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Dipyrromethane based receptors for anions

Dipyrromethane based receptors for anions
Dipyrromethane based receptors for anions
This thesis is principally concerned with the synthesis of a range of dipyrromethane based receptors and their ability to bind anions, in particular carboxylates of amino acid derivatives.
Chapter I provides a general introduction to the field of Supramolecular Chemistry and its applications. In this chapter a series of receptors for anions are presented their properties discussed. A particular attention is given to the aromatic heterocycles based receptors and to enantioselective receptors.
Chapter II describes the synthesis of a series of acyclic receptors which are the results of subsequent modifications of a simple tweezer, based on a dipyrromethane unit coupled with two butyl amines, previously studied by the group.1 The binding properties with a series of anions are presented and, for the chiral receptors, the binding properties with Nprotected amino acids were investigated.
Chapter III describes the synthesis and the binding properties of a series of macrocycles obtained by modifications of the tweezer receptors. The binding properties of the macrocyclic receptors with a series of anions and amino acids are also presented.
Allasia, Sara
1d003a03-08a3-44cf-b5b3-56ee0510ac0f
Allasia, Sara
1d003a03-08a3-44cf-b5b3-56ee0510ac0f
Gale, Philip
c840b7e9-6847-4843-91af-fa0f8563d943

Allasia, Sara (2008) Dipyrromethane based receptors for anions. University of Southampton, School of Chemistry, Doctoral Thesis, 252pp.

Record type: Thesis (Doctoral)

Abstract

This thesis is principally concerned with the synthesis of a range of dipyrromethane based receptors and their ability to bind anions, in particular carboxylates of amino acid derivatives.
Chapter I provides a general introduction to the field of Supramolecular Chemistry and its applications. In this chapter a series of receptors for anions are presented their properties discussed. A particular attention is given to the aromatic heterocycles based receptors and to enantioselective receptors.
Chapter II describes the synthesis of a series of acyclic receptors which are the results of subsequent modifications of a simple tweezer, based on a dipyrromethane unit coupled with two butyl amines, previously studied by the group.1 The binding properties with a series of anions are presented and, for the chiral receptors, the binding properties with Nprotected amino acids were investigated.
Chapter III describes the synthesis and the binding properties of a series of macrocycles obtained by modifications of the tweezer receptors. The binding properties of the macrocyclic receptors with a series of anions and amino acids are also presented.

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Published date: October 2008
Organisations: University of Southampton

Identifiers

Local EPrints ID: 67198
URI: http://eprints.soton.ac.uk/id/eprint/67198
PURE UUID: 1f321b80-e57a-41fd-a944-26e5336598d7
ORCID for Philip Gale: ORCID iD orcid.org/0000-0001-9751-4910

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Date deposited: 07 Aug 2009
Last modified: 14 Mar 2024 02:44

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Contributors

Author: Sara Allasia
Thesis advisor: Philip Gale ORCID iD

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