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1-(4-(2-bromoethoxy)phenyl)-2-phenyldiazene | 117346-13-1

中文名称
——
中文别名
——
英文名称
1-(4-(2-bromoethoxy)phenyl)-2-phenyldiazene
英文别名
(E)-[4-(2-bromoethoxy)phenyl](phenyl)diazene;[4-(2-bromoethoxy)phenyl]-phenyldiazene
1-(4-(2-bromoethoxy)phenyl)-2-phenyldiazene化学式
CAS
117346-13-1
化学式
C14H13BrN2O
mdl
——
分子量
305.174
InChiKey
ZTVXFNRCJJIOHK-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):
    4.8
  • 重原子数:
    18
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    34
  • 氢给体数:
    0
  • 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
  • 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:
    参考文献:
    名称:
    Preparation and optical characteristics of layered perovskite-type lead-bromide-incorporated azobenzene chromophores
    摘要:
    Lead bromide-based layered perovskite powders with azobenzene derivatives were prepared by a homogeneous precipitation method. From the diffuse reflectance (DR) and photoluminescence (PL) spectra of the hybrid powder materials, the present hybrids exhibited sharp absorption and PL peaks originating from excitons produced in the PbBr42- layer. When the present hybrid powder was irradiated with UV light at 350 nm, the absorption band from the trans-azobenzene chromophore, observed around 350 nm, decreased, while the absorption band from the cis-azobenzene chromophore, observed around 450 nm, increased. These results indicate that azobenzene chromophores in the present hybrid materials exhibit reversible photoisomerization. Moreover, it was found that the PL intensity from the exciton also varied due to photoisomerization of the azobenzene chromophores in the present hybrid. Thus, for the first time we succeeded in preparing the azobenzene derivative lead-bromide-based layered perovskite with photochromism before and after UV light irradiation. (c) 2012 Elsevier Inc. All rights reserved.
    DOI:
    10.1016/j.jssc.2012.11.009
  • 作为产物:
    描述:
    参考文献:
    名称:
    A dual thermal and photo-switchable shrinking–swelling supramolecular peptide dendron gel
    摘要:

    通过将一个以L-谷氨酸为端基的两亲性树状大分子与一个带正电的偶氮苯衍生物共同组装,制备了一种双重热和光可切换的收缩-膨胀超分子凝胶。

    DOI:
    10.1039/c5cc08076b
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文献信息

  • An azobenzene-modified redox-active ionic liquid electrolyte for supercapacitors
    作者:Yuhua Zhao、Yujuan Chen、Kelei Zhuo、Quanzhou Du、Dong Sun、Zhiyong Li、Huiyong Wang、Changling Yan、Jianji Wang
    DOI:10.1039/d2cc04081f
    日期:——
    A new redox-active ionic liquid (2-(4-(phenyldiazenyl)phenoxy)ethyl)-1-methyl-imidazolium tetrafluoroborate ([ABEMIM][BF4]) is demonstrated. It is incorporated into another ionic liquid ([EMIM][BF4]) to form a mixed IL electrolyte, which can markedly improve the capacitance performance of carbon-based supercapacitors via extra pseudocapacitance contribution. It opens up a new path to develop high-energy
    展示了一种新的具有氧化还原活性的离子液体(2-(4-(苯基二氮烯基)苯氧基)乙基)-1-甲基-咪唑鎓四氟硼酸盐([ABEMIM][BF 4 ])。将其掺入另一种离子液体([EMIM][BF 4 ])中形成混合IL电解质,可通过额外的赝电容贡献显着提高碳基超级电容器的电容性能。通过将氧化还原活性离子液体引入电解质,开辟了开发高能超级电容器的新途径。
  • A dual thermal and photo-switchable shrinking–swelling supramolecular peptide dendron gel
    作者:Fan Xie、Long Qin、Minghua Liu
    DOI:10.1039/c5cc08076b
    日期:——

    A dual thermal and photo-switchable shrinking–swelling supramolecular gel was fabricated through the co-assembly of an l-glutamic acid terminated amphiphilic dendron and a positively charged azobenzene derivative.

    通过将一个以L-谷氨酸为端基的两亲性树状大分子与一个带正电的偶氮苯衍生物共同组装,制备了一种双重热和光可切换的收缩-膨胀超分子凝胶。

  • Preparation and optical characteristics of layered perovskite-type lead-bromide-incorporated azobenzene chromophores
    作者:Ryo Sasai、Hisashi Shinomura
    DOI:10.1016/j.jssc.2012.11.009
    日期:2013.2
    Lead bromide-based layered perovskite powders with azobenzene derivatives were prepared by a homogeneous precipitation method. From the diffuse reflectance (DR) and photoluminescence (PL) spectra of the hybrid powder materials, the present hybrids exhibited sharp absorption and PL peaks originating from excitons produced in the PbBr42- layer. When the present hybrid powder was irradiated with UV light at 350 nm, the absorption band from the trans-azobenzene chromophore, observed around 350 nm, decreased, while the absorption band from the cis-azobenzene chromophore, observed around 450 nm, increased. These results indicate that azobenzene chromophores in the present hybrid materials exhibit reversible photoisomerization. Moreover, it was found that the PL intensity from the exciton also varied due to photoisomerization of the azobenzene chromophores in the present hybrid. Thus, for the first time we succeeded in preparing the azobenzene derivative lead-bromide-based layered perovskite with photochromism before and after UV light irradiation. (c) 2012 Elsevier Inc. All rights reserved.
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