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分子结构分类

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
925458-47-5
化学式
H3S
mdl
——
分子量
37.0739
InChiKey
RWSOTUBLDIXVET-ZSJDYOACSA-O
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):
    -0.81
  • 重原子数:
    1.0
  • 可旋转键数:
    0.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    0.0
  • 氢给体数:
    0.0
  • 氢受体数:
    0.0

反应信息

  • 作为反应物:
    描述:
    五氟化锑氟磺酸二氧化硫 为溶剂, 生成 Deuteriosulfanium
    参考文献:
    名称:
    四氢ulf盐H4S2 +:氟硫酸中的硫化氢(DH2S +)的氢-氘交换-d:五氟化锑和氟硫酸:硫化五氢中的硫化氢(D2HS +)和理论计算
    摘要:
    DOI:
    10.1021/j100315a005
  • 作为产物:
    描述:
    参考文献:
    名称:
    四氢ulf盐H4S2 +:氟硫酸中的硫化氢(DH2S +)的氢-氘交换-d:五氟化锑和氟硫酸:硫化五氢中的硫化氢(D2HS +)和理论计算
    摘要:
    DOI:
    10.1021/j100315a005
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文献信息

  • Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: S: SVol.4a/b, 1.3.8.11.2, page 214 - 216
    作者:
    DOI:——
    日期:——
  • Ion-molecule reactions in mixture of methane with water, hydrogen sulfide, and ammonia
    作者:Wesley T. Huntress、Russell F. Pinizzotto、James B. Laudenslager
    DOI:10.1021/ja00794a001
    日期:1973.6.27
  • Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: S: SVol.4a/b, 1.3.8.11.1, page 212 - 214
    作者:
    DOI:——
    日期:——
  • Ion—Molecule Reactions of Propane Ions with Benzene, 1,3—Butadiene, Hydrogen Sulfide, and Nitric Oxide
    作者:L. I. Bone、J. H. Futrell
    DOI:10.1063/1.1701638
    日期:1967.12
    Reactions of the principal primary ions from propane, C3H8+, C3H7+, C3H6+, C3H5+, C3H3+, C2H5+, C2H4+, C2H3+, and CH3+ with benzene, 1,3-butadiene, nitric oxide, and H2S were investigated in a tandem mass spectrometer. Reaction mechanisms are deduced for these systems and it is suggested that a relatively long-lived reaction complex is involved for most of these reactions. For the reaction of propyl ions with benzene an unstable adduct C9H13+ was observed which could be stabilized by collision and a unimolecular rate constant of 107sec−1 for its decomposition was estimated from its pressure dependence. In the H2S+–C3D8 and C3D8+—H2S systems charge exchange and deuteronation of H2S are competitive reactions, both proceeding via a long-lived intermediate C3D8H2S+ in which extensive isotopic exchange occurs. The results of this study are correlated with recent radiolysis experiments and it is concluded that these two methods for studing gas-phase ionic reactions are complementary.
  • Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: S: SVol.4a/b, 1.3.8.4, page 200 - 203
    作者:
    DOI:——
    日期:——
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