Ruthenium (II) polyaza-cavity complexes as structural and photochemical probes of electron transfer reactivity

A ruthenium(I I) bis (triflate) (CTf) is used to synthesise polyaza-cavity ruthenium species. Ligands, formally derived -from phenanthroline are coordinated to give mixed ligand complexes. Isolated as hexafluorophosphate salts, these complexes are characterised by elemental analysis, proton N.M.R.,...

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Main Author: Yearwood, G.D.
Format: Thesis
Language:English
Published: 1992
Subjects:
Online Access:https://openaccess.city.ac.uk/id/eprint/28577/
https://openaccess.city.ac.uk/id/eprint/28577/1/Yearwood%20thesis%201990%20PDF-A.pdf
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spelling ftcityunivlondon:oai:openaccess.city.ac.uk:28577 2023-07-02T03:33:47+02:00 Ruthenium (II) polyaza-cavity complexes as structural and photochemical probes of electron transfer reactivity Yearwood, G.D. 1992 text https://openaccess.city.ac.uk/id/eprint/28577/ https://openaccess.city.ac.uk/id/eprint/28577/1/Yearwood%20thesis%201990%20PDF-A.pdf en eng https://openaccess.city.ac.uk/id/eprint/28577/1/Yearwood%20thesis%201990%20PDF-A.pdf Yearwood, G.D. (1992). Ruthenium (II) polyaza-cavity complexes as structural and photochemical probes of electron transfer reactivity. (Unpublished Doctoral thesis, City, University of London) QD Chemistry Thesis NonPeerReviewed 1992 ftcityunivlondon 2023-06-13T18:43:00Z A ruthenium(I I) bis (triflate) (CTf) is used to synthesise polyaza-cavity ruthenium species. Ligands, formally derived -from phenanthroline are coordinated to give mixed ligand complexes. Isolated as hexafluorophosphate salts, these complexes are characterised by elemental analysis, proton N.M.R., infra-red, FAB-mass spectrometry and uv/visible absorption spectroscopy. In an attempt to investigate the tuning of the excited state potential of these complexes, luminescence photochemical data are presented. Results for the mononuclear metallo-complexes indicate substituents to tris (1,10- mhenanthroline) coordination spheres merely alter non-radiative decay rates. Tuning of the excited state is only observed upon alteration of the ligator's magnitude of d level splitting. Dinuclear complexes are shown to possess exciting characteristics required for tailored excited state species. Proton N.M.R. is used to illustrate the presence of diastereomers for the complex, tetrakis (1,10-phenanthroline) [ -3,6-bis (2'-pyridyl)-1,2,4,5-tetrazine] diruthenium(II) tetrakis (hexafluorophosphate), C28. Dramatic solvent sensitivity is also demonstrated by the luminescent C28. Distance dependence of electron transfer is investigated by derivatisation of sperm whale myoglobin with polyaza-cavity ruthenium complexes. Analysis of the conjugate obtained with bis (1,10-phenanthroline) [4-(p -chlorosulphonyl) pheny1-1,10-phenanthroline] rutheniurn (II) , C27, gives the through space electron transfer rate, as 3.0x10* s~1. Assuming the distance between the rutheniurn (II) and iron (III) centres to be 25(+2 A) , the coupling coefficient,β, is found to be between 0.8 and 1.0. This was lower than expected for a protein matrix, suggesting a coupling enhancement effect. A new metallo-protein is prepared by affinity labelling of chymotrypsin with a ruthenated L-phenylalanine chloromethylketone derivative, C24. Perturbation of the semi-synthetic systems excited state is tentatively ascribed to the presence of disulphide bonds in the ... Thesis Sperm whale City University London: City Research Online
institution Open Polar
collection City University London: City Research Online
op_collection_id ftcityunivlondon
language English
topic QD Chemistry
spellingShingle QD Chemistry
Yearwood, G.D.
Ruthenium (II) polyaza-cavity complexes as structural and photochemical probes of electron transfer reactivity
topic_facet QD Chemistry
description A ruthenium(I I) bis (triflate) (CTf) is used to synthesise polyaza-cavity ruthenium species. Ligands, formally derived -from phenanthroline are coordinated to give mixed ligand complexes. Isolated as hexafluorophosphate salts, these complexes are characterised by elemental analysis, proton N.M.R., infra-red, FAB-mass spectrometry and uv/visible absorption spectroscopy. In an attempt to investigate the tuning of the excited state potential of these complexes, luminescence photochemical data are presented. Results for the mononuclear metallo-complexes indicate substituents to tris (1,10- mhenanthroline) coordination spheres merely alter non-radiative decay rates. Tuning of the excited state is only observed upon alteration of the ligator's magnitude of d level splitting. Dinuclear complexes are shown to possess exciting characteristics required for tailored excited state species. Proton N.M.R. is used to illustrate the presence of diastereomers for the complex, tetrakis (1,10-phenanthroline) [ -3,6-bis (2'-pyridyl)-1,2,4,5-tetrazine] diruthenium(II) tetrakis (hexafluorophosphate), C28. Dramatic solvent sensitivity is also demonstrated by the luminescent C28. Distance dependence of electron transfer is investigated by derivatisation of sperm whale myoglobin with polyaza-cavity ruthenium complexes. Analysis of the conjugate obtained with bis (1,10-phenanthroline) [4-(p -chlorosulphonyl) pheny1-1,10-phenanthroline] rutheniurn (II) , C27, gives the through space electron transfer rate, as 3.0x10* s~1. Assuming the distance between the rutheniurn (II) and iron (III) centres to be 25(+2 A) , the coupling coefficient,β, is found to be between 0.8 and 1.0. This was lower than expected for a protein matrix, suggesting a coupling enhancement effect. A new metallo-protein is prepared by affinity labelling of chymotrypsin with a ruthenated L-phenylalanine chloromethylketone derivative, C24. Perturbation of the semi-synthetic systems excited state is tentatively ascribed to the presence of disulphide bonds in the ...
format Thesis
author Yearwood, G.D.
author_facet Yearwood, G.D.
author_sort Yearwood, G.D.
title Ruthenium (II) polyaza-cavity complexes as structural and photochemical probes of electron transfer reactivity
title_short Ruthenium (II) polyaza-cavity complexes as structural and photochemical probes of electron transfer reactivity
title_full Ruthenium (II) polyaza-cavity complexes as structural and photochemical probes of electron transfer reactivity
title_fullStr Ruthenium (II) polyaza-cavity complexes as structural and photochemical probes of electron transfer reactivity
title_full_unstemmed Ruthenium (II) polyaza-cavity complexes as structural and photochemical probes of electron transfer reactivity
title_sort ruthenium (ii) polyaza-cavity complexes as structural and photochemical probes of electron transfer reactivity
publishDate 1992
url https://openaccess.city.ac.uk/id/eprint/28577/
https://openaccess.city.ac.uk/id/eprint/28577/1/Yearwood%20thesis%201990%20PDF-A.pdf
genre Sperm whale
genre_facet Sperm whale
op_relation https://openaccess.city.ac.uk/id/eprint/28577/1/Yearwood%20thesis%201990%20PDF-A.pdf
Yearwood, G.D. (1992). Ruthenium (II) polyaza-cavity complexes as structural and photochemical probes of electron transfer reactivity. (Unpublished Doctoral thesis, City, University of London)
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