Deprotonation of large calixarenes-cation binding and conformations

© 2016 CSIRO. Single crystal X-ray studies of p-t-butylcalix[10]arene·2dmso·7H2O (1) and [NMe4][p-t-butylcalix[9]arene-H]·2dmso·H2O (2), provide new data on these large macrocycles and their conformations, that of 2 being the first where an encapsulated [NMe4]+ cation is present, while 1 contains th...

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Main Authors: Harrowfield, J., Koutsantonis, G., Ogden, Mark, Sobolev, A., White, A.
Format: Journal Article
Published: CSIRO Publishing 2016
Online Access:http://hdl.handle.net/20.500.11937/18274
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author Harrowfield, J.
Koutsantonis, G.
Ogden, Mark
Sobolev, A.
White, A.
author_facet Harrowfield, J.
Koutsantonis, G.
Ogden, Mark
Sobolev, A.
White, A.
author_sort Harrowfield, J.
building Curtin Institutional Repository
collection Online Access
description © 2016 CSIRO. Single crystal X-ray studies of p-t-butylcalix[10]arene·2dmso·7H2O (1) and [NMe4][p-t-butylcalix[9]arene-H]·2dmso·H2O (2), provide new data on these large macrocycles and their conformations, that of 2 being the first where an encapsulated [NMe4]+ cation is present, while 1 contains the neutral ligand. Both were obtained as crystalline products of the reactions of the calixarenes with tetramethylammonium hydroxide after prolonged standing. The structure of [NEt4][calix[4]arene-H], in which the cation approaches inclusion in the shallow cone of the anion, is also defined and compared with various other alkylammonium derivatives of calixarenes as well as that of p-t-butylcalix[9]arene.
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institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T07:25:04Z
publishDate 2016
publisher CSIRO Publishing
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spelling curtin-20.500.11937-182742017-09-13T13:44:34Z Deprotonation of large calixarenes-cation binding and conformations Harrowfield, J. Koutsantonis, G. Ogden, Mark Sobolev, A. White, A. © 2016 CSIRO. Single crystal X-ray studies of p-t-butylcalix[10]arene·2dmso·7H2O (1) and [NMe4][p-t-butylcalix[9]arene-H]·2dmso·H2O (2), provide new data on these large macrocycles and their conformations, that of 2 being the first where an encapsulated [NMe4]+ cation is present, while 1 contains the neutral ligand. Both were obtained as crystalline products of the reactions of the calixarenes with tetramethylammonium hydroxide after prolonged standing. The structure of [NEt4][calix[4]arene-H], in which the cation approaches inclusion in the shallow cone of the anion, is also defined and compared with various other alkylammonium derivatives of calixarenes as well as that of p-t-butylcalix[9]arene. 2016 Journal Article http://hdl.handle.net/20.500.11937/18274 10.1071/CH15761 CSIRO Publishing fulltext
spellingShingle Harrowfield, J.
Koutsantonis, G.
Ogden, Mark
Sobolev, A.
White, A.
Deprotonation of large calixarenes-cation binding and conformations
title Deprotonation of large calixarenes-cation binding and conformations
title_full Deprotonation of large calixarenes-cation binding and conformations
title_fullStr Deprotonation of large calixarenes-cation binding and conformations
title_full_unstemmed Deprotonation of large calixarenes-cation binding and conformations
title_short Deprotonation of large calixarenes-cation binding and conformations
title_sort deprotonation of large calixarenes-cation binding and conformations
url http://hdl.handle.net/20.500.11937/18274