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Synthesis and chemistry of photosphonic derivatives

Dissertation (MSc (Chemistry))--University of Pretoria, 1994.

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Other Authors: Modro, T.A.
Format: Thesis
Language:English
Published: University of Pretoria 2024
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access_status_str Open Access
author2 Modro, T.A.
author_browse Modro, T.A.
author_facet Modro, T.A.
collection Thesis
dc_rights_str_mv © 2024 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria.
description Dissertation (MSc (Chemistry))--University of Pretoria, 1994.
format Thesis
id oai:repository.up.ac.za:2263/99462
institution University of Pretoria (South Africa)
language English
last_indexed 2026-06-10T12:39:46.144Z
license_str Other — see source repository
provenance_str_mv Harvested via OAI-PMH from UPSpace — University of Pretoria Institutional Repository
publishDate 2024
publishDateRange 2024
publishDateSort 2024
publisher University of Pretoria
publisherStr University of Pretoria
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source_str UPSpace — University of Pretoria Institutional Repository
spelling oai:repository.up.ac.za:2263/99462 Synthesis and chemistry of photosphonic derivatives Modro, T.A. Pienaar, Andre Synthesis Chemistry Photosphonic derivatives UCTD Dissertation (MSc (Chemistry))--University of Pretoria, 1994. A reliable method for the preparation of alkylphosphonyl chlorides had to be obtained to prepare precursors for the synthesis of a range of alkylphosphonates which were needed for kinetic studies. Both thionyl chloride and oxalyl chloride were studied as chlorinating agents for phosphonic esters. The use of thionyl chloride together with a catalytic amount of DMF were shown to be of general application in the efficient preparation of phosphonic mono-ester chlorides. A wide range of esters of the formula R2NCH2CH2OPO(R')R", R, R' = CH3, CH2CH3 and R" = OCH3 , OCH2CH3, OCH(CH3) 2 and Cl were synthesized. These compounds were used as substrates to study the kinetics of their unimolecular decomposition. From the relative kinetic data we were able to show that two mechanisms of decomposition were followed depending I on the nature of the leaving group present in the substrate molecule Chemistry MSc (Chemistry) 2024-11-27T09:15:55Z 2024-11-27T09:15:55Z 22/02/04 1994 Dissertation http://hdl.handle.net/2263/99462 en © 2024 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria. application/pdf University of Pretoria
spellingShingle Synthesis
Chemistry
Photosphonic derivatives
UCTD
Synthesis and chemistry of photosphonic derivatives
title Synthesis and chemistry of photosphonic derivatives
title_full Synthesis and chemistry of photosphonic derivatives
title_fullStr Synthesis and chemistry of photosphonic derivatives
title_full_unstemmed Synthesis and chemistry of photosphonic derivatives
title_short Synthesis and chemistry of photosphonic derivatives
title_sort synthesis and chemistry of photosphonic derivatives
topic Synthesis
Chemistry
Photosphonic derivatives
UCTD
url http://hdl.handle.net/2263/99462