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2,2'-(5,5'-(9,9-didecyl-9H-fluorene-2,7-diyl)bis-(ethyne-2,1-diyl)bis(thiophene-5,2-diyl))dibenzothiazole | 1225449-67-1

中文名称
——
中文别名
——
英文名称
2,2'-(5,5'-(9,9-didecyl-9H-fluorene-2,7-diyl)bis-(ethyne-2,1-diyl)bis(thiophene-5,2-diyl))dibenzothiazole
英文别名
2,2'-(5,5'-(9,9'-didecyl-9H-fluorene-2,7-diyl)bis(ethyne-2,1-diyl)-(thiophen-5,2-diyl))dibenzothiazole;2-[5-[2-[7-[2-[5-(1,3-Benzothiazol-2-yl)thiophen-2-yl]ethynyl]-9,9-didecylfluoren-2-yl]ethynyl]thiophen-2-yl]-1,3-benzothiazole
2,2'-(5,5'-(9,9-didecyl-9H-fluorene-2,7-diyl)bis-(ethyne-2,1-diyl)bis(thiophene-5,2-diyl))dibenzothiazole化学式
CAS
1225449-67-1
化学式
C59H60N2S4
mdl
——
分子量
925.403
InChiKey
YWCKMTSWQYFXEG-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):
    22
  • 重原子数:
    65
  • 可旋转键数:
    24
  • 环数:
    9.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    139
  • 氢给体数:
    0
  • 氢受体数:
    6

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-(5-bromothiophen-2-yl)benzo[d]thiazole 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodide三乙胺 、 potassium hydroxide 作用下, 以 甲苯 为溶剂, 反应 9.03h, 生成 2,2'-(5,5'-(9,9-didecyl-9H-fluorene-2,7-diyl)bis-(ethyne-2,1-diyl)bis(thiophene-5,2-diyl))dibenzothiazole
    参考文献:
    名称:
    Two-Photon Fluorescence Lysosomal Bioimaging with a Micelle-Encapsulated Fluorescent Probe
    摘要:
    我们报告了一种新型、高效、溶酶体选择性系统的双光子荧光显微镜(2PFM)成像和体外细胞存活率,该系统基于封装在 Pluronic® F-127 胶束中的双光子吸收(2PA)荧光探针(I)。染料 I 的制备是通过微波辅助合成完成的,从而提高了产量并缩短了反应时间。光物理特性分析表明,该探针具有显著的 2PA 效率。
    DOI:
    10.1007/s10895-010-0801-3
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文献信息

  • A Series of Fluorene-Based Two-Photon Absorbing Molecules: Synthesis, Linear and Nonlinear Characterization, and Bioimaging
    作者:Carolina D. Andrade、Ciceron O. Yanez、Luis Rodriguez、Kevin D. Belfield
    DOI:10.1021/jo1005075
    日期:2010.6.18
    The synthesis, structural, and photophysical characterization of a series of new fluorescent donor acceptor and acceptor-acceptor molecules, based on the fluorenyl ring system, with two-photon absorbing properties is described. These new compounds exhibited large Stokes shifts, high fluorescence quantum yields, and significantly, high two-photon absorption cross sections, making them well suited for two-photon fluorescence microscopy imaging. Confocal and two-photon fluorescence microscopy imaging of COS-7 and HCT 116 cells incubated with probe I showed endosomal selectivity, demonstrating the potential of this class of fluorescent probes in multiphoton fluorescence microscopy.
  • New Two-Photon-Absorbing Probe with Efficient Superfluorescent Properties
    作者:Kevin D. Belfield、Carolina D. Andrade、Ciceron O. Yanez、Mykhailo V. Bondar、Florencio E. Hernandez、Olga V. Przhonska
    DOI:10.1021/jp107343k
    日期:2010.11.11
    The synthesis, linear photophysical, and photochemical parameters, two-photon absorption (2PA), and superfluorescence properties of 2,2'-(5,5'-(9,9-didecyl-9H-fluorene-2,7-diyl)bis(ethyne-2,1-diyl)bis(thiophene-5,2-diy1))dibenzo[d]thiazole (1) were investigated, suggesting its potential as an efficient fluorescent probe for bioimaging applications. The steady-state absorption, fluorescence, and excitation anisotropy spectra of 1 were measured in several organic solvents and aqueous media. Probe 1 exhibited high fluorescence quantum yield (similar to 0.7-0.8) and photochemical stability (photobleaching quantum yield similar to(3-7) x 10(-6)). The 2PA spectra were determined over a broad spectral range (640-920 nm) using a standard two-photon induced fluorescence method under femtosecond excitation. A well-defined two-photon allowed absorption band at 680-720 nm with corresponding 2PA cross sections delta(2PA) approximate to 800-900 GM was observed. The use of probe 1 in bioimaging was shown via one- and two-photon fluorescence imaging of HCT-116 cells. An amplification of the stimulated emission of 1 was demonstrated in organic solvents and thin polystyrene films, which potentially can be used for the development of new fluorescent labels with increased spectral brightness.
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