Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.501900
Title: A new approach to highly reductive neutral organic molecules
Author: Garnier, Jean
Awarding Body: The University of Strathclyde
Current Institution: University of Strathclyde
Date of Award: 2008
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Abstract:
Recently, our research group has been developing novel reactions involving powerful tetraazaalkene-based donors, reducing aryl halides into their corresponding aryl radicals or aryl anions. This thesis reports the development of new powerful donor D, a novel donor structure prepared by a novel route from precursor A. Oxdation of D into diction E provided suitable material for X-ray crystal analysis and electrochemical measurements of the redox potential for the D/E couple. Comparison with other neutral organic electron donors prepared in our group or published by others showed that the bispyridinylidene-based donors presented in this thesis are the isolated organic reagents with the most negative redox potentials recorded to date.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.501900  DOI: Not available
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