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3-[1,3-bis(carbazol-9-yl)propan-2-oxymethyl]-3-methyloxetane | 1352171-06-2

中文名称
——
中文别名
——
英文名称
3-[1,3-bis(carbazol-9-yl)propan-2-oxymethyl]-3-methyloxetane
英文别名
9-[3-Carbazol-9-yl-2-[(3-methyloxetan-3-yl)methoxy]propyl]carbazole;9-[3-carbazol-9-yl-2-[(3-methyloxetan-3-yl)methoxy]propyl]carbazole
3-[1,3-bis(carbazol-9-yl)propan-2-oxymethyl]-3-methyloxetane化学式
CAS
1352171-06-2
化学式
C32H30N2O2
mdl
——
分子量
474.602
InChiKey
DSUGXCZIABFIEA-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):
    6.5
  • 重原子数:
    36
  • 可旋转键数:
    7
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    28.3
  • 氢给体数:
    0
  • 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

反应信息

  • 作为产物:
    描述:
    9-(环氧-2-甲基)-9H-咔唑苄基三甲基氯化铵 、 sodium hydride 、 potassium hydroxide 作用下, 以 丁酮 为溶剂, 反应 120.0h, 生成 3-[1,3-bis(carbazol-9-yl)propan-2-oxymethyl]-3-methyloxetane
    参考文献:
    名称:
    Glass-forming 1,3-bis(carbazol-9-yl)propan-2-ol based monomers and polymers
    摘要:
    Three glass-forming 1,3-bis(carbazol-9-yl)propan-2-ol based monomers, i.e. oxirane, thiirane and oxetane were synthesized. Photopolymerization of their solid amorphous layers initiated with diphenyliodonium tetrafluoroborate and the dark polymerization in solutions initiated with boron trifluoride etherate were performed. The number-average molecular weights of the obtained polymers are in the range of 1000-19,400. The highest initial polymerization rate, the highest limit conversion and the highest molecular weight were observed for the polymerization of thiirane. Optical, photophysical, electrochemical and thermal properties of the synthesized compounds were studied. UV and fluorescence spectra of the compounds have the similar profiles, due to the presence of the same chromophore. No excimer emission was observed neither for dilute solutions of monomers nor polymers. The electrochemical coupling was observed for all the synthesized 1,3-bis(carbazol-9-yl)propan-2-ol based monomers and polymers by cyclic voltammetry. The thermal degradation of the derivatives of 1,3-bis(carbazol-9-yl)propan-2-ol derivatives starts in the range of the temperatures from 317 to 402. The glass transition temperatures of the monomers range from 43 to 58 while glass transition temperatures of the polymers are in the range of 103-125. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.reactfunctpolym.2011.08.010
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文献信息

  • Glass-forming 1,3-bis(carbazol-9-yl)propan-2-ol based monomers and polymers
    作者:Egle Andrikaityte、Monika Cekaviciute、Jurate Simokaitiene、Gintaras Buika、Juozas Vidas Grazulevicius、Vitalija Rubeziene
    DOI:10.1016/j.reactfunctpolym.2011.08.010
    日期:2012.1
    Three glass-forming 1,3-bis(carbazol-9-yl)propan-2-ol based monomers, i.e. oxirane, thiirane and oxetane were synthesized. Photopolymerization of their solid amorphous layers initiated with diphenyliodonium tetrafluoroborate and the dark polymerization in solutions initiated with boron trifluoride etherate were performed. The number-average molecular weights of the obtained polymers are in the range of 1000-19,400. The highest initial polymerization rate, the highest limit conversion and the highest molecular weight were observed for the polymerization of thiirane. Optical, photophysical, electrochemical and thermal properties of the synthesized compounds were studied. UV and fluorescence spectra of the compounds have the similar profiles, due to the presence of the same chromophore. No excimer emission was observed neither for dilute solutions of monomers nor polymers. The electrochemical coupling was observed for all the synthesized 1,3-bis(carbazol-9-yl)propan-2-ol based monomers and polymers by cyclic voltammetry. The thermal degradation of the derivatives of 1,3-bis(carbazol-9-yl)propan-2-ol derivatives starts in the range of the temperatures from 317 to 402. The glass transition temperatures of the monomers range from 43 to 58 while glass transition temperatures of the polymers are in the range of 103-125. (C) 2011 Elsevier Ltd. All rights reserved.
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