C4 dissymmetric resorcinarene derivatives: Synthesis, crystal structure and micelle formation

M.J. Mcildowie; M. Mocerino; M.I. Ogden; Brian Skelton; Allan White

doi:10.1007/s10847-015-0525-8

C4 dissymmetric resorcinarene derivatives: Synthesis, crystal structure and micelle formation

M.J. Mcildowie, M. Mocerino, M.I. Ogden, Brian Skelton, Allan White

Research output: Contribution to journal › Article › peer-review

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Abstract

© Springer Science+Business Media Dordrecht 2015. 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.

Original language	English
Pages (from-to)	47-51
Journal	Journal of Inclusion Phenomena and Macrocyclic Chemistry
Volume	82
Issue number	1
DOIs	https://doi.org/10.1007/s10847-015-0525-8
Publication status	Published - 2015

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abstract = "{\textcopyright} Springer Science+Business Media Dordrecht 2015. 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.",

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T1 - C4 dissymmetric resorcinarene derivatives: Synthesis, crystal structure and micelle formation

AU - Mcildowie, M.J.

AU - Mocerino, M.

AU - Ogden, M.I.

AU - Skelton, Brian

AU - White, Allan

PY - 2015

Y1 - 2015

N2 - © Springer Science+Business Media Dordrecht 2015. 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.

AB - © Springer Science+Business Media Dordrecht 2015. 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.

U2 - 10.1007/s10847-015-0525-8

DO - 10.1007/s10847-015-0525-8

M3 - Article

SN - 1388-3127

VL - 82

SP - 47

EP - 51

JO - Journal of Inclusion Phenomena and Macrocyclic Chemistry

JF - Journal of Inclusion Phenomena and Macrocyclic Chemistry

IS - 1

ER -

C4 dissymmetric resorcinarene derivatives: Synthesis, crystal structure and micelle formation

Abstract

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