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(19Z,110Z,79Z,710Z)-19,110,79,710-tetrahydro-2,6,8,12-tetraaza-1,7(9,10)-dianthracena-3,5,9,11(1,4)-tetrabenzenacyclododecaphane | 871682-38-1

中文名称
——
中文别名
——
英文名称
(19Z,110Z,79Z,710Z)-19,110,79,710-tetrahydro-2,6,8,12-tetraaza-1,7(9,10)-dianthracena-3,5,9,11(1,4)-tetrabenzenacyclododecaphane
英文别名
——
(19Z,110Z,79Z,710Z)-19,110,79,710-tetrahydro-2,6,8,12-tetraaza-1,7(9,10)-dianthracena-3,5,9,11(1,4)-tetrabenzenacyclododecaphane化学式
CAS
871682-38-1
化学式
C54H36N4
mdl
——
分子量
740.907
InChiKey
UKACHVFKQKVQBE-SJIZXIQESA-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):
    11.6
  • 重原子数:
    58.0
  • 可旋转键数:
    0.0
  • 环数:
    24.0
  • sp3杂化的碳原子比例:
    0.04
  • 拓扑面积:
    49.44
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

反应信息

  • 作为反应物:
    描述:
    (19Z,110Z,79Z,710Z)-19,110,79,710-tetrahydro-2,6,8,12-tetraaza-1,7(9,10)-dianthracena-3,5,9,11(1,4)-tetrabenzenacyclododecaphanetin三氟乙酸 作用下, 以 乙腈 为溶剂, 反应 12.0h, 以100%的产率得到2,12,21,31-Tetrazaundecacyclo[30.6.6.613,20.23,6.28,11.222,25.227,30.014,19.033,38.039,44.049,54]octapentaconta-1(39),3(58),4,6(57),8(56),9,11(55),13,15,17,19,22,24,27,29,32(44),33,35,37,40,42,45,47,49,51,53-hexacosaene
    参考文献:
    名称:
    An Electric Cyclophane:  Cavity Control Based on the Rotation of a Paraphenylene by Redox Switching
    摘要:
    Although a free rotation around a single bond gives no mechanical output, it has let us imagine a molecular motor. A para-substituted aromatic ring can be regarded as a rotator with the para-rotation axis. When it is incorporated in a wider pi-conjugated system, a quinoidal structure is generated accompanied by oxidation on the substituted groups at the 1,4-position, and the axis is fixed. A paraphenylenediamine was selected as the nanomechanical molecular module capable of locking and releasing the free rotation using an electrode in solution. We inserted the module into a simple molecular system, cyclophane. It was clarified that the cyclophane was able to open and close its cavity in a reversible redox process repeatedly.
    DOI:
    10.1021/ja055681i
  • 作为产物:
    描述:
    蒽醌4,4'-二氨基二苯甲烷三乙烯二胺四氯化钛 作用下, 以 氯苯 为溶剂, 反应 16.0h, 以16%的产率得到
    参考文献:
    名称:
    An Electric Cyclophane:  Cavity Control Based on the Rotation of a Paraphenylene by Redox Switching
    摘要:
    Although a free rotation around a single bond gives no mechanical output, it has let us imagine a molecular motor. A para-substituted aromatic ring can be regarded as a rotator with the para-rotation axis. When it is incorporated in a wider pi-conjugated system, a quinoidal structure is generated accompanied by oxidation on the substituted groups at the 1,4-position, and the axis is fixed. A paraphenylenediamine was selected as the nanomechanical molecular module capable of locking and releasing the free rotation using an electrode in solution. We inserted the module into a simple molecular system, cyclophane. It was clarified that the cyclophane was able to open and close its cavity in a reversible redox process repeatedly.
    DOI:
    10.1021/ja055681i
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