Convergent heteroditopic cyclo[6]aramides as macrocyclic ion-pair receptors for constructing [2]pseudorotaxanes

Convergent heteroditopic cyclo[6]aramides as macrocyclic ion-pair receptors for constructing [2]pseudorotaxanes

A strategy of using amide groups as the only functionality was developed to construct convergent heteroditopic cyclo[6]aramides that are able to strongly bind dibutylammonium chloride in chloroform (>10(5) M(-1)), leading to the formation of [2]pseudorotaxanes.

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2014-01, Vol.50 (59), p.8024-8027
Hauptverfasser: Hu, Jinchuan, Chen, Long, Shen, Jie, Luo, Jian, Deng, Pengchi, Ren, Yi, Zeng, Huaqiang, Feng, Wen, Yuan, Lihua
Format: Artikel
Sprache:eng
Schlagworte:
Amides
Chlorides
Chloroform
Formations
Macrocyclic compounds
Receptors
Strategy
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container_end_page 8027
container_issue 59
container_start_page 8024
container_title Chemical communications (Cambridge, England)
container_volume 50
creator Hu, Jinchuan
Chen, Long
Shen, Jie
Luo, Jian
Deng, Pengchi
Ren, Yi
Zeng, Huaqiang
Feng, Wen
Yuan, Lihua
description A strategy of using amide groups as the only functionality was developed to construct convergent heteroditopic cyclo[6]aramides that are able to strongly bind dibutylammonium chloride in chloroform (>10(5) M(-1)), leading to the formation of [2]pseudorotaxanes.
doi_str_mv 10.1039/c4cc02557a
format Article
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source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
subjects Amides
Chlorides
Chloroform
Formations
Macrocyclic compounds
Receptors
Strategy
title Convergent heteroditopic cyclo[6]aramides as macrocyclic ion-pair receptors for constructing [2]pseudorotaxanes
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