摘要
设计、合成了一种新的主体分子2,6-二(α-苯基苄基)-1,5-萘二酚(1).它可与许多有机小分子形成配位包合物.用IR和1HNMR表征了配位包结物,并测定了主客体分子的摩尔比:1?DMF(1∶1),1?DMSO(1∶2),1?吡啶(1∶1),1?喹啉(1∶2),1?N-甲基吡咯烷酮(1∶1).用单晶X衍射分析了包结物(1)?DMF的晶体结构,属三斜晶系,晶胞参数为P-1,a=0.9085(9)nm,b=0.9501(6)nm,c=2.0995(6)nm,α=99.59(3)°,β=90.13(4)°,γ=96.20(7)°,V=1.776(2)nm3,Dc=1.898g?cm-3.结果表明,主体分子间的CH/π弱氢键在决定主体分子的层状框架结构和客体分子在层间的填充方式中发挥了重要作用;两种不等效的客体分子与主体分子的作用方式是不同的,一种客体分子是通过CH/π,CH/O弱氢键与同层的不同主体分子相互作用,另一种是通过CH/π,CH/O弱氢键与相邻层的不同主体分子相互作用.
A new kind of host molecule 2,6-bis（α-phenylbenzyl）-1,5-naphthalenediol （1） was designed and synthesized. It exhibits strong inclusion property with various small organic molecules. The inclusion compounds were characterized by IR and ^1H NMR. The molar ratios of host and guest are I·DMF （1 ： 1）, 1·DMSO （1 ： 2）, 1·pyridine （1 ： 1）, 1·quinoline （1 ： 2） and 1·N-methyl-2-pyrrolidone （1 ： 1）, respectively. The structure of inclusion compound of 1 with DMF was determined by single crystal X-ray diffraction with parameters of triclinic symmetry, P-1, α=0.9085（9） nm, b=0.9501（6） nm, c=2.0995（6） nm, α=99.59（3）°, β=90.13（4）°, γ=96.20（7）°, V=1.776（2）nm^3, Dc=1.898 g·cm^-3. The result showed that CH…π weak hydrogen bonding plays a very important role in constructing the layer host framework and guest molecule packing pattern. The contacts between two inequivalent guests DMF with host are different, and one is through CH…π and CH…O weak hydrogen bonding to the host molecules in the same layer, while the other is through the same interaction in the neighbor layer.
出处
《化学学报》
SCIE
CAS
CSCD
北大核心
2005年第16期1525-1530,共6页
Acta Chimica Sinica
基金
国家自然科学基金(No.20372031)资助项目.
