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4,4'-di(3-biphenylyl)biphenyl | 4969-04-4

中文名称
——
中文别名
——
英文名称
4,4'-di(3-biphenylyl)biphenyl
英文别名
1-Phenyl-3-[4-[4-(3-phenylphenyl)phenyl]phenyl]benzene
4,4'-di(3-biphenylyl)biphenyl化学式
CAS
4969-04-4
化学式
C36H26
mdl
——
分子量
458.602
InChiKey
YULFAHGCWJNXGO-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):
    10.1
  • 重原子数:
    36
  • 可旋转键数:
    5
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

点击查看最新优质反应信息

文献信息

  • Polyphenyl synthesis by means of the Kharash-type Grignard cross-coupling reaction.
    作者:EIICHI IBUKI、SHIGERU OZASA、YASUHIRO FUJIOKA、MOTOFUMI OKADA、YOSHIHIKO YANAGIHARA
    DOI:10.1248/cpb.30.2369
    日期:——
    A series of twenty-seven polyphenyls, including quater-to sexiphenyls, was synthesized by the cross-coupling reaction of aryl Grignard reagents with arylene diiodides in the presence of bis (acetylacetonato) nickel (II). Twenty of them were obtained in fairly good yields (50-95%) under mild conditions at temperatures below ca. 60°C in ether-benzene solution within a few hours. In the cases of the remaining seven polyphenyls, however, lower yields (1-34%) were inevitable owing to the sterically crowded geometry of the reactant (s). Thus, the Kharash-type Grignard cross-coupling reaction was proved to be an efficient and convenient method for synthesizing a variety of polyphenyls, except in the cases of reactants with remarkably crowded geometry. The infrared, ultraviolet, and proton magnetic resonance spectral properties of several polyphenyls including three new compounds, 3-(2-biphenylyl)-o-quaterphenyl, 6'-(3-biphenylyl)-m-quaterphenyl, and 3, 4'-di (2-biphenylyl) biphenyl, are presented and discussed.
    合成了一系列二十七种多酚类化合物,包括四苯到六苯,通过芳基格氏试剂芳烃化物在双(乙酰丙酮(II)的存在下进行交叉偶联反应。在温度低于约60°C的醚-苯溶液中,在温和条件下,这二十种化合物的产率相当不错(50-95%),反应时间为几小时。然而,在另外七种多酚类化合物的情况下,由于反应物的立体拥挤几何结构,不可避免地产率较低(1-34%)。因此,Kharash型格氏交叉偶联反应被证明是一种高效且便利的方法用于合成各种多酚类化合物,但在具有显著拥挤几何形状的反应物情况下例外。文中介绍并讨论了包括三个新化合物(3-(2-联苯基)-o-四苯、6'-(3-联苯基)-m-四苯、和3,4'-二(2-联苯基)联苯)在内的几种多酚类化合物的红外、紫外及质子磁共振光谱特性。
  • Studies of Polyphenyls and Polyphenylenes. I. The Syntheses and Infrared and Electronic Spectra of Several Sexiphenyls
    作者:Eiichi Ibuki、Shigeru Ozasa、Kazue Murai
    DOI:10.1246/bcsj.48.1868
    日期:1975.6
    Ullmann reaction of iodobiphenyl and diiodobiphenyl. Infrared studies indicated that the fine structure in the 780–810 cm−1 region suggests the presence of consecutive m-phenylene units, and that the positions of the strong or medium bands in the 820–840 cm−1 region indicate approximately the number of continuous p-phenylene units. The electronic spectra commonly displayed a prominent E-band in the narrow
    通过联苯和二联苯的乌尔曼反应合成了七种线性六联苯。红外研究表明,780-810 cm-1 区域的精细结构表明存在连续的间亚苯基单元,820-840 cm-1 区域中强或中带的位置表明大约有连续对亚苯基单元。电子光谱通常在 192-207 nm 的狭窄区域显示出突出的 E 带。260 nm 以上的强 K 带被认为表明存在一个或多个对亚苯基单元。
  • IBUKI, EIICHI;OZASA, SHIGERU;FUJIOKA, YASUHIRO;OKADA, MOTOFUMI;YANAGIHARA+, CHEM. AND PHARM. BULL., 1982, 30, N 7, 2369-2379
    作者:IBUKI, EIICHI、OZASA, SHIGERU、FUJIOKA, YASUHIRO、OKADA, MOTOFUMI、YANAGIHARA+
    DOI:——
    日期:——
  • IBUKI E.; OZASA S.; MURAI K., BULL. CHEM. SOC. JAP. <BCSJ-A8>, 1975, 48, NO 6, 1868-1874,
    作者:IBUKI E.、 OZASA S.、 MURAI K.
    DOI:——
    日期:——
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