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2,2'-bis(benzyloxy)-6,6'-bis(4-(diphenylamino)phenyl)-1,1'-binaphthyl | 1312293-42-7

中文名称
——
中文别名
——
英文名称
2,2'-bis(benzyloxy)-6,6'-bis(4-(diphenylamino)phenyl)-1,1'-binaphthyl
英文别名
——
2,2'-bis(benzyloxy)-6,6'-bis(4-(diphenylamino)phenyl)-1,1'-binaphthyl化学式
CAS
1312293-42-7
化学式
C70H52N2O2
mdl
——
分子量
953.195
InChiKey
MNMDHNNAHVLPPW-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):
    19.09
  • 重原子数:
    74.0
  • 可旋转键数:
    15.0
  • 环数:
    12.0
  • sp3杂化的碳原子比例:
    0.03
  • 拓扑面积:
    24.94
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

反应信息

  • 作为产物:
    描述:
    (S)-6,6'-dibromo-1,1'-binaphthalene-2,2'-diol(R)-6,6'-dibromo-2,2'-dibenzyloxy-1,1'-binaphthyl四(三苯基膦)钯potassium carbonate 作用下, 以 甲苯 为溶剂, 反应 24.0h, 以46%的产率得到2,2'-bis(benzyloxy)-6,6'-bis(4-(diphenylamino)phenyl)-1,1'-binaphthyl
    参考文献:
    名称:
    The nature of 6,6′-bis(triphenylamine) substituted BINOL as chromophoric and fluorogenic hybrid chemosensor for selective fluoride detection
    摘要:
    6,6'-Bis(triphenylamine)-1,1'-binaphthy1-2,2'-diol (1) is highly fluorescent in visible region. On treatment with a variety of anions, the UV-vis absorption as well as the fluorescent behavior of 1 in CH2Cl2 is substantially changed. Among the tetrabutylammonium (TBA) salts we tested, including F- OH- (from TBAOH in MeOH), Cl-, Br-, I-, OAc-, HSO4-, TsO- (Et4N salt), and H2PO4-, F- was found to be the most effective fluorescence quencher. Quantitative fluorescence analysis of the titration data revealed that the anions are classified into two categories: (1) Simple mono-anions, such as F- (log beta(F)(2) = 11.00 +/- 0.08), OH- (log beta(OH)(2) = 9.05 +/- 0.01), and Cl- (log beta(2) = 9.96 +/- 0.70) that follow the stoichiometry of 1:2, indicating the formation of (1.X-2)(2-) complexes; (2) Oxo-anions, such as OAc- (log beta(OAc)(1) = 5.13 +/- 0.012), H2PO4- (log beta(HP)(1) = 4.87 +/- 0.03), and TsO- (using tetraethylammonium salt, (log beta(OTs)(1) = 3.36 +/- 0.02) that show the stoichiometry of 1:1, indicating the formation of (1.X)(-) complexes. The complexation behaviors were further confirmed by H-1 NMR spectroscopy. In the co-crystal prepared from 1,1-binaphthy1-2,2'-diol (BINOL) and Et4NF, F- and BINOL are assembled to form a linear polymeric array, with a dimeric group of BINOL/BINOL anions linked as the side-chains. Intramolecular hydrogen bond was observed within the BINOL anion. This provides structural insights about the BINOL-fluoride complex formation. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2011.03.047
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