Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.343542
Title: Synthesis, structure determination and mechanism in thiophene derivatives
Author: Weddell, Derek Alexander
ISNI:       0000 0001 3565 2074
Awarding Body: Nottingham Trent University
Current Institution: Nottingham Trent University
Date of Award: 2001
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Abstract:
A series of O₂N₂ and O₃N₂ macrocycles incorporating thiophene have been prepared. Various carbon chain lengths exist between the donor atoms (nitrogen or oxygen) giving a range of macrocycles with ring sizes varying from 14 to 20 atoms. Semi-large scale synthesis (circa 50 g) was carried out on the production of α,ω-bis(3-oxythienyl)alkanes from the starting material methyl 3-hydroxythiophene-2-caiboxylate. A series of N,N'-bis-(R,R'-benzyl)-alkane-diamine compounds was also synthesised on a semi-large scale. The aminomethylation of thiophene (the Mannich reaction) was used to facilitate the production of thiophene-based macrocycles from the mentioned starting material without resorting to elaborate purification techniques. Thiophene-based macrocycles (where R = NH₂) were appended to a polymeric support (a Merrifield based resin). Competition ring formation has been found during some Mannich reactions, in some cases preventing effective synthesis of the intended macrocycles. Along with observations, some limitations to ring formation using the Mannich reaction arc discussed. The X-ray crystallographic data for a 15-membered thiophene-based macrocycle is presented together with discussion of its geometry. Intramolecular non-bonded contacts between nitrogen and phenyl-H explain the unexpected geometry of this compound. The calculation of the bonding cavity size of this 15-membered macrocycle along with metal-ion binding studies are discussed.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.343542  DOI: Not available
Keywords: Macrocycles; Donor atoms; Ring formation
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