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4-dodecyloxy-3,5-bis(2-trimethylsilylphenyliminomethyl)phenylacetylene | 1427772-65-3

中文名称
——
中文别名
——
英文名称
4-dodecyloxy-3,5-bis(2-trimethylsilylphenyliminomethyl)phenylacetylene
英文别名
1-[2-dodecoxy-5-ethynyl-3-[(2-trimethylsilylphenyl)iminomethyl]phenyl]-N-(2-trimethylsilylphenyl)methanimine
4-dodecyloxy-3,5-bis(2-trimethylsilylphenyliminomethyl)phenylacetylene化学式
CAS
1427772-65-3
化学式
C40H56N2OSi2
mdl
——
分子量
637.068
InChiKey
VZQAGCXLUVNAEK-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):
    10.56
  • 重原子数:
    45
  • 可旋转键数:
    19
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    34
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    参考文献:
    名称:
    Living-like helix-sense-selective polymerization of an achiral substituted acetylene having bulky substituents
    摘要:
    By using a new achiral phenylacetylene having bulky substituents as a monomer, living-like helix-sense-selective polymerization (HSSP) has been achieved. This is the first example of the HSSP of substituted acetylenes where the degree of polymerization was controlled. The resulting one-handed helical living polymer initiated polymerization of a second monomer to successfully yield a block copolymer. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.polymer.2013.02.009
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文献信息

  • Living-like helix-sense-selective polymerization of an achiral substituted acetylene having bulky substituents
    作者:Yu Zang、Kazuki Nakao、Hiroki Yotsuyanagi、Toshiki Aoki、Takeshi Namikoshi、Toyokazu Tsutsuba、Masahiro Teraguchi、Takashi Kaneko
    DOI:10.1016/j.polymer.2013.02.009
    日期:2013.3
    By using a new achiral phenylacetylene having bulky substituents as a monomer, living-like helix-sense-selective polymerization (HSSP) has been achieved. This is the first example of the HSSP of substituted acetylenes where the degree of polymerization was controlled. The resulting one-handed helical living polymer initiated polymerization of a second monomer to successfully yield a block copolymer. (C) 2013 Elsevier Ltd. All rights reserved.
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