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3-(3',5'-di-tert-butyl-4'-hydroxyphenyl)-6-methyl-4'-[3',5'-di-tert-butyl-4'-(trimethylsilyloxy)phenyl]-tolane | 250610-05-0

中文名称
——
中文别名
——
英文名称
3-(3',5'-di-tert-butyl-4'-hydroxyphenyl)-6-methyl-4'-[3',5'-di-tert-butyl-4'-(trimethylsilyloxy)phenyl]-tolane
英文别名
2,6-Ditert-butyl-4-[4-[2-[5-(3,5-ditert-butyl-4-trimethylsilyloxyphenyl)-2-methylphenyl]ethynyl]phenyl]phenol
3-(3',5'-di-tert-butyl-4'-hydroxyphenyl)-6-methyl-4'-[3',5'-di-tert-butyl-4'-(trimethylsilyloxy)phenyl]-tolane化学式
CAS
250610-05-0
化学式
C46H60O2Si
mdl
——
分子量
673.067
InChiKey
FZMCITKPCVMDGQ-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):
    12.84
  • 重原子数:
    49
  • 可旋转键数:
    10
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    29.5
  • 氢给体数:
    1
  • 氢受体数:
    2

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:
    3-(3',5'-di-tert-butyl-4'-hydroxyphenyl)-6-methyl-4'-[3',5'-di-tert-butyl-4'-(trimethylsilyloxy)phenyl]-tolanesodium hydroxide 作用下, 以 四氢呋喃甲醇 为溶剂, 反应 4.5h, 以88%的产率得到3-(3',5'-di-tert-butyl-4'-hydroxyphenyl)-6-methyl-4'-[3',5'-di-tert-butyl-4'-hydroxyphenyl]-tolane
    参考文献:
    名称:
    Acyclic and Cyclic Di- and Tri(4-oxyphenyl-1,2-phenyleneethynylene)s:  Their Synthesis and Ferromagnetic Spin Interaction
    摘要:
    A new set of pi-conjugated and alternant but non-Kekule-type di- and tri(1,2-phenyleneethynylene)s pendantly substituted with phenoxyl radicals at the 4 positions (1a, 2a, and 3a) was synthesized. The synthesis of these acyclic and cyclic compounds was achieved through the head-to-tail coupling of a-bromo(or -iodo)-4-[3',5'-di-tert-butyl-4'-trimethylsiloxyl(or-hydroxy)phenyl]-1-ethynylbenzenes. The di- and triphenoxyl compounds (1a, and 2a and 3a) were triplet and quartet at the ground state, respectively, which was ascribed to a ferromagnetic coupling effect of the diphenyl ethynylene bridge for the pendant phenoxyls' spins. The cyclic pi-conjugation in 3a exhibited a stronger effect on the spin alignment.
    DOI:
    10.1021/jo990575i
  • 作为产物:
    参考文献:
    名称:
    Acyclic and Cyclic Di- and Tri(4-oxyphenyl-1,2-phenyleneethynylene)s:  Their Synthesis and Ferromagnetic Spin Interaction
    摘要:
    A new set of pi-conjugated and alternant but non-Kekule-type di- and tri(1,2-phenyleneethynylene)s pendantly substituted with phenoxyl radicals at the 4 positions (1a, 2a, and 3a) was synthesized. The synthesis of these acyclic and cyclic compounds was achieved through the head-to-tail coupling of a-bromo(or -iodo)-4-[3',5'-di-tert-butyl-4'-trimethylsiloxyl(or-hydroxy)phenyl]-1-ethynylbenzenes. The di- and triphenoxyl compounds (1a, and 2a and 3a) were triplet and quartet at the ground state, respectively, which was ascribed to a ferromagnetic coupling effect of the diphenyl ethynylene bridge for the pendant phenoxyls' spins. The cyclic pi-conjugation in 3a exhibited a stronger effect on the spin alignment.
    DOI:
    10.1021/jo990575i
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文献信息

  • Acyclic and Cyclic Di- and Tri(4-oxyphenyl-1,2-phenyleneethynylene)s:  Their Synthesis and Ferromagnetic Spin Interaction
    作者:Hiroyuki Nishide、Masahiro Takahashi、Junichi Takashima、Yong-Jin Pu、Eishun Tsuchida
    DOI:10.1021/jo990575i
    日期:1999.10.1
    A new set of pi-conjugated and alternant but non-Kekule-type di- and tri(1,2-phenyleneethynylene)s pendantly substituted with phenoxyl radicals at the 4 positions (1a, 2a, and 3a) was synthesized. The synthesis of these acyclic and cyclic compounds was achieved through the head-to-tail coupling of a-bromo(or -iodo)-4-[3',5'-di-tert-butyl-4'-trimethylsiloxyl(or-hydroxy)phenyl]-1-ethynylbenzenes. The di- and triphenoxyl compounds (1a, and 2a and 3a) were triplet and quartet at the ground state, respectively, which was ascribed to a ferromagnetic coupling effect of the diphenyl ethynylene bridge for the pendant phenoxyls' spins. The cyclic pi-conjugation in 3a exhibited a stronger effect on the spin alignment.
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