Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.639774
Title: Single electron transfer reactions and the synthesis of Chiral BODIPYs
Author: Ishaq Lerrick, Reinner
ISNI:       0000 0004 5365 3144
Awarding Body: University of Newcastle Upon Tyne
Current Institution: University of Newcastle upon Tyne
Date of Award: 2014
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Abstract:
This thesis is divided into two parts. Part one covers single electron transfer reactions of electron deficient carbonyls and Grignard reagents whilst part two discusses our progress towards the synthesis of axially chiral BODIPYs. Part 1: Reaction of 2,2,2-trichloro-1-arylethanones with PhMgBr resulted in a reduction to give 2,2-dichloro-1-arylethanones. We have shown through by-product analysis and EPR measurement that this reaction proceeds through a Single Electron Transfer (SET) mechanism with PhMgBr acting as the electron donor. Addition of electrophiles to the intermediate magnesium enolates, formed in the reaction, gave aldol, Claisen and aldol/Tishchenko products. Scheme 1 Reaction of PhMgBr with 2,2,2-trichloro-1-arylethanones followed by addition of an electrophile Scheme 2 General route for the synthesis of axially chiral BODIPYs Resolution of a racemic axially chiral BODIPY was performed by preparative chiral HPLC. Scheme 3 Resolution of racemic-BODIPYs using HPLC Electronic Circular Dichroism (ECD) spectroscopy and measurements showed that the separated BODIPYs were enantiomeric. Comparison of measured and computational ECD spectra allowed assignment of the absolute stereochemistry. Part 2: A number of BODIPYs have been synthesised which demonstrated axial chirality, based on the restricted rotation of ortho-aryl meso substituents.
Supervisor: Not available Sponsor: Indonesian Ministry of National Education
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.639774  DOI: Not available
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