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六巯基三亚苯 | 100077-38-1

中文名称
六巯基三亚苯
中文别名
——
英文名称
triphenylene-2,3,6,7,10,11-hexathiol
英文别名
2,3,6,7,10,11-triphenylene-hexathiol;2,3,6,7,10,11-Triphenylenehexathiol
六巯基三亚苯化学式
CAS
100077-38-1
化学式
C18H12S6
mdl
——
分子量
420.689
InChiKey
HBSGIZZPDDQYBQ-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):
    5.8
  • 重原子数:
    24
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    6
  • 氢给体数:
    6
  • 氢受体数:
    6

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

反应信息

  • 作为反应物:
    描述:
    六巯基三亚苯 、 cobalt(II) diacetate tetrahydrate 在 ammonium hydroxide 作用下, 以 为溶剂, 反应 24.0h, 以62%的产率得到
    参考文献:
    名称:
    Porous Scaffolds for Electrochemically Controlled Reversible Capture and Release of Ethylene
    摘要:
    This Communication describes the use of porous coordination polymers (PCP) with integrated metal bis(dithiolene) units to achieve electrochemically controlled capture and release of ethylene in the solid state. Applying positive potential (+2.0 V) to these PCPs promotes ethylene capture, and subsequent dose of negative potential (-2.0 V) induces the release. These materials are resistant to poisoning by small reactive gases (CO and H2S) that may interact with embedded metallic sites.
    DOI:
    10.1021/jacs.7b08102
  • 作为产物:
    描述:
    hexasodium 2,3,6,7,10,11-triphenylenehexathiolate 在 盐酸 作用下, 以 为溶剂, 以82 mg的产率得到六巯基三亚苯
    参考文献:
    名称:
    大面积,自由站立的二维超分子聚合物单层板,可高效产生电催化氢
    摘要:
    共价或非共价有机二维纳米片的合理构造是一个引人入胜的目标,因为它们在电子,膜技术,催化,传感和能源技术中的应用前景广阔。在此,通过使用以下方法很容易制得大面积(平方毫米)和独立的二维超分子聚合物(2DSP)单层片(厚度为0.7-0.9 nm),其中包括三亚苯基稠合的双(二硫代)镍镍配合物。 Langmuir-Blodgett方法。此类2DSP对水产生氢气具有出色的电催化活性,Tafel斜率为80.5 mV·十进制-1,在10 mA cm -2下的超电势为333 mV。优于最近报道的碳纳米管负载的分子催化剂和杂原子掺杂的石墨烯催化剂。这项工作对于开发用于能源技术的新型独立有机二维材料很有希望。
    DOI:
    10.1002/anie.201506048
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文献信息

  • In situ production of silver nanoparticles on an aldehyde-equipped conjugated porous polymer and subsequent heterogeneous reduction of aromatic nitro groups at room temperature
    作者:Jie Liu、Jieshun Cui、Filipe Vilela、Jun He、Matthias Zeller、Allen D. Hunter、Zhengtao Xu
    DOI:10.1039/c5cc04476f
    日期:——

    Silver lining on porous polymer – all from heating Tollen's reagent and a polymer host deriving its versatile functions from pendant aldehyde groups and rigid thioether joints.

