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2,4'-bis(3",5"-di-tert-butyl-4"-hydroxyphenyl)-2'-[4"-(3''',5'''-di-tert-butyl-4-hydroxyphenyl)phenyl]-5-methyltolane | 250610-10-7

中文名称
——
中文别名
——
英文名称
2,4'-bis(3",5"-di-tert-butyl-4"-hydroxyphenyl)-2'-[4"-(3''',5'''-di-tert-butyl-4-hydroxyphenyl)phenyl]-5-methyltolane
英文别名
2,6-Ditert-butyl-4-[4-[2-[5-(3,5-ditert-butyl-4-hydroxyphenyl)-2-[2-[5-(3,5-ditert-butyl-4-hydroxyphenyl)-2-methylphenyl]ethynyl]phenyl]ethynyl]phenyl]phenol
2,4'-bis(3",5"-di-tert-butyl-4"-hydroxyphenyl)-2'-[4"-(3''',5'''-di-tert-butyl-4-hydroxyphenyl)phenyl]-5-methyltolane化学式
CAS
250610-10-7
化学式
C65H76O3
mdl
——
分子量
905.317
InChiKey
CWLQEFBZBVMNAW-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):
    20.2
  • 重原子数:
    68
  • 可旋转键数:
    13
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    60.7
  • 氢给体数:
    3
  • 氢受体数:
    3

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:
    2,4'-bis(3",5"-di-tert-butyl-4"-hydroxyphenyl)-2'-[4"-(3''',5'''-di-tert-butyl-4-hydroxyphenyl)phenyl]-5-methyltolanesodium hydroxide 、 potassium hexacyanoferrate(III) 作用下, 以 甲苯 为溶剂, 反应 0.5h, 生成
    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:
    描述:
    4-(3',5'-di-tert-butyl-4'-hydroxyphenyl)ethynyl benzene 在 sodium hydroxidecopper(l) iodide四(三苯基膦)钯三乙胺 作用下, 以 四氢呋喃甲醇 为溶剂, 反应 43.0h, 生成 2,4'-bis(3",5"-di-tert-butyl-4"-hydroxyphenyl)-2'-[4"-(3''',5'''-di-tert-butyl-4-hydroxyphenyl)phenyl]-5-methyltolane
    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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