C4 Dissymmetric resorcinarene derivatives: synthesis, crystal structure and micelle formation

Mclldowie, M.J.; Mocerino, Mauro; Ogden, Mark; Skelton, B.; White, A.H.

doi:10.1007/s10847-015-0525-8

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Access Status

Open access

Authors

Mclldowie, M.J.

Mocerino, Mauro

Ogden, Mark

Skelton, B.

White, A.H.

Date

2015

Type

Journal Article

Metadata

Show full item record

Citation

Mclldowie, M.J. and Mocerino, M. and Ogden, M. and Skelton, B. and White, A.H. 2015. C4 Dissymmetric resorcinarene derivatives: synthesis, crystal structure and micelle formation. Journal of Inclusion Phenomena and Macrocyclic Chemistry. 82: pp. 47-51.

Source Title

Journal of Inclusion Phenomena and Macrocyclic Chemistry

DOI

10.1007/s10847-015-0525-8

ISSN

1388-3127

School

Department of Chemistry

Remarks

The final publication is available at Springer via http://doi.org/10.1007/s10847-015-0525-8

URI

http://hdl.handle.net/20.500.11937/13394

Collection

Curtin Research Publications

Abstract

The synthesis of a C4 dissymmetric resorcinarene tetracarboxylic acid derivative and determination of its critical micelle concentration is reported. The tetrahydroxy derivative was prepared by reduction of the tetra-acid. The low-temperature single crystal X-ray structure of the methyl ester derivative of the tetra-acid is also reported. This crystallised with two independent molecules of similar boat (flattened cone) conformation within the asymmetric unit.