Synthesis of novel benzimidazole derivatives and their platinum (II) complexes.

Imidazo[1,5-a]pyridines are an important and versatile class of N-heterocyclic compounds due to their stability, unique biological, and photochemical properties. Due to the conjugation and charged structure, their properties are extended to conducting electricity and also have electronic properti...

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Other Authors: Soares, A. M.
Language:en
Published: 2011
Subjects:
Online Access:http://hdl.handle.net/10413/2612
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spelling ndltd-netd.ac.za-oai-union.ndltd.org-ukzn-oai-http---researchspace.ukzn.ac.za-10413-26122014-02-08T03:48:57ZSynthesis of novel benzimidazole derivatives and their platinum (II) complexes.Imidazoles--Synthesis.Imidazopyridines.Heterocyclic compounds.Chemistry--Theses.Pyridine.Imidazo[1,5-a]pyridines are an important and versatile class of N-heterocyclic compounds due to their stability, unique biological, and photochemical properties. Due to the conjugation and charged structure, their properties are extended to conducting electricity and also have electronic properties. They can be used for chelating transition metals especially heavy metals that can be harmful to living things (including human). The aim of this research was to develop more useful imidazo[1,5-a]pyridines which are stable in both free and complexed state. A variety of imidazo[1,5-a]pyridyl compounds was synthesized following three useful methods namely (i) The first route includes the isolation of imine intermediates which were then treated with phosphorus oxychloride in one case and hydrochloric acid in another case as catalysts. Both cases resulted in the yield of the same imidazo[1,5-a]pyridyl compounds. (ii) The second route was the development on the first route for those imine intermediates that could not be isolated and only hydrochloric acid catalyst was used. In both the first and second routes, paraformaldehyde was used for the ringclosure step of the reaction. The last route for the formation of imidazo[1,5-a]pyridyl compounds did not involve the use of the paraformaldehyde reagent. The suitable routes were followed depending on the nature of the targeted products and the reaction yields were moderate to excellent.Thesis (M.Sc.)-University of KwaZulu-Natal, Pietermaritzburg,2010.Soares, A. M.2011-03-04T10:24:17Z2011-03-04T10:24:17Z20102010Thesishttp://hdl.handle.net/10413/2612en
collection NDLTD
language en
sources NDLTD
topic Imidazoles--Synthesis.
Imidazopyridines.
Heterocyclic compounds.
Chemistry--Theses.
Pyridine.
spellingShingle Imidazoles--Synthesis.
Imidazopyridines.
Heterocyclic compounds.
Chemistry--Theses.
Pyridine.
Synthesis of novel benzimidazole derivatives and their platinum (II) complexes.
description Imidazo[1,5-a]pyridines are an important and versatile class of N-heterocyclic compounds due to their stability, unique biological, and photochemical properties. Due to the conjugation and charged structure, their properties are extended to conducting electricity and also have electronic properties. They can be used for chelating transition metals especially heavy metals that can be harmful to living things (including human). The aim of this research was to develop more useful imidazo[1,5-a]pyridines which are stable in both free and complexed state. A variety of imidazo[1,5-a]pyridyl compounds was synthesized following three useful methods namely (i) The first route includes the isolation of imine intermediates which were then treated with phosphorus oxychloride in one case and hydrochloric acid in another case as catalysts. Both cases resulted in the yield of the same imidazo[1,5-a]pyridyl compounds. (ii) The second route was the development on the first route for those imine intermediates that could not be isolated and only hydrochloric acid catalyst was used. In both the first and second routes, paraformaldehyde was used for the ringclosure step of the reaction. The last route for the formation of imidazo[1,5-a]pyridyl compounds did not involve the use of the paraformaldehyde reagent. The suitable routes were followed depending on the nature of the targeted products and the reaction yields were moderate to excellent. === Thesis (M.Sc.)-University of KwaZulu-Natal, Pietermaritzburg,2010.
author2 Soares, A. M.
author_facet Soares, A. M.
title Synthesis of novel benzimidazole derivatives and their platinum (II) complexes.
title_short Synthesis of novel benzimidazole derivatives and their platinum (II) complexes.
title_full Synthesis of novel benzimidazole derivatives and their platinum (II) complexes.
title_fullStr Synthesis of novel benzimidazole derivatives and their platinum (II) complexes.
title_full_unstemmed Synthesis of novel benzimidazole derivatives and their platinum (II) complexes.
title_sort synthesis of novel benzimidazole derivatives and their platinum (ii) complexes.
publishDate 2011
url http://hdl.handle.net/10413/2612
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