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rac-3,3'-diiodbimesityl | 37055-18-8

中文名称
——
中文别名
——
英文名称
rac-3,3'-diiodbimesityl
英文别名
3,3'-Diiodbimesityl;3,3'-Dijod-bimesityl;3,3'-diiodobimesityl;2-Iodo-4-(3-iodo-2,4,6-trimethylphenyl)-1,3,5-trimethylbenzene
rac-3,3'-diiodbimesityl化学式
CAS
37055-18-8;37055-20-2
化学式
C18H20I2
mdl
——
分子量
490.166
InChiKey
ZDLUNNZGOMIINK-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):
    7
  • 重原子数:
    20
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

上下游信息

  • 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:
    描述:
    rac-3,3'-diiodbimesitylN-溴代丁二酰亚胺(NBS)三氟乙酸 作用下, 以 乙腈 为溶剂, 以90 %的产率得到
    参考文献:
    名称:
    一种六甲基联苯衍生物及其制备方法和应用
    摘要:
    本发明属于有机光电材料技术领域,具体涉及一种六甲基联苯衍生物及其制备方法应用,所述衍生物其具有式(1)所示的结构:X1、X2、X3、X4相同或不同、彼此独立地选自单键、碳原子、硅原子、氧原子、硫原子、氮原子、磷原子、硼原子、羰基(‑C=O‑)、砜基(‑SO2‑)、亚砜基(‑S=O‑)、膦氧基(‑P=O‑)、C6~18的芳基或者C5‑18的杂芳基。本发明六甲基联苯衍生物具有良好的热稳定性、成膜性能以及较高的发光效率,可用于制备有机电致发光器件、有机太阳能电池和有机场效应晶体管等电子器件。
    公开号:
    CN115716797A
  • 作为产物:
    描述:
    bimesitylN-碘代丁二酰亚胺三氟乙酸 作用下, 以 乙腈 为溶剂, 以92 %的产率得到rac-3,3'-diiodbimesityl
    参考文献:
    名称:
    一种六甲基联苯衍生物及其制备方法和应用
    摘要:
    本发明属于有机光电材料技术领域,具体涉及一种六甲基联苯衍生物及其制备方法应用,所述衍生物其具有式(1)所示的结构:X1、X2、X3、X4相同或不同、彼此独立地选自单键、碳原子、硅原子、氧原子、硫原子、氮原子、磷原子、硼原子、羰基(‑C=O‑)、砜基(‑SO2‑)、亚砜基(‑S=O‑)、膦氧基(‑P=O‑)、C6~18的芳基或者C5‑18的杂芳基。本发明六甲基联苯衍生物具有良好的热稳定性、成膜性能以及较高的发光效率,可用于制备有机电致发光器件、有机太阳能电池和有机场效应晶体管等电子器件。
    公开号:
    CN115716797A
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文献信息

