Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/101195
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dc.contributor.authorBurgun, A.-
dc.contributor.authorValente, P.-
dc.contributor.authorEvans, J.-
dc.contributor.authorHuang, D.-
dc.contributor.authorSumby, C.-
dc.contributor.authorDoonan, C.-
dc.date.issued2016-
dc.identifier.citationChemical Communications, 2016; 52(57):8850-8853-
dc.identifier.issn1359-7345-
dc.identifier.issn1364-548X-
dc.identifier.urihttp://hdl.handle.net/2440/101195-
dc.description.abstractThe synthesis and characterisation of two novel, functionalised porous organic cages are presented. We demonstrate that a step-wise approach to the synthesis of these robust C-C bonded cages allows for the introduction of a controlled number of endohedral pyridine functional groups. In addition, kinetic processing is used to access permanently porous morphologies.-
dc.description.statementofresponsibilityAlexandre Burgun, Peter Valente, Jack D. Evans, David M. Huang, Christopher J. Sumby and Christian J. Doonan-
dc.language.isoen-
dc.publisherRoyal Society of Chemistry-
dc.rightsThis journal is © The Royal Society of Chemistry 2016-
dc.source.urihttp://dx.doi.org/10.1039/c6cc04423a-
dc.titleEndohedrally functionalised porous organic cages-
dc.typeJournal article-
dc.identifier.doi10.1039/c6cc04423a-
dc.relation.grantARC-
pubs.publication-statusPublished-
dc.identifier.orcidEvans, J. [0000-0001-9521-2601]-
dc.identifier.orcidHuang, D. [0000-0003-2048-4500]-
dc.identifier.orcidSumby, C. [0000-0002-9713-9599]-
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Chemistry and Physics publications

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