Self-assembly of bis-[1]rotaxanes based on diverse thiourea-bridged mono-functionalized dipillar[5]arenes
作者:Lu Yang、Cui-Yun Nie、Ying Han、Jing Sun、Chao-Guo Yan
DOI:10.1007/s10847-021-01103-4
日期:2022.2
pillar[5]arenes with 1,ω-bis(4-isothiocyanatophenoxy)alkanes also afforded diphenoxyalkylene thiourea-bridged dipillar[5]arenes. 1H NMR and NOESY spectra clearly indicated that bis-[1]rotaxanes were formed by insertion of longer alkylene chains into the cavities of two pillar[5]arenes. On the other hand, the free-forms of dipillar[5]arenes were obtained with the shorter ethylene chains existing on the outside
单酰胺官能化柱的缩合反应[5]与芳烃TERE -和异下超声波照射,得到在丙酮-phthaloyl二异硫氰酸酯TERE -和异-phthaloylthiourea-桥接dipillar [5]芳烃。单酰氨基官能化的柱[5]芳烃与1,ω-双(4-异硫氰酸根合苯氧基)烷烃的类似反应也提供了二苯氧基亚烷基硫脲桥连的双柱[5]芳烃。1H NMR 和 NOESY 光谱清楚地表明双-[1] 轮烷是通过将较长的亚烷基链插入两个柱[5] 芳烃的空腔而形成的。另一方面,自由形式的二柱[5]芳烃是在两个柱[5]芳烃的空腔外侧存在较短的乙烯链的情况下获得的。 图形摘要