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dc.contributor.authorBAKER, ROBERT JAMES
dc.date.accessioned2012-06-18T11:18:05Z
dc.date.available2012-06-18T11:18:05Z
dc.date.issued2012
dc.date.submitted2012en
dc.identifier.citationM. Ikram and R.J. Baker, Fluorous Catalyst Recycling Utilising Highly Fluorinated Zinc Compounds: Ring Opening Polymerisation of e-Caprolactone, Journal of Fluorine Chemistry, 139, 2012, 58 - 62en
dc.identifier.otherY
dc.descriptionPUBLISHEDen
dc.description.abstractThe synthesis of highly fluorinated zinc carboxylates, [{CF3(CF2)5CH2CH2CO2}2Zn], and alkoxides, [{CF3(CF2)5CH2CH2O}2Zn(OEt2)2] and their use as catalysts for the ring opening polymerisation of ?-caprolactone are described. Quenching the polymerisation reaction with fluorous acids or alcohols regenerates the catalyst which can be recovered by fluorous solvent extractions and the catalytic activity is retained for three cycles. The superior recyclability of the alkoxide to the carboxylate zinc compound is due to the greater partition coefficient between fluorous and organic solvents. Also investigated is the well defined aryloxide compound [(ArO)2Zn(THF)2] which yields very well controlled polymerisation, but cannot be recycled by quenching with a fluorous alcohol.en
dc.format.extent58en
dc.format.extent62en
dc.language.isoenen
dc.publisherElsevieren
dc.relation.ispartofseriesJournal of Fluorine Chemistry;139
dc.rightsYen
dc.subjectChemistryen
dc.subjectRing Opening Polymerisationen
dc.subjectPerfluorinated Alcoholsen
dc.subjectZinc Alkoxidesen
dc.titleFluorous Catalyst Recycling Utilising Highly Fluorinated Zinc Compounds: Ring Opening Polymerisation of e-Caprolactoneen
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/bakerrj
dc.identifier.rssinternalid78518
dc.identifier.rssurihttp://dx.doi.org/10.1016/j.jfluchem.2012.04.004en
dc.identifier.urihttp://hdl.handle.net/2262/63760


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