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2,7-bis(triisopropylsilyl)naphtho[2,3-b:6,7-b']dithiophene | 1398689-71-8

中文名称
——
中文别名
——
英文名称
2,7-bis(triisopropylsilyl)naphtho[2,3-b:6,7-b']dithiophene
英文别名
Tri(propan-2-yl)-[7-tri(propan-2-yl)silyl-[1]benzothiolo[6,5-f][1]benzothiol-2-yl]silane
2,7-bis(triisopropylsilyl)naphtho[2,3-b:6,7-b']dithiophene化学式
CAS
1398689-71-8
化学式
C32H48S2Si2
mdl
——
分子量
553.036
InChiKey
WBJFOXHAXSJXBZ-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):
    11.04
  • 重原子数:
    36
  • 可旋转键数:
    8
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    56.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    2,7-bis(triisopropylsilyl)naphtho[2,3-b:6,7-b']dithiophene联硼酸频那醇酯 在 (1,5-cyclooctadiene)(methoxy)iridium(I) dimer 、 4,4'-二叔丁基-2,2'-二吡啶 作用下, 以 环己烷 为溶剂, 以42%的产率得到5,10-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,7-bis(triisopropylsilyl)naphtho-[2,3-b:6,7-b']dithiophene
    参考文献:
    名称:
    Orthogonally Functionalized Naphthodithiophenes: Selective Protection and Borylation
    摘要:
    Selective functionalization protocols of naphtho[1,2-b;5,6-b']dithiophene (NDT3) by combining protection of the thiophene alpha-positions and direct borylation on the naphthalene core are described, which allows synthesizing a number of new NDT3-based building blocks with various substituents and isomeric NDT3-based polymers with different main chain structures. The same protocol is applicable to other isomeric naphthodithiophenes (NDTs), which affords a set of key building blocks for the development of elaborated functional pi-materials.
    DOI:
    10.1021/ol301797g
  • 作为产物:
    描述:
    三异丙基氯硅烷naphtho[2,3-b:6,7-b']dithiophene正丁基锂 作用下, 以 四氢呋喃正己烷 为溶剂, 反应 17.0h, 以97%的产率得到2,7-bis(triisopropylsilyl)naphtho[2,3-b:6,7-b']dithiophene
    参考文献:
    名称:
    Orthogonally Functionalized Naphthodithiophenes: Selective Protection and Borylation
    摘要:
    Selective functionalization protocols of naphtho[1,2-b;5,6-b']dithiophene (NDT3) by combining protection of the thiophene alpha-positions and direct borylation on the naphthalene core are described, which allows synthesizing a number of new NDT3-based building blocks with various substituents and isomeric NDT3-based polymers with different main chain structures. The same protocol is applicable to other isomeric naphthodithiophenes (NDTs), which affords a set of key building blocks for the development of elaborated functional pi-materials.
    DOI:
    10.1021/ol301797g
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