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[(Li(THF)2)2(9,10-diboraanthracene) | 1254045-95-8

中文名称
——
中文别名
——
英文名称
[(Li(THF)2)2(9,10-diboraanthracene)
英文别名
——
[(Li(THF)2)2(9,10-diboraanthracene)化学式
CAS
1254045-95-8
化学式
C28H42B2Li2O4
mdl
——
分子量
478.143
InChiKey
XJVGIYLVHKZGPZ-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

  • 作为产物:
    参考文献:
    名称:
    Dilithio 9,10-Diborataanthracene: Molecular Structure and 1,4-Addition Reactions
    摘要:
    9,10-Dihydro-9,10-diboraanthracene ([1](n)) and its SMe2 adduct 1(SMe2)(2) are readily reduced with lithium in THF to the dianionic 9,10-diborataanthracene Li-2[1]. An X-ray crystal structure analysis of (Li(thf)(2))(2)[1] revealed monomeric inverse sandwich complexes, each of them containing two Li(thf)(2) moieties coordinated to both sides of the central B2C4 ring. Compared to 9,10-dimethyl-9,10-dihydro-9,10-diboraanthracene, the four B-C-Ar bonds of (Li(thf)(2))(2)[1] are shorter by 0.046(4) angstrom, thereby indicating an increased degree of B=C-Ar double-bond character. Consequently,(Li(thf)2)2[1] reacts with 4,4' -dimethylbenzophenone as a B=C-Ar-C-Ar=B diene and undergoes a[4+2] cycloaddition reaction with formation of a bicyclic product. In contrast, tert-butylacetylene reacts with (Li(thf)(2))(2)[1]under formal 1,4-addition of its methinic C H group instead of its C C triple bond to the two boron atoms.
    DOI:
    10.1021/om100825m
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