Issue 43, 2009

Reverse vesicles formed by hydrogen bonded arylamide-derived triammonium cyclophanes and hexaammonium capsule

Abstract

Hydrogen bonded rigid imine-based macrocycles and capsules have been reduced to cyclic triamines and two-layered hexaamines, the triammonium and hexaammonium derivatives of which are revealed to form reverse vesicles in organic liquids of low polarity, which are characterized by SEM, AFM, (HR)TEM, DLS and XRD.

Graphical abstract: Reverse vesicles formed by hydrogen bonded arylamide-derived triammonium cyclophanes and hexaammonium capsule

Supplementary files

Article information

Article type
Communication
Submitted
14 Jul 2009
Accepted
09 Sep 2009
First published
25 Sep 2009

Chem. Commun., 2009, 6634-6636

Reverse vesicles formed by hydrogen bonded arylamide-derived triammonium cyclophanes and hexaammonium capsule

X. Xu, L. Wang and Z. Li, Chem. Commun., 2009, 6634 DOI: 10.1039/B914030A

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