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1H,1'H-2,2'-biphenyl-4,4'-diyl-bis-benzoimidazole | 15339-68-1

中文名称
——
中文别名
——
英文名称
1H,1'H-2,2'-biphenyl-4,4'-diyl-bis-benzoimidazole
英文别名
4,4'-Bis-benzimidazol-2-yl-biphenyl;4,4'-Di-(2-benzimidazolyl)biphenyl;Bisbenzimidazolyl biphenyl;2-[4-[4-(1H-benzimidazol-2-yl)phenyl]phenyl]-1H-benzimidazole
1<i>H</i>,1'<i>H</i>-2,2'-biphenyl-4,4'-diyl-bis-benzoimidazole化学式
CAS
15339-68-1
化学式
C26H18N4
mdl
——
分子量
386.456
InChiKey
PQJBJKXEXHGYPG-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

物化性质

  • 熔点:
    495 °C
  • 沸点:
    680.3±65.0 °C(Predicted)
  • 密度:
    1.302±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6.1
  • 重原子数:
    30
  • 可旋转键数:
    3
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    57.4
  • 氢给体数:
    2
  • 氢受体数:
    2

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

  • 作为反应物:
    参考文献:
    名称:
    调节共轭刚性平面结构以实现荧光识别特性的转变
    摘要:
    双苯并咪唑是一类重要的荧光分子探针材料,在环境、临床和生物系统中都有应用。此外,不同的双苯并咪唑衍生物由于具有优异的配位特性和荧光特性,被广泛研究用于阳离子识别。在本研究中,探讨了三种双苯并咪唑衍生物(B 1、B 2和B 3)与苯基共轭体系的增加和用于检测有毒重金属离子(如 Hg 2+ )的荧光传感特性之间的关系。并进行了分析。B 1包含一个没有附加物的双苯并咪唑单元,而B 2和B 3在两个苯并咪唑环之间具有不同的苯基附属物;随着共轭体系的扩展,阳离子识别的选择性增加,但稳定性显着降低。同时,通过荧光光谱、1 H NMR光谱、ICP分析和DFT计算等方法研究了它们对Hg 2+的检测限(LOD)和识别机制。令人鼓舞的是,B 2表现出较高的吸附和分离效率,为汞离子吸附/去除材料的开发提供了参考。
    DOI:
    10.1039/d1nj05911d
  • 作为产物:
    参考文献:
    名称:
    KORSHAK V. V.; GVERDTSITELI I. M.; KIPIANI L. G.; TABIDZE R. S.; LEKAS T.+, IZV. AN GRUZSSR. CEP. XIM., 1979, 5, HO 3, 210-216
    摘要:
    DOI:
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文献信息

  • Rigid-rod benzimidazole pendant benzobisazo polymer
    申请人:The United States of America as represented by the Secretary of the Air
    公开号:US05140092A1
    公开(公告)日:1992-08-18
    Provided is a para-ordered aromatic heterocyclic polymer having repeating units of the formula --(--Q--Ar--)-- wherein Q is ##STR1## wherein X is --O--, --NH-- or --S--, and wherein Ar is ##STR2##
    提供的是一个带有芳香杂环的聚合物,其重复单元的公式为--(--Q--Ar--)--,其中Q为##STR1##,其中X为--O--,--NH--或--S--,而Ar为##STR2##。
  • Microwave-assisted Synthesis of Aryl and Heteroaryl Derivatives of Benzimidazole
    作者:Hideko Koshima、Haitao Yu、Hirohisa Kawanishi
    DOI:10.3987/com-03-9760
    日期:——
  • PARTICLE-DISPERSED POLYIMIDE PRECURSOR SOLUTION, METHOD FOR PRODUCING POROUS POLYIMIDE FILM, AND POROUS POLYIMIDE FILM
    申请人:FUJIFILM Business Innovation Corp.
    公开号:US20220119596A1
    公开(公告)日:2022-04-21
    A particle-dispersed polyimide precursor solution contains a polyimide precursor having a unit represented by the following formula (I), particles, and a solvent, in which the particle-dispersed polyimide precursor solution satisfies both the following conditions (1) and (2), (in the formula (I), A represents a tetravalent organic group, and B represents a divalent organic group represented by any of the following formulas (B1) to (B4)), (in the formulas (B1) to (B4), Ar 1 , Ar 10 , and Ar 11 each independently represent a trivalent aromatic group which may have a substituent, Ar 2 , Ar 4 , Ar 5 , Ar 7 and Ar 8 each independently represent a divalent aromatic group which may have a substituent, Ar 3 and Ar 6 each independently represent a tetravalent aromatic group which may have a substituent or a group represented by the following formula (II), Ar 9 represents a divalent aromatic group which may have a substituent or a group represented by the following formula (III), X 1 to X 7 each independently represent NRa, O, or S, Ra represents a hydrogen atom, an alkyl group which may have a substituent, or an aryl group, and * represents a bonding site with an adjacent linking group), and (in the formulas (II) and (III), Ar 12 and Ar 13 each independently represent a trivalent aromatic group which may have a substituent, Ar 14 and Ar 15 each independently represent a divalent aromatic group which may have a substituent, Y and Z each independently represent O, S, S(═O) 2 , or CRbRc, Rb and Rc each independently represent a hydrogen atom, an alkyl group which may have a substituent, or an aryl group, and * represents a bonding site with an adjacent linking group), Condition (1): a total content of the groups represented by the formulas (B1) to (B4) is 1% by mass or more and 40% by mass or less with respect to a total amount of the polyimide precursor, and Condition (2): a content of the particles is 5% by mass or more and 90% by mass or less with respect to a total content of the polyimide precursor and the particles.
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