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Ligand-bridged dinuclear carbonyl compounds of rutheniun and osmium

Includes abstract.

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Bibliographic Details
Main Author: Mushonga, Paul
Other Authors: Moss, John R
Format: Thesis
Language:English
Published: Department of Chemistry 2014
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access_status_str Open Access
author Mushonga, Paul
author2 Moss, John R
author_browse Moss, John R
Mushonga, Paul
author_facet Moss, John R
Mushonga, Paul
author_sort Mushonga, Paul
collection Thesis
description Includes abstract.
format Thesis
id oai:open.uct.ac.za:11427/6348
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:45:27.026Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2014
publishDateRange 2014
publishDateSort 2014
publisher Department of Chemistry
publisherStr Department of Chemistry
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/6348 Ligand-bridged dinuclear carbonyl compounds of rutheniun and osmium Mushonga, Paul Moss, John R Haines, Raymond J Chemistry Includes abstract. Includes bibliographical references (leaves 26-29). Ligand-bridged dinuc1ear carbonyl compounds of ruthenium and osmium have been successfully prepared and characterised by various analytical and spectroscopic techniques. X-ray crystal structures have been determined for the osmium complexes [OS2(CO)4(p-02CCsH4FeCsHs)2L2] {L = PPh3 (102), py (103)}. Some of the complexes were then investigated for their catalytic activity in the oxidation of cyc10hexane and octane. In this work, hydrogen peroxide was used as an oxidant and acetonitrile as the solvent. A higher selectivity for the alcohol products over the ketones was observed. The average ratio of alcohols to ketones was found to be 4.56 and 1.76 for cyc10hexane and octane respectively. The complexes [OS2(CO)6(p-02CMeh] (4) [Ru(CO)2(p-02CMe)2]n (86), [Ru2( CO )4(p-02CMe )(p-dppm h] [PF 6] (117) and [Ru2( CO)4(p -( 02CMe h(MeCN)2] (118), were tested as homogeneous catalysts for the isomerisation of terminal alkenes. Complex 4 was inactive while the complex 118 gave a 100 % conversion. It is proposed that the catalysis proceeded via the displacement of one acetonitrile ligand from the metal centre providing a vacant site onto which the substrate coordinated. The redox behaviour of the four complexes [Ru2(CO)2(p-COh( 2014-08-13T14:27:36Z 2014-08-13T14:27:36Z 2008 Master Thesis Masters MSc http://hdl.handle.net/11427/6348 eng application/pdf Department of Chemistry Faculty of Science University of Cape Town
spellingShingle Chemistry
Mushonga, Paul
Ligand-bridged dinuclear carbonyl compounds of rutheniun and osmium
thesis_degree_str Master's
title Ligand-bridged dinuclear carbonyl compounds of rutheniun and osmium
title_full Ligand-bridged dinuclear carbonyl compounds of rutheniun and osmium
title_fullStr Ligand-bridged dinuclear carbonyl compounds of rutheniun and osmium
title_full_unstemmed Ligand-bridged dinuclear carbonyl compounds of rutheniun and osmium
title_short Ligand-bridged dinuclear carbonyl compounds of rutheniun and osmium
title_sort ligand bridged dinuclear carbonyl compounds of rutheniun and osmium
topic Chemistry
url http://hdl.handle.net/11427/6348
work_keys_str_mv AT mushongapaul ligandbridgeddinuclearcarbonylcompoundsofrutheniunandosmium