  • IBX−I<sub>2</sub>Redox Couple for Facile Generation of IOH and I<sup>+</sup>: Expedient Protocol for Iodohydroxylation of Olefins and Iodination of Aromatics
    作者:Jarugu Narasimha Moorthy、Kalyan Senapati、Sarvesh Kumar
    DOI:10.1021/jo9007892
    日期:2009.8.21
    IBX is readily reduced to IBA in the presence of molecular iodine in DMSO to generate hypoiodous acid (IOH). which reacts with a variety of olefins as well as alpha, beta-unsaturated ketones leading to their respective iodohydrins with anti stereochemistry. The same redox chemistry in acetonitrile containing TFA produces iodonium lolls for facile Iodination of a variety of aromatic compounds in respectable isolated yields.
  • Bloch,M. et al., Chemische Berichte, 1972, vol. 105, p. 1790 - 1797
    作者:Bloch,M. et al.
    DOI:——
    日期:——
  • De Novo Design for Functional Amorphous Materials: Synthesis and Thermal and Light-Emitting Properties of<i>Twisted</i>Anthracene-Functionalized Bimesitylenes
    作者:Jarugu Narasimha Moorthy、Parthasarathy Venkatakrishnan、Palani Natarajan、Duo-Fong Huang、Tahsin J. Chow
    DOI:10.1021/ja8042905
    日期:2008.12.24
    The unique structural attributes inherent to D-2d-symmetric rigid tetraarylbimesityls render their close packing in the solid state difficult. We have exploited the indisposed tendency of such modules based on the bimesityl scaffold toward crystallization to design a novel class of amorphous functional materials with high glass transition temperatures and thermal stability (T-d > 400 degrees C). It is shown that a variety of 2- and 4-fold anthracene-functionalized bimesityls, 1-7, that exhibit excellent amorphous properties (T-g = ca. 190-330 degrees C) can be readily prepared via facile Pd(0)-mediated cross-coupling strategies. As the communication between the bimesityl core and the anchored anthracenes is negligible or only marginal, the trends observed for luminescence of model constituent anthracenes are reproduced in the condensed-phase photoluminescence and electroluminescence of 1-7. In other words, the emission characteristics, i.e., lambda(max) and quantum yields, are readily modulated via appropriate modification of the fluorophores. The functional behavior of this unique class of amorphous materials based on the bimesityl scaffold is demonstrated by fabrication of OLED devices. The 2-fold functionalized derivatives 1 and 2 lend themselves to sublimation techniques, so that the electroluminescence is captured with high efficiencies at low turn-on voltages (3.5-6.5 V). The device ITO/NPB (400 angstrom)/1 % 2:MADN (400 angstrom)/TPBI (400 angstrom)/LiF (10 angstrom)/Al (1500 angstrom) for 2 yields the, highest luminance of similar to 13 900 cd/m(2) at 17.5 V, a maximum luminance efficiency of similar to 7.4 cd/A at 4.5 V, and a power efficiency of similar to 5.3 lm/W at 4.0 V. Further, at a brightness of 800 cd/m(2) and a current density of 13.8 mA/cm(2), the device is found to exhibit excellent luminance efficiency of 5.8 cd/A, external quantum efficiency of 4.3% with a power efficiency of 2.2 Im/W, and pure blue light with a CIEx,y (x = 0.13, y = 0.18). The performance characteristics of the devices fabricated for 1 and 2 are remarkable. Although the 4-fold functionalized systems did not permit sublimation leading to spin-coating as a means for device fabrication, the observed electroluminescence for 4 and 5 attests to a broader scope and applicability of this new category of amorphous molecules for application in OLEDs.
  • Nondoped Pure-Blue OLEDs Based on Amorphous Phenylenevinylene-Functionalized Twisted Bimesitylenes
    作者:Jarugu Narasimha Moorthy、Parthasarathy Venkatakrishnan、Palani Natarajan、Zhenghuan Lin、Tahsin J. Chow
    DOI:10.1021/jo1001565
    日期:2010.4.16
    The twisted bimesitylene scaffold hinders crystallization and imparts amorphous nature to the oligophenylenevinylenes (OPVs) generated by 2- and/or 4-fold functionalization. The resultant phenylenevinylenes 1-5 with unique molecular topology exhibit excellent thermal and solid-state luminescence properties. The amorphous nature permits their application as pure-blue emissive materials in OLEDs. Under nondoped conditions, the device performances observed surpass those for analogous and simple oligophenylenevinylenes known so far; for example, the device based on OPV 2 as an emitting material and structurally analogous Bim-DPAB as a hole-transporting material yields pure-blue electroluminescence with an external quantum efficiency of ca. 4.70% at 20 mA/cm(2), which is higher than those reported for nondoped pure-blue OPV emitters.
  • Fischer, Erika; Hess, Heinrich; Lorenz, Thomas, Chemische Berichte, 1991, vol. 124, # 4, p. 783 - 789
    作者:Fischer, Erika、Hess, Heinrich、Lorenz, Thomas、Musso, Hans、Rossnagel, Ingrid
    DOI:——
    日期:——
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