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Homo- and hetero-[3]rotaxanes with two pi-systems clasped in a single macrocycle.

Abstract:
Here we present the first synthesis of a [3]rotaxane with two dumbbell components threaded through a single gamma-cyclodextrin macrocycle. This synthesis is carried out in two steps: first one dumbbell is synthesized threaded through the macrocycle to give a [2]rotaxane, then a second dumbbell is synthesized through the remaining cavity of the [2]rotaxane. We have synthesized a hetero- [3]rotaxane with one stilbene and one cyanine dye threaded through gamma-cyclodextrin, which exhibits quantitative energy transfer between the two encapsulated dyes. The stilbene [2]rotaxane intermediate in this synthesis has a remarkably high affinity for suitably shaped hydrophobic guests in aqueous solution, facilitating the synthesis of [3]rotaxanes and suggesting possible applications in sensors.
Publication status:
Published

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Publisher copy:
10.1021/ja0665139

Authors

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Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Organic Chemistry
Role:
Author


Journal:
Journal of the American Chemical Society More from this journal
Volume:
128
Issue:
48
Pages:
15374-15375
Publication date:
2006-12-01
DOI:
EISSN:
1520-5126
ISSN:
0002-7863


Language:
English
Pubs id:
pubs:51762
UUID:
uuid:00de5ca0-108c-4fce-a727-0840439edb95
Local pid:
pubs:51762
Source identifiers:
51762
Deposit date:
2012-12-19
ARK identifier:

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