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Synlett 2007(17): 2609-2626
DOI: 10.1055/s-2007-991078
DOI: 10.1055/s-2007-991078
ACCOUNT
© Georg Thieme Verlag Stuttgart · New York
The Synthesis and Physicochemical and Supramolecular Properties of Strained Phenylacetylene Macrocycles
Further Information
Received
1 May 2007
Publication Date:
27 September 2007 (online)
Publication History
Publication Date:
27 September 2007 (online)
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Abstract
Strained phenylacetylene macrocycles, cyclic [3]- and [4]metaphenylacetylenes ([n]CMPAs) and methoxy derivatives, and cyclic [5]- to [9]paraphenylacetylenes ([n]CPPAs) were prepared using a strategy based on the McMurry coupling reaction. The physicochemical and supramolecular properties of these substances were determined. Interestingly, apart from [3]CMPAs, compounds in these series possess preorganized three-dimensional cavities.
1 Introduction
2 Theoretical Optimized Structures
3 Synthesis
4 Properties and Structures of Cyclic Metaphenylacetylenes
5 Properties and Structures of Carbon Nanorings
6 Outlook
Key words
alkynes - cyclophanes - fullerenes - host-guest systems - McMurry reaction
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