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1,2-μ-S(4'-C6H3(CH3))S-C2B10H10 | 620986-94-9

中文名称
——
中文别名
——
英文名称
1,2-μ-S(4'-C6H3(CH3))S-C2B10H10
英文别名
——
1,2-μ-S(4'-C6H3(CH3))S-C2B10H10化学式
CAS
620986-94-9
化学式
C9H16B10S2
mdl
——
分子量
296.468
InChiKey
LAGWKGNFKQCGTJ-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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为反应物:
    描述:
    1,2-μ-S(4'-C6H3(CH3))S-C2B10H10四甲基氯化铵 在 KOH 作用下, 以 乙醇 为溶剂, 以95%的产率得到[N(CH3)4][7,8-μ-S(4'-C6H3(CH3))S-C2B9H10]
    参考文献:
    名称:
    A versatile rigid binucleating ligand for Rh2(μ-Cl)2 moieties: its application as a catalyst in hydrogenation and cyclopropanation
    摘要:
    A rigid non-deforming "MCl2M" binucleating ligand [7,8-mu-S(4'-C6H3(CH3))S-C2B9H10](-) able to held the two rhodium atoms in a cooperative distance has been synthesized. The original two bridging chlorides are retained in [Rh-2(C5Me5)(2)Cl-2{7,8-mu-S(4'C6H3(CH3))S-C2B9H10}](+). Hydrogenation of 1-hexene is 10 times faster with [Rh-2(C5Me5)(2)Cl-2{7,8-mu-S(4'-C6H3(CH3))S-C2B9H10}](+) than with [Rh-2(C5Me5)(2)Cl-4]. A hydrogenation mechanism has been proposed which assumes that [Rh-2(C5Me5)(2)(Cl)(H){7,8-mu-S(4'-C6H3(CH3))S-C2B9H10}](+) is the first generated species in the process. (C) 2003 Elsevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0022-328x(03)00204-3
  • 作为产物:
    描述:
    正丁基锂1,2-dicarba-closo-dodecaborane(12)甲苯-3,4-二硫酚 在 N-chlorosuccinimide 作用下, 以 乙醚正己烷 为溶剂, 以70%的产率得到1,2-μ-S(4'-C6H3(CH3))S-C2B10H10
    参考文献:
    名称:
    A versatile rigid binucleating ligand for Rh2(μ-Cl)2 moieties: its application as a catalyst in hydrogenation and cyclopropanation
    摘要:
    A rigid non-deforming "MCl2M" binucleating ligand [7,8-mu-S(4'-C6H3(CH3))S-C2B9H10](-) able to held the two rhodium atoms in a cooperative distance has been synthesized. The original two bridging chlorides are retained in [Rh-2(C5Me5)(2)Cl-2{7,8-mu-S(4'C6H3(CH3))S-C2B9H10}](+). Hydrogenation of 1-hexene is 10 times faster with [Rh-2(C5Me5)(2)Cl-2{7,8-mu-S(4'-C6H3(CH3))S-C2B9H10}](+) than with [Rh-2(C5Me5)(2)Cl-4]. A hydrogenation mechanism has been proposed which assumes that [Rh-2(C5Me5)(2)(Cl)(H){7,8-mu-S(4'-C6H3(CH3))S-C2B9H10}](+) is the first generated species in the process. (C) 2003 Elsevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0022-328x(03)00204-3
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