Issue 16, 2011

Pillar[5]arene decaamine: synthesis, encapsulation of very long linear diacids and formation of ion pair-stopped [2]rotaxanes

Abstract

A pillar[5]arene decaamine has been synthesized and revealed to encapsulate linear diacids in neutral, alkaline, and acidic conditions, driven by the hydrophobic and electrostatic interactions, to give rise to pseudo[2]rotaxanes. Ion pair-bonded stoppers can further lock the diacids to generate stable water soluble [2]rotaxanes.

Graphical abstract: Pillar[5]arene decaamine: synthesis, encapsulation of very long linear diacids and formation of ion pair-stopped [2]rotaxanes

Supplementary files

Article information

Article type
Communication
Submitted
01 Feb 2011
Accepted
03 Mar 2011
First published
18 Mar 2011

Chem. Commun., 2011,47, 4694-4696

Pillar[5]arene decaamine: synthesis, encapsulation of very long linear diacids and formation of ion pair-stopped [2]rotaxanes

X. Hu, L. Chen, W. Si, Y. Yu and J. Hou, Chem. Commun., 2011, 47, 4694 DOI: 10.1039/C1CC10633C

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