    多孔聚合物上的银色涂层 - 全部来自加热托伦试剂和一种聚合物宿主,其多功能性来自挂链醛基团和刚性硫醚连接。
  • [EN] POROUS SCAFFOLDS FOR ELECTROCHEMICALLY-CONTROLLED REVERSIBLE CAPTURE AND RELEASE OF ALKENES<br/>[FR] ÉCHAFAUDAGES POREUX POUR CAPTURE ET LIBÉRATION RÉVERSIBLES D'ALCÈNES À COMMANDE ÉLECTROCHIMIQUE
    申请人:DARTMOUTH COLLEGE
    公开号:WO2019032804A1
    公开(公告)日:2019-02-14
    In some embodiments, the present disclosure pertains to a method for capturing alkenes that includes: associating the alkenes with metal-organic frameworks, where the metal-organic frameworks includes one or more metals and one or more ligands coordinated with the one or more metals, and where the metal-organic frameworks are conductive; and oxidizing the metal- organic frameworks, where the oxidizing results in a capturing of the alkenes by the metal- organic frameworks. Additional embodiments of the present disclosure pertain to a system for capturing alkenes that includes: metal-organic frameworks, where the metal-organic frameworks include one or more metals and one or more ligands coordinated with the one or more metals, and where the metal-organic frameworks are conductive; and an alkene feed source associated with the metal-organic frameworks, where the alkene feed source is configured to deliver an alkene feed to the system.
    在某些实施例中,本公开涉及一种捕获烯烃的方法,包括:将烯烃与金属有机框架相结合,其中金属有机框架包括一个或多个金属和一个或多个与一个或多个金属配位的配体,并且金属有机框架是导电的;以及氧化金属有机框架,其中氧化导致金属有机框架捕获烯烃。本公开的其他实施例涉及一种用于捕获烯烃的系统,包括:金属有机框架,其中金属有机框架包括一个或多个金属和一个或多个与一个或多个金属配位的配体,并且金属有机框架是导电的;以及与金属有机框架相关联的烯烃进料源,其中烯烃进料源被配置为向系统输送烯烃进料。
  • Metallic Conductivity in a Two-Dimensional Cobalt Dithiolene Metal–Organic Framework
    作者:Andrew J. Clough、Jonathan M. Skelton、Courtney A. Downes、Ashley A. de la Rosa、Joseph W. Yoo、Aron Walsh、Brent C. Melot、Smaranda C. Marinescu
    DOI:10.1021/jacs.7b05742
    日期:2017.8.9
    a great deal of attention due to their relatively high charge carrier mobility and low resistivity. Here we report on the temperature-dependent charge transport properties of a 2D cobalt 2,3,6,7,10,11-triphenylenehexathiolate framework. Variable temperature resistivity studies reveal a transition from a semiconducting to a metallic phase with decreasing temperature, which is unprecedented in MOFs. We
    二维(2D)金属有机框架(MOF)由于其相对较高的电荷载流子迁移率和较低的电阻率而受到了广泛的关注。在这里,我们报告2D,3、6、7、10、11-三亚苯基六硫代钴骨架的温度依赖性电荷传输性质。可变温度电阻率研究表明,随着温度的降低,从半导体相过渡到金属相,这在MOF中是前所未有的。我们发现这种转变高度依赖于膜厚度和捕获在孔中的溶剂量,电子结构的密度泛函理论计算支持了材料的复杂金属电导率。这些结果确定了第一个实验观察到的MOF,表现出带状金属导电性。
  • Multifunctional monomers containing bound mesogenic poragen forming moieties and polyarylene compositions therefrom
    申请人:Hefner E. Robert
    公开号:US20070027278A1
    公开(公告)日:2007-02-01
    A compound (monomer) comprising i) one or more dienophile groups (A-functional groups), ii) one or more ring structures comprising two conjugated carbon-to-carbon double bonds and a leaving group L (B-functional groups), and iii) one or more chemically bound mesogenic poragen forming moieties, characterized in that the A-functional group is capable of reaction under cycloaddition reaction conditions with the B-functional group to thereby form a cross-linked, polyphenylene polymer.
    一种化合物(单体),包括i)一个或多个二烯基(A-官能团);ii)一个或多个环结构,其中包括两个共轭碳-碳双键和一个离去基团L(B-官能团);和iii)一个或多个化学键合的介向原子形成基团,其特征在于A-官能团能够在环加成反应条件下与B-官能团发生反应,从而形成交联的聚苯乙烯聚合物。
  • Two-Dimensional Metal–Organic Surfaces for Efficient Hydrogen Evolution from Water
    作者:Andrew J. Clough、Joseph W. Yoo、Matthew H. Mecklenburg、Smaranda C. Marinescu
    DOI:10.1021/ja5116937
    日期:2015.1.14
    Hydrogen production through the reduction of water has emerged as an important strategy for the storage of renewable energy in chemical bonds. One attractive scenario for the construction of efficient devices for electrochemical splitting of water requires the attachment of stable and active hydrogen evolving catalysts to electrode surfaces, which remains a significant challenge. We demonstrate here the successful integration of cobalt dithiolene catalysts into a metal-organic surface to generate very active electrocatalytic cathode materials for hydrogen generation from water. These surfaces display high catalyst loadings and remarkable stability even under very acidic aqueous solutions.
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