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11,22-Bis(2,5-dithiophen-2-ylthiophen-3-yl)-7,18-dioctyl-7,18-diazaheptacyclo[14.6.2.22,5.03,12.04,9.013,23.020,24]hexacosa-1(22),2,4,9,11,13(23),14,16(24),20,25-decaene-6,8,17,19-tetrone | 1227479-88-0

中文名称
——
中文别名
——
英文名称
11,22-Bis(2,5-dithiophen-2-ylthiophen-3-yl)-7,18-dioctyl-7,18-diazaheptacyclo[14.6.2.22,5.03,12.04,9.013,23.020,24]hexacosa-1(22),2,4,9,11,13(23),14,16(24),20,25-decaene-6,8,17,19-tetrone
英文别名
11,22-bis(2,5-dithiophen-2-ylthiophen-3-yl)-7,18-dioctyl-7,18-diazaheptacyclo[14.6.2.22,5.03,12.04,9.013,23.020,24]hexacosa-1(22),2,4,9,11,13(23),14,16(24),20,25-decaene-6,8,17,19-tetrone
11,22-Bis(2,5-dithiophen-2-ylthiophen-3-yl)-7,18-dioctyl-7,18-diazaheptacyclo[14.6.2.22,5.03,12.04,9.013,23.020,24]hexacosa-1(22),2,4,9,11,13(23),14,16(24),20,25-decaene-6,8,17,19-tetrone化学式
CAS
1227479-88-0
化学式
C64H54N2O4S6
mdl
——
分子量
1107.54
InChiKey
VPGCIJMAHMRZLR-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):
    18.7
  • 重原子数:
    76
  • 可旋转键数:
    20
  • 环数:
    13.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    244
  • 氢给体数:
    0
  • 氢受体数:
    10

反应信息

  • 作为产物:
    描述:
    四丁基氟化铵 作用下, 以 四氢呋喃 为溶剂, 以78%的产率得到11,22-Bis(2,5-dithiophen-2-ylthiophen-3-yl)-7,18-dioctyl-7,18-diazaheptacyclo[14.6.2.22,5.03,12.04,9.013,23.020,24]hexacosa-1(22),2,4,9,11,13(23),14,16(24),20,25-decaene-6,8,17,19-tetrone
    参考文献:
    名称:
    Terthiophene−Perylene diimides: Color Tuning via Architecture Variation
    摘要:
    N,N'-Bisoctylperylene diimides (PDIs) have been functionalized in the 1,7-position with terthiophenes of varying architecture giving three new donor-acceptor (D-A) compounds of the same molecular weight Different conjugation lengths, arrangements, and connections of the thiophene units within themselves and toward the PDI core have strong effects on the optical, electronic, and photochemical properties of the D-A compounds Like jigsaw pieces joined together to give different pictures, the terthiophenes are linked to PDIs to achieve different colors These insights into tuning color and energy levels can open new possibilities for tailoring chromophores to their desired applications, e g, organic photovoltaics or organic field effect transistors
    DOI:
    10.1021/jp911800q
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文献信息

  • Terthiophene−Perylene diimides: Color Tuning via Architecture Variation
    作者:Henrike Wonneberger、Chang-Qi Ma、Martina A. Gatys、Chen Li、Peter Bäuerle、Klaus Müllen
    DOI:10.1021/jp911800q
    日期:2010.11.18
    N,N'-Bisoctylperylene diimides (PDIs) have been functionalized in the 1,7-position with terthiophenes of varying architecture giving three new donor-acceptor (D-A) compounds of the same molecular weight Different conjugation lengths, arrangements, and connections of the thiophene units within themselves and toward the PDI core have strong effects on the optical, electronic, and photochemical properties of the D-A compounds Like jigsaw pieces joined together to give different pictures, the terthiophenes are linked to PDIs to achieve different colors These insights into tuning color and energy levels can open new possibilities for tailoring chromophores to their desired applications, e g, organic photovoltaics or organic field effect transistors
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