Synthetic routes to Bis-Calix [n]areness : a thesis presented in partial fulfilment of the requirements for the degree of Masterate of Science in Chemistry at Massey University

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dc.contributor.authorIrwin, Jacob Lawrence
dc.date.accessioned2018-09-07T03:00:15Z
dc.date.available2018-09-07T03:00:15Z
dc.date.issued1997
dc.description.abstractThe literature procedures for the targeted syntheses of p-tert-butylcalix[4]arene, p-tert-butylcalix[5]arene, p-tert-butylcalix[6]arene, p-tert-butylcalix[7]arene, and p-tert-butylcalix[8]arene have been repeated successfully. In the case of p-tert-butylcalix[4]arene, alterations led to a less capricious procedure, synthesis of the pure product directly and in higher yield. The residual xylene and toluene solutions from the targeted p-tert-butylcalix[8]arene preparation were utilised to obtain workable quantities of the rare calix[5]- and calix[7]arenes, a protocol that is far simpler and less time-consuming than the low-yielding targeted synthesis of these compounds. Dealkylation of p-tert-butylcalix[n]arenes is best accomplished at 30°C in 0.16-0.05 molL−¹ toluene solution. The insolubility of calix[8]arene in all common organic solvents is expected to limit its synthetic use. Two new protocols have been devised for the highly selective mono-O-alkylation of calixarenes 4 through 8. This work represents the realisation of the first selective functionalisation methods that are applicable to the calixarene family, and also the first selective functionalisation of a calix[7]arene. These findings will lead to more efficient synthesis of multiple calixarenes (cf. Chapter 3) and may allow for a better understanding of the reasons for selectivity in calixarene-O-alkylations. We have been able to synthesise a variety of bis-calixarenes by two different routes. Glaser-Hay coupling allowed the synthesis of symmetrical diyne bridged bis-calix[4, 6 and 8]arenes in high yield. Extension of the first general mono-O-alkylation procedure for calixarenes has made it possible to synthesise hom o-bis-calixarenes in good yield in one step from the parent calixarenes. The unexpected formation of monobromoxylyl calixarenes allows the prospect of the synthesis of hetero-bis-calixarenes under more forcing conditions. Most importantly this allows us to further explore the chemistry of bis-calixarenes by making them readily available (in large quantities) for more elaborate syntheses.en_US
dc.identifier.urihttp://hdl.handle.net/10179/13760
dc.identifier.wikidataQ112852171
dc.identifier.wikidata-urihttps://www.wikidata.org/wiki/Q112852171
dc.language.isoenen_US
dc.publisherMassey Universityen_US
dc.rightsThe Authoren_US
dc.subjectCalixarenes -- Synthesisen_US
dc.titleSynthetic routes to Bis-Calix [n]areness : a thesis presented in partial fulfilment of the requirements for the degree of Masterate of Science in Chemistry at Massey Universityen_US
dc.typeThesisen_US
massey.contributor.authorIrwin, Jacob Lawrence
thesis.degree.disciplineChemistryen_US
thesis.degree.grantorMassey Universityen_US
thesis.degree.levelMastersen_US
thesis.degree.nameMaster of Science (M. Sc.)en_US
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