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6-(N-methyl-N-phenylamino)hexyl methacrylate | 155296-41-6

中文名称
——
中文别名
——
英文名称
6-(N-methyl-N-phenylamino)hexyl methacrylate
英文别名
6-(N-methylanilino)hexyl 2-methylprop-2-enoate
6-(N-methyl-N-phenylamino)hexyl methacrylate化学式
CAS
155296-41-6
化学式
C17H25NO2
mdl
——
分子量
275.391
InChiKey
FWRIOIAKLLDKHL-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):
    4.3
  • 重原子数:
    20
  • 可旋转键数:
    10
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.47
  • 拓扑面积:
    29.5
  • 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:
    Photoresponsive behavior of two well-defined azo polymers with different electron-withdrawing groups on push–pull azo chromophores
    摘要:
    Two well-defined methacrylate-based azo polymers bearing strong push pull azo chromophores were synthesized by RAFT polymerization. The polymers contain cyano and carboxyl as electron-withdrawing groups at 4-positions of the azo chromophores. The polymers exhibited significantly different photo-responsive properties on all light-driven motion levels. When irradiated with a linearly polarized laser beam at 532 nm, the cyanoazobenzene-containing polymer showed rapid birefringence growth relative to that of the carboxylazobenzene-containing polymer. When the light was switched off, a much lower orientation decay was observed for the carboxylazobenzene-containing polymer compared with its counterpart. Upon irradiation with the interfering laser beams at these two wavelengths, surface-relief-grating amplitude formed on the film of the cyanoazobenzene-containing polymer and was substantially larger than that for the carboxyl substituted polymer. When the polymer films were irradiated with a homogenous laser beam at 488 and 532 nm, self-structured surface pattern. was only detected for the cyanoazobenzene-containing polymer with the 532 nm light irradiation. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.dyepig.2013.05.006
  • 作为产物:
    参考文献:
    名称:
    带有强推挽式偶氮发色团和胆固醇基的光敏二嵌段共聚物
    摘要:
    通过可逆加成断裂链转移(RAFT)聚合反应,合成了一系列在各自嵌段上带有强推挽式偶氮发色团和胆固醇基团的二嵌段共聚物。通过DSC,POM,AFM,XRD和激光辐照研究了嵌段共聚物的液晶相结构,微相分离形态和光响应性能。结果表明,胆固醇基嵌段(PChEMA)形成近晶A中间相,其形态取决于偶氮嵌段(PAzoCN)的长度。当偶氮嵌段较短时,例如PChEMA 50 - b -PAzoCN 7,则无法鉴定出微相分离。对于PChEMA 50 - b -PAzoCN 28,PAzoCN表现为嵌入PChEMA基质中的六方堆积纳米圆柱。当偶氮嵌段长度进一步增加时,嵌段共聚物PChEMA 50 - b - PAzoCN 73形成微相分离的薄片。微相分离对偶氮发色团的光致取向没有明显的限制,但是相限制限制了光响应性PAzoCN嵌段的微米级质量传输。
    DOI:
    10.1016/j.polymer.2012.05.063
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文献信息

  • Photoresponsive diblock copolymers bearing strong push–pull azo chromophores and cholesteryl groups
    作者:Yu Zhu、Yuqi Zhou、Zhen Chen、Ran Lin、Xiaogong Wang
    DOI:10.1016/j.polymer.2012.05.063
    日期:2012.7
    (PChEMA) forms smectic-A mesophase and the morphology depends on the length of the azo block (PAzoCN). When the azo block is short, such as PChEMA50-b-PAzoCN7, no microphase separation can be identified. For PChEMA50-b-PAzoCN28, PAzoCN appears as the hexagonal-packed nanocylinders embedded in the PChEMA matrix. When the azo block length further increases, the block copolymer PChEMA50-b-PAzoCN73 forms microphase-separated
    通过可逆加成断裂链转移(RAFT)聚合反应,合成了一系列在各自嵌段上带有强推挽式偶氮发色团和胆固醇基团的二嵌段共聚物。通过DSC,POM,AFM,XRD和激光辐照研究了嵌段共聚物的液晶相结构,微相分离形态和光响应性能。结果表明,胆固醇基嵌段(PChEMA)形成近晶A中间相,其形态取决于偶氮嵌段(PAzoCN)的长度。当偶氮嵌段较短时,例如PChEMA 50 - b -PAzoCN 7,则无法鉴定出微相分离。对于PChEMA 50 - b -PAzoCN 28,PAzoCN表现为嵌入PChEMA基质中的六方堆积纳米圆柱。当偶氮嵌段长度进一步增加时,嵌段共聚物PChEMA 50 - b - PAzoCN 73形成微相分离的薄片。微相分离对偶氮发色团的光致取向没有明显的限制,但是相限制限制了光响应性PAzoCN嵌段的微米级质量传输。
  • JPH11322690A
    申请人:——
    公开号:JPH11322690A
    公开(公告)日:1999-11-24
  • Photoresponsive behavior of two well-defined azo polymers with different electron-withdrawing groups on push–pull azo chromophores
    作者:Yu Zhu、Yuqi Zhou、Xiaogong Wang
    DOI:10.1016/j.dyepig.2013.05.006
    日期:2013.10
    Two well-defined methacrylate-based azo polymers bearing strong push pull azo chromophores were synthesized by RAFT polymerization. The polymers contain cyano and carboxyl as electron-withdrawing groups at 4-positions of the azo chromophores. The polymers exhibited significantly different photo-responsive properties on all light-driven motion levels. When irradiated with a linearly polarized laser beam at 532 nm, the cyanoazobenzene-containing polymer showed rapid birefringence growth relative to that of the carboxylazobenzene-containing polymer. When the light was switched off, a much lower orientation decay was observed for the carboxylazobenzene-containing polymer compared with its counterpart. Upon irradiation with the interfering laser beams at these two wavelengths, surface-relief-grating amplitude formed on the film of the cyanoazobenzene-containing polymer and was substantially larger than that for the carboxyl substituted polymer. When the polymer films were irradiated with a homogenous laser beam at 488 and 532 nm, self-structured surface pattern. was only detected for the cyanoazobenzene-containing polymer with the 532 nm light irradiation. (C) 2013 Elsevier Ltd. All rights reserved.
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