧六环 为溶剂, 以61%的产率得到2-Formyl-6,7-(ethane-1,2-diyldisulfanyl)tetrathiafulvalene
    参考文献:
    名称:
    四硫富瓦烯的第一烯丙基醇衍生物。通往新的共价链接的供体的途径
    摘要:
    描述了衍生自TTF的第一烯丙基醇。他们提供了新的多级氧化还原组件(6-8),包括第一个同时包含EDT-TTF和二茂铁部分的系统(6a)。
    DOI:
    10.1016/0040-4039(95)00749-3
  • 作为产物:
    描述:
    Methyl 2-(5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidene)-5-(hydroxymethyl)-1,3-dithiole-4-carboxylate六甲基磷酰三胺 、 lithium bromide 作用下, 以45%的产率得到2-(Hydroxymethyl)-6,7-ethylenedithio-tetrathiafulvalene
    参考文献:
    名称:
    2-Mono or 2,3-Bis(hydroxymethyl)-6,7-ethylenedithio-tetrathiafulvalenes: New potential precursors of organic metals endowed with hydrogen bonds
    摘要:
    The syntheses of new pi-unsymmetrical donors of the TTF family having half moiety of bis(ethylenedithio)-TTF (BEDT-TTF) and half moiety of TTF substituted with one (or two) hydroxymethyl group(s) are described. Their good pi-donating ability is demonstrated by cyclic voltammetry.
    DOI:
    10.1016/s0040-4039(00)79057-5
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文献信息

  • The first allylic alcohol derivatives of tetrathiafulvalene. A route to new covalently linked donors
    作者:Raquel Andreu、Javier Garín、Jesús Orduna、María Savirón、Santiago Uriel
    DOI:10.1016/0040-4039(95)00749-3
    日期:1995.6
    The first allylic alcohols derived from TTF are described. They afford new multi-stage redox assemblies (6–8), including the first system containing both EDT-TTF and ferrocene moieties (6a).
    描述了衍生自TTF的第一烯丙基醇。他们提供了新的多级氧化还原组件(6-8),包括第一个同时包含EDT-TTF和二茂铁部分的系统(6a)。
  • Synthesis and characterization of functionalized ethylenediselenotetrathiafulvalenes: A comparative study with their all-sulfur analogues
    作者:Javier Garín、Jesús Orduna、María Savirón、Martin R. Bryce、Adrian J. Moore、Vincent Morisson
    DOI:10.1016/0040-4020(96)00624-2
    日期:1996.8
    The synthesis of the first monofunctionalized and some new difunctionalized ethylenediseleno-TTF (EDS-TTF) derivatives is described, including systems with alcohol, ester and aldehyde substituents. The mass spectrometric behaviour of these compounds has been studied for the first time and a comparative electrochemical study with their all-sulfur analogues has been carried out.
    描述了第一个单官能化的和一些新的双官能化的乙烯二硒代-TTF(EDS-TTF)衍生物的合成,包括具有醇,酯和醛取代基的体系。首次对这些化合物的质谱行为进行了研究,并对其全硫类似物进行了电化学比较研究。
  • 2-Mono or 2,3-Bis(hydroxymethyl)-6,7-ethylenedithio-tetrathiafulvalenes: New potential precursors of organic metals endowed with hydrogen bonds
    作者:Ph. Blanchard、M. Sallé、G. Duguay、M. Jubault、A. Gorgues
    DOI:10.1016/s0040-4039(00)79057-5
    日期:1992.5
    The syntheses of new pi-unsymmetrical donors of the TTF family having half moiety of bis(ethylenedithio)-TTF (BEDT-TTF) and half moiety of TTF substituted with one (or two) hydroxymethyl group(s) are described. Their good pi-donating ability is demonstrated by cyclic voltammetry.
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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 [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)- (四甲基硫)四硫富瓦烯 2,3,6,7-tetrakis[2-(2-methoxyethoxy)ethylsulfanyl]tetrathiafulvalene 2,3-bis[2-(2-methoxyethoxy)ethylsulfanyl]-6,7-bis(methylsulfanyl)tetrathiafulvalene (5S,6S,5'S,6'S)-5,5',6,6'-tetramethyl-bis(ethylenedithio)tetrathiafulvalene 2,5-bis(4,5-ethylenedithio-1,3-dithiol-2-ylidene)-1,3,4,6-tetrathiapentalene 2,3,6,7-Tetrakis(1-octyloxymethyl)tetrathiafulvalene 2,3,6,7-Tetrakis(1-dodecyloxymethyl)tetrathiafulvalene 2,3,6,7-Tetrakis(1-pentyloxymethyl)tetrathiafulvalene 2,3,6,7-Tetrakis(1-hexyloxymethyl)tetrathiafulvalene 2,3,6,7-Tetrakis(1-propoxymethyl)tetrathiafulvalene 2,3,6,7-Tetrakis(1-decyloxymethyl)tetrathiafulvalene 2,3,6,7-Tetrakis(1-heptyloxymethyl)tetrathiafulvalene 2,6-bis(thioacetopentadecylamido)-3,7-bis(methylthiotetrathiafulvalene) 2,7-bis(thioacetopentadecylamido)-3,6-bis(methylthiotetrathiafulvalene) ethane 1,2-dithiol 2,3,6,7-Tetrakis(1-tetradecyloxymethyl)tetrathiafulvalene 2-Isopropyliden-1,3-dithiol-4,5-dicarbonitril 4,5-bis(butylthio)tetrathiafulvalene 2,3-dicyano-6,7-bis(butylthio)tetrathiafulvalene Tetrabutylammonium-(3-thioxo-3H-1,2-dithiol-5-thiolat) 5,6-dihydro-5-dimethoxymethyl-2-(5',6'-dihydro-1,3-dithiolo[4,5-b]-1,4-dithiin-2'-ylidene)-1,3-dithiolo[4,5-b]-1,4-dithiin 3H-1,2-dithiole 2,2'-(But-2-en-1,4-diyliden)bis[1,3-dithiol-4,5-dicarbonitril] 3-methylsulfanyl-[1,2]dithiolylium; iodide 2,2'-(Dodeca-2,4,6,8,10-pentaen-1,12-diyliden)bis[1,3-dithiol-4,5-dicarbonitril] (E,E)-1,6-bis[4,5-bis(methylsulfanyl)-1,3-dithiol-2-ylidene]hexa-2,4-diene