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dc.contributor.advisorKilian, Petr
dc.contributor.authorArmstrong, Kenneth Mark
dc.coverage.spatial192en_US
dc.date.accessioned2012-05-08T13:23:02Z
dc.date.available2012-05-08T13:23:02Z
dc.date.issued2011-11-22
dc.identifieruk.bl.ethos.552594
dc.identifier.urihttp://hdl.handle.net/10023/2587
dc.description.abstractTriaryl phosphates were synthesized from white phosphorus and phenols in aerobic conditions and in the presence of iron catalysts and iodine. Full conversion to phosphates was achieved without the use of chlorine or chlorinated solvents, and the reactions do not produce acid waste. Triphenyl phosphate, tritolyl phosphate and tris(2,4-di-tert-butyl)phenyl phosphate were synthesized by this method with 100% conversion from P₄. Various iron(III) diketonates were used to catalyse the conversion. Mechanistic studies showed the reaction to proceed via the formation of phosphorus triiodide (PI₃), then diphenyl phosphoroiodidate (O=PI(OPh)₂) before the final formation of triphenyl phosphate (O=P(OPh)₃). The nucleophilic substitution of O=PI(OPh)₂ with phenol to form O=P(OPh)₃ was found to be the rate determining step. It was found that by modifying the reaction conditions the same catalytic systems could be used to synthesize triphenyl phosphite directly from P₄. Triphenyl phosphite was synthesized in selectivities of up to 60 %. The mechanism of these transformations was also elucidated. Independent syntheses of the intermediate in the reaction mechanism, O=P(OPh)₂I and its hydrolysis products diphenyl phosphate (O=P(OPh)₂OH) and tetraphenyl pyrophosphate ((O)P(OPh)₂-O-P(O)(OPh)₂) were developed from PI₃. The 2,4-di-tert-butyl phenol analogues of these compounds were also prepared. Bis-(2,4-di-tert-butylphenyl) phosphoroiodidate was then reacted with various alcohols to produce a series of mixed triorgano phosphates.en_US
dc.language.isoenen_US
dc.publisherUniversity of St Andrews
dc.subjectGreen chemistryen_US
dc.subjectCatalysisen_US
dc.subjectWhite phosphorusen_US
dc.subjectPhosphatesen_US
dc.subject.lccQD305.P46A8en_US
dc.subject.lcshOrganophosphorus compounds--Synthesisen_US
dc.subject.lcshPhosphorusen_US
dc.subject.lcshIron catalystsen_US
dc.titleCatalytic synthesis of organophosphate plastics additives from white phosphorusen_US
dc.typeThesisen_US
dc.contributor.sponsorThermphos International; EPSRCen_US
dc.type.qualificationlevelDoctoralen_US
dc.type.qualificationnamePhD Doctor of Philosophyen_US
dc.publisher.institutionThe University of St Andrewsen_US


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