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一种含有手性联萘“铰链”单元的环芳分子的设计、合成及表征
引用本文:安德烈,陈燕桂,张英俊,陈强,张志扬,严宏,孟桂英,赵文应,于正英.一种含有手性联萘“铰链”单元的环芳分子的设计、合成及表征[J].化学学报,2006,64(14):1465-1473.
作者姓名:安德烈  陈燕桂  张英俊  陈强  张志扬  严宏  孟桂英  赵文应  于正英
作者单位:(湖南大学化学化工学院 长沙 410082)
基金项目:国家自然科学基金;高等学校博士学科点专项科研项目
摘    要:基于联萘衍生物手性构型高度稳定以及联萘结构中2个萘平面的两面角可以在一定范围内张合的特点, 分别以光学活性的(R)和(S)-2,2'-二乙炔基-1,1'-联萘为模板, 设计了一种含有8个“铰链”结构单元的新的环芳分子¾—(R,R,R,R,R,R,R,R)-3和(S,S,S,S,S,S,S,S)-3. 其合成路线涉及间苯基连接桥的链接, 保护基的脱去和控制导入以及分子间偶合等步骤. 用MS, IR, UV-Vis, 1H和13C NMR以及元素分析等技术对中间体和目标化合物进行了结构表征. 测定并比较了2个目标化合物的比旋光度α]D和圆二色(CD)性质. 在CH2Cl2溶液中, 两个异构体(R,R,R,R,R,R,R,R)-3和(S,S,S,S,S,S,S,S)-3的α]D25值分别为-911.8和+908.6, 并且它们的CD谱表现出对称的镜像特征.这些实验结果清楚地反映了它们之间的对映异构关系.

关 键 词:光学活性  联萘模板  环芳化合物  对映异构体  合成  
收稿时间:12 22 2005 12:00AM
修稿时间:2005-12-222006-03-28

Design, Synthesis and Characterization of a New Type of Cyclo-phane Containing Chiral Binaphthyls as Hinges Units
AN,De-Lie,CHEN,Yan-Gui,ZHANG,Ying-Jun,CHEN,Qiang,ZHANG,Zhi-Yang,YAN,Hong,MENG,Gui-Ying,ZHAO,Wen-Ying,YU,Zheng-Ying.Design, Synthesis and Characterization of a New Type of Cyclo-phane Containing Chiral Binaphthyls as Hinges Units[J].Acta Chimica Sinica,2006,64(14):1465-1473.
Authors:AN  De-Lie  CHEN  Yan-Gui  ZHANG  Ying-Jun  CHEN  Qiang  ZHANG  Zhi-Yang  YAN  Hong  MENG  Gui-Ying  ZHAO  Wen-Ying  YU  Zheng-Ying
Institution:(College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082)
Abstract:Based on highly stable chiral configuration of binaphthyls and behavior of extension/contraction of the dihedral angle between the two naphthalene rings in binaphthyl, we have designed two cyclophane enantiomers (R,R,R,R,R,R,R,R)-3 and (S,S,S,S,S,S,S,S)-3 containing eight chiral binaphthyl units by utilizing (R) and (S)-2,2'-diethynyl-1,1'-binaphthyl as hinges template, respectively. The synthetic procedure involved the multi steps reactions including the linking of meta-substituted benzene-bridge, removal and control introduction of protecting group, as well as intermolecular cross-coupling, etc. MS, IR, 1H and 13C NMR as well as elemental analysis characterized intermediates and target compound 3. The specific rotations (α]D) of two isomers in CH2Cl2 are -911.8 and +908.6, and their circular dichroism (CD) spectra represented exactly mirror images of each other. These results reflected unambiguously enantiomeric relation between two optically pure isomers.
Keywords:chirality  binaphthyl template  cyclophane  enantiomer  synthesis
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