Issue 5, 2011
From the journal:

Chemical Communications

Arranging pseudorotaxanes octahedrally around [60]fullerene†

Sanjeev K. Dey,a   Florian Beuerle,a   Mark A. Olsona  and  J. Fraser Stoddart*a  

* Corresponding authors

a Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208, USA
E-mail: stoddart@northwestern.edu
Fax: +1 (847) 491 1009
Tel: +1 (847) 491 3793

Abstract

The formation of both [2]- and [7]pseudorotaxanes, which are obtained by mixing of a dibenzylammonium derivative with mono- and hexakis-adducts of [60]fullerene bearing malonato-benzo[25]crown-8 rings, has been monitored in dichloromethane by both 1D and 2D 1H NMR spectroscopies.

Graphical abstract: Arranging pseudorotaxanes octahedrally around [60]fullerene

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Article information

DOI
https://doi.org/10.1039/C0CC03963B
Article type
Communication
Submitted
19 Sep 2010
Accepted
11 Oct 2010
First published
03 Dec 2010

Chem. Commun., 2011,47, 1425-1427

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Arranging pseudorotaxanes octahedrally around [60]fullerene

S. K. Dey, F. Beuerle, M. A. Olson and J. F. Stoddart, Chem. Commun., 2011, 47, 1425 DOI: 10.1039/C0CC03963B

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