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dc.contributor.authorLau, Cher Hon
dc.contributor.authorLu, Tian-dan
dc.contributor.authorSun, Shi-Peng
dc.contributor.authorChen, Xianfeng
dc.contributor.authorCarta, Mariolino
dc.contributor.authorDawson, Daniel M.
dc.date.accessioned2019-07-09T11:30:06Z
dc.date.available2019-07-09T11:30:06Z
dc.date.issued2019-07-28
dc.identifier259544982
dc.identifierfc5c6d5b-9480-4003-8e8f-261a4fb9b72d
dc.identifier000476609500010
dc.identifier85069475794
dc.identifier.citationLau , C H , Lu , T , Sun , S-P , Chen , X , Carta , M & Dawson , D M 2019 , ' Continuous flow knitting of a triptycene hypercrosslinked polymer ' , Chemical Communications , vol. 55 , no. 59 , pp. 8571-8574 . https://doi.org/10.1039/C9CC03731Den
dc.identifier.issn1359-7345
dc.identifier.otherBibtex: urn:c61ec9fb61c61106d2ed0410ff80c7c4
dc.identifier.otherORCID: /0000-0002-8110-4535/work/59464839
dc.identifier.urihttps://hdl.handle.net/10023/18058
dc.descriptionThe authors are grateful for the support of The University of Edinburgh Chancellor Fellowship Scheme and State Key Laboratory for Membrane Separations, China (NTU-KL17-03).en
dc.description.abstractBy replacing Lewis acids with Brønsted acids as catalysts, continuous flow synthesis of hypercrosslinked polymers is achieved within 10% of the time required for a typical batch reaction. Compared with batch-synthesised polymers, the flow-produced materials take up 24% more CO2, precluding the need for lengthy reaction protocols to yield high-performance hypercrosslinked polymers for carbon capture.
dc.format.extent4
dc.format.extent2987715
dc.language.isoeng
dc.relation.ispartofChemical Communicationsen
dc.subjectQD Chemistryen
dc.subjectNDASen
dc.subject.lccQDen
dc.titleContinuous flow knitting of a triptycene hypercrosslinked polymeren
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doi10.1039/C9CC03731D
dc.description.statusPeer revieweden


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