Calix[6]arene-based atropoisomeric pseudo[2]rotaxanes

被引:4
|
作者
Gaeta, Carmine [1 ]
Talotta, Carmen [1 ]
Neri, Placido [1 ]
机构
[1] Univ Salerno, Dipartimento Chim & Biol A Zambelli, Via Giovanni Paolo II 132, I-84084 Salerno, Italy
来源
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY | 2018年 / 14卷
关键词
atropoisomers; calixarene; conformation; pseudorotaxane; social isomerism; QUANTUM-MECHANICAL CALCULATIONS; CONFORMATIONALLY RELEVANT H-1; NMR CHEMICAL-SHIFTS; MOLECULAR MACHINES; CALIXARENE; SEQUENCE; CAVITY; COMPLEXATION; WHEEL;
D O I
10.3762/bjoc.14.186
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Some examples of atropoisomeric pseudorotaxanes in which the isomerism arises by the different conformations adopted by the wheel are reported here. Upon threading hexahexyloxycalix[6]arene 1 with ammonium axles 2(+) or 3(+), bearing biphenyl or trifluoromethylbenzyl moieties, respectively, two atropoisomeric pseudorotaxanes were formed in which the calix[6]-wheel 1 adopts the 1,2,3-alternate and cone conformations. The interconversion between them cannot be obtained by simple rotation around the ArCH2Ar bonds of the calixarene wheel, which is blocked by the presence of the axle inside its cavity. Therefore, it can only be obtained through a mechanism of de-threading/re-threading of the axle. In all the examined cases, the 1,2,3-alternate and cone atropoisomers are, respectively, the kinetic and the thermodynamic ones.
引用
收藏
页码:2112 / 2124
页数:13
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