2,2'-二乙炔基-1,1'-联萘为模板构筑的新的环芳化合物的合成及其光学性质

基于2,2'-二取代的联萘衍生物在手性构型上高度稳定的特点,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2个有趣的拓扑环芳分子四联萘笼状对映异构体(R,R,R,R)-2和(S,S,S,S)-2.其合成路线涉及保护基的控制导入、苯连接桥的链接、保护基的脱去以及偶合成环反应4个步骤.用MS,IR,UV-Vis,1HNMR,13CNMR和元素分析等技术对其进行了表征,并比较了其光学性质.研究结果表明,采用这种模板合成方法能够有效地获得具有单一手性的目标化合物.镜像特征的圆二色(CD)谱和比旋光度α]D的测定结果清楚地反映了它们的对映异构关系.

Synthesis of Novel Enantiomers Cyclophanes Using 2,2′-Diethynyl-1,1′-binaphthyls as a Structural Block and Their Optical Properties

We employed (R)- and (S)-2,2'-diethynyl-1,1'-binaphthyl with a highly stable chirality as the structural blocks and investigated the synthesis of two topologically interesting tetrabinaphthyl cage compounds (R,R,R,R)-2 and (S,S,S,S)-2 via the multi steps reactions including the introduction of protecting group, linking of benzene-bridge, removal of protecting group as well as intermolecular cross-coupling. As expected, the results from MS, IR, UV-Vis, 1H, 13CNMR, elemental analysis and optical properties indicate that this method is very effective for obtaining compound 2 in enantiomer form. The enantiomer relation of the two isomers was reflected unambiguously by their circular dichroism(CD) spectra with exact mirror images and specific rotations α]D data.