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2,4-dichlorophenyl vinyl sulfide | 1447737-61-2

中文名称
——
中文别名
——
英文名称
2,4-dichlorophenyl vinyl sulfide
英文别名
2,4-Dichloro-1-ethenylsulfanylbenzene
2,4-dichlorophenyl vinyl sulfide化学式
CAS
1447737-61-2
化学式
C8H6Cl2S
mdl
——
分子量
205.108
InChiKey
FSVWNTZQRMZIIC-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):
    4.2
  • 重原子数:
    11
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    25.3
  • 氢给体数:
    0
  • 氢受体数:
    1

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:
    2,4-二氯苯硫酚1,2-二溴乙烷sodium ethanolate 作用下, 以 乙醇 为溶剂, 反应 10.5h, 以50%的产率得到2,4-dichlorophenyl vinyl sulfide
    参考文献:
    名称:
    RAFT Polymerization of S-Vinyl Sulfide Derivatives and Synthesis of Block Copolymers Having Two Distinct Optoelectronic Functionalities
    摘要:
    Well-defined sulfur-containing polymers and block copolymers were synthesized by reversible addition-fragmentation chain transfer (RAFT) polymerization of S-vinyl sulfide derivatives, in which the thioether moiety is directly connected to the vinyl group. We initially investigated RAFT polymerization of four different S-vinyl sulfide derivatives, phenyl vinyl sulfide (PVS), 4-chlorophenyl vinyl sulfide (CPVS), 2,4-dichlorophenyl vinyl sulfide (DCPVS), and 4-bromophenyl vinyl sulfide (BPVS). Three xanthate-type chain transfer agents (CTAs), a dithiocarbamate-type CTA, and a dithioester-type CTA were compared for these RAFT polymerizations. Reasonable control of the polymerization of PVS was confirmed by an observed linear increase in the molecular weight with the conversion, feasibility to control molecular weight based on the ratio of monomer consumed to the amount of CTA used, chain end structure determined by H-1 NMR, and chain extension experiment. The RAFT polymerization of the bromo-substituted monomer (BPVS) also proceeded in the controlled fashion under the same conditions. Incorporation of optoelectronic groups, including anthracene, fluorene, diphenylamine, and phenothiazine on the bromophenyl pendant group of poly(BPVS) were accomplished by palladium-catalyzed postmodifications. We also investigated characteristic optoelectronic properties of modified polymers and block copolymers with two distinct electronic functionalities.
    DOI:
    10.1021/ma400813e
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