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

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 d...

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Main Authors: Mclldowie, M.J., Mocerino, Mauro, Ogden, Mark, Skelton, B., White, A.H.
Format: Journal Article
Published: Springer Netherlands 2015
Subjects:
Online Access:http://hdl.handle.net/20.500.11937/13394
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author Mclldowie, M.J.
Mocerino, Mauro
Ogden, Mark
Skelton, B.
White, A.H.
author_facet Mclldowie, M.J.
Mocerino, Mauro
Ogden, Mark
Skelton, B.
White, A.H.
author_sort Mclldowie, M.J.
building Curtin Institutional Repository
collection Online Access
description 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.
first_indexed 2025-11-14T07:03:25Z
format Journal Article
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institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T07:03:25Z
publishDate 2015
publisher Springer Netherlands
recordtype eprints
repository_type Digital Repository
spelling curtin-20.500.11937-133942019-02-19T05:34:46Z C4 Dissymmetric resorcinarene derivatives: synthesis, crystal structure and micelle formation Mclldowie, M.J. Mocerino, Mauro Ogden, Mark Skelton, B. White, A.H. Micelles Resorcinarene C4 Dissymmetry Crystal structure 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. 2015 Journal Article http://hdl.handle.net/20.500.11937/13394 10.1007/s10847-015-0525-8 Springer Netherlands fulltext
spellingShingle Micelles
Resorcinarene
C4 Dissymmetry
Crystal structure
Mclldowie, M.J.
Mocerino, Mauro
Ogden, Mark
Skelton, B.
White, A.H.
C4 Dissymmetric resorcinarene derivatives: synthesis, crystal structure and micelle formation
title C4 Dissymmetric resorcinarene derivatives: synthesis, crystal structure and micelle formation
title_full C4 Dissymmetric resorcinarene derivatives: synthesis, crystal structure and micelle formation
title_fullStr C4 Dissymmetric resorcinarene derivatives: synthesis, crystal structure and micelle formation
title_full_unstemmed C4 Dissymmetric resorcinarene derivatives: synthesis, crystal structure and micelle formation
title_short C4 Dissymmetric resorcinarene derivatives: synthesis, crystal structure and micelle formation
title_sort c4 dissymmetric resorcinarene derivatives: synthesis, crystal structure and micelle formation
topic Micelles
Resorcinarene
C4 Dissymmetry
Crystal structure
url http://hdl.handle.net/20.500.11937/13394