New hydrogen bonding motifs for anion and neutral guest complexation

This thesis presents three different areas of anion or neutral molecule recognition chemistry. There is an extensive study of homoleptic and heteroleptic platinum(II) based receptors for anion recognition. The homoleptic receptor study revealed that urea ligands are more effective than amido-pyrrole...

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Main Author: Fisher, Matthew George
Other Authors: Gale, Philip
Published: University of Southampton 2009
Subjects:
Online Access:https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.509554
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spelling ndltd-bl.uk-oai-ethos.bl.uk-5095542018-09-05T03:24:26ZNew hydrogen bonding motifs for anion and neutral guest complexationFisher, Matthew GeorgeGale, Philip2009This thesis presents three different areas of anion or neutral molecule recognition chemistry. There is an extensive study of homoleptic and heteroleptic platinum(II) based receptors for anion recognition. The homoleptic receptor study revealed that urea ligands are more effective than amido-pyrrole based ligands for binding anions in DMSO solution. Also, isoquinoline based ligands form more stable complexes than pyridine based ligands and their extra rigidity preorganises the receptor for increased anion affinities. The heteroleptic receptor (trans-[Pt(isoquinoline-urea)2(pyridine)2](BF4)2) exhibited either an up-down or up-up conformation in DMSO solution and the solid state, depending on the type and concentration of anion. Two different crystal structures with sulfate revealed formation of both the conformations. The properties of a simple benzimidazole cleft receptor for barbiturates and ureas are reported. Compared to various control analogues, the receptor binds barbital or urea in highly competitive DMSO/MeNO2 solutions. A crystal structure with barbital revealed binding through six hydrogen bonds. The synthesis of a more soluble version of the receptor was attempted. The synthesis of a neutral guest templated catenane was also attempted in an effort to expand on the simple cleft work. Finally, a new triazole strapped calix[4]pyrrole synthesised by ‘click’ chemistry is reported. The receptor shows a high affinity for chloride and bicarbonate in MeCN and DCM solutions. It also exhibits strong lipid bilayer chloride transport properties when compared to the parent meso-octamethylcalix[4]pyrrole. A brief investigation into the use of triptycenes as potential scaffolds for appending hydrogen bond donor groups for anion recognition is also reported.546.3QD ChemistryUniversity of Southamptonhttps://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.509554https://eprints.soton.ac.uk/71836/Electronic Thesis or Dissertation
collection NDLTD
sources NDLTD
topic 546.3
QD Chemistry
spellingShingle 546.3
QD Chemistry
Fisher, Matthew George
New hydrogen bonding motifs for anion and neutral guest complexation
description This thesis presents three different areas of anion or neutral molecule recognition chemistry. There is an extensive study of homoleptic and heteroleptic platinum(II) based receptors for anion recognition. The homoleptic receptor study revealed that urea ligands are more effective than amido-pyrrole based ligands for binding anions in DMSO solution. Also, isoquinoline based ligands form more stable complexes than pyridine based ligands and their extra rigidity preorganises the receptor for increased anion affinities. The heteroleptic receptor (trans-[Pt(isoquinoline-urea)2(pyridine)2](BF4)2) exhibited either an up-down or up-up conformation in DMSO solution and the solid state, depending on the type and concentration of anion. Two different crystal structures with sulfate revealed formation of both the conformations. The properties of a simple benzimidazole cleft receptor for barbiturates and ureas are reported. Compared to various control analogues, the receptor binds barbital or urea in highly competitive DMSO/MeNO2 solutions. A crystal structure with barbital revealed binding through six hydrogen bonds. The synthesis of a more soluble version of the receptor was attempted. The synthesis of a neutral guest templated catenane was also attempted in an effort to expand on the simple cleft work. Finally, a new triazole strapped calix[4]pyrrole synthesised by ‘click’ chemistry is reported. The receptor shows a high affinity for chloride and bicarbonate in MeCN and DCM solutions. It also exhibits strong lipid bilayer chloride transport properties when compared to the parent meso-octamethylcalix[4]pyrrole. A brief investigation into the use of triptycenes as potential scaffolds for appending hydrogen bond donor groups for anion recognition is also reported.
author2 Gale, Philip
author_facet Gale, Philip
Fisher, Matthew George
author Fisher, Matthew George
author_sort Fisher, Matthew George
title New hydrogen bonding motifs for anion and neutral guest complexation
title_short New hydrogen bonding motifs for anion and neutral guest complexation
title_full New hydrogen bonding motifs for anion and neutral guest complexation
title_fullStr New hydrogen bonding motifs for anion and neutral guest complexation
title_full_unstemmed New hydrogen bonding motifs for anion and neutral guest complexation
title_sort new hydrogen bonding motifs for anion and neutral guest complexation
publisher University of Southampton
publishDate 2009
url https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.509554
work_keys_str_mv AT fishermatthewgeorge newhydrogenbondingmotifsforanionandneutralguestcomplexation
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