Platinum group metal coordination complexes of ferrocenyl N-donor ligands and their potential application in catalysis and medicinal chemistry

 

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dc.contributor.author Rajput, Jaisheila en_ZA
dc.date.accessioned 2014-10-18T06:06:02Z
dc.date.available 2014-10-18T06:06:02Z
dc.date.issued 2003 en_ZA
dc.identifier.citation Rajput, J. 2003. Platinum group metal coordination complexes of ferrocenyl N-donor ligands and their potential application in catalysis and medicinal chemistry. University of Cape Town. en_ZA
dc.identifier.uri http://hdl.handle.net/11427/8616
dc.description Includes bibliographical references. en_ZA
dc.description.abstract In this project a series of multinuclear complexes were successfully prepared and characterised using an array of analytical techniques. The use of nitrogen-donor ligands, in particular pyridine and ferrocenyl derivatives thereof was examined. Two main approaches were taken in the preparation of the ferrocenylpyridines: i. The ferrocenylpyridines were systematically studied by varying the position of substituents along the pyridyl ring in the 4-,3-and 2-positions. ii. The effect of placing spacer groups between the ferrocenyl group and the pendant pyridine was examined. iii. The ligands were prepared with a system of conjugated π bonds, allowing for an electronic pathway within the ligand. en_ZA
dc.language.iso eng en_ZA
dc.subject.other Chemistry en_ZA
dc.title Platinum group metal coordination complexes of ferrocenyl N-donor ligands and their potential application in catalysis and medicinal chemistry en_ZA
dc.type Doctoral Thesis
uct.type.publication Research en_ZA
uct.type.resource Thesis en_ZA
dc.publisher.institution University of Cape Town
dc.publisher.faculty Faculty of Science en_ZA
dc.publisher.department Department of Chemistry en_ZA
dc.type.qualificationlevel Doctoral
dc.type.qualificationname PhD en_ZA
uct.type.filetype Text
uct.type.filetype Image
dc.identifier.apacitation Rajput, J. (2003). <i>Platinum group metal coordination complexes of ferrocenyl N-donor ligands and their potential application in catalysis and medicinal chemistry</i>. (Thesis). University of Cape Town ,Faculty of Science ,Department of Chemistry. Retrieved from http://hdl.handle.net/11427/8616 en_ZA
dc.identifier.chicagocitation Rajput, Jaisheila. <i>"Platinum group metal coordination complexes of ferrocenyl N-donor ligands and their potential application in catalysis and medicinal chemistry."</i> Thesis., University of Cape Town ,Faculty of Science ,Department of Chemistry, 2003. http://hdl.handle.net/11427/8616 en_ZA
dc.identifier.vancouvercitation Rajput J. Platinum group metal coordination complexes of ferrocenyl N-donor ligands and their potential application in catalysis and medicinal chemistry. [Thesis]. University of Cape Town ,Faculty of Science ,Department of Chemistry, 2003 [cited yyyy month dd]. Available from: http://hdl.handle.net/11427/8616 en_ZA
dc.identifier.ris TY - Thesis / Dissertation AU - Rajput, Jaisheila AB - In this project a series of multinuclear complexes were successfully prepared and characterised using an array of analytical techniques. The use of nitrogen-donor ligands, in particular pyridine and ferrocenyl derivatives thereof was examined. Two main approaches were taken in the preparation of the ferrocenylpyridines: i. The ferrocenylpyridines were systematically studied by varying the position of substituents along the pyridyl ring in the 4-,3-and 2-positions. ii. The effect of placing spacer groups between the ferrocenyl group and the pendant pyridine was examined. iii. The ligands were prepared with a system of conjugated π bonds, allowing for an electronic pathway within the ligand. DA - 2003 DB - OpenUCT DP - University of Cape Town LK - https://open.uct.ac.za PB - University of Cape Town PY - 2003 T1 - Platinum group metal coordination complexes of ferrocenyl N-donor ligands and their potential application in catalysis and medicinal chemistry TI - Platinum group metal coordination complexes of ferrocenyl N-donor ligands and their potential application in catalysis and medicinal chemistry UR - http://hdl.handle.net/11427/8616 ER - en_ZA


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