Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/84480
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dc.contributor.authorBurgun, A.-
dc.contributor.authorCrees, R.-
dc.contributor.authorCole, M.-
dc.contributor.authorDoonan, C.-
dc.contributor.authorSumby, C.-
dc.date.issued2014-
dc.identifier.citationChemical Communications, 2014; 50(79):11760-11763-
dc.identifier.issn1364-548X-
dc.identifier.issn1364-548X-
dc.identifier.urihttp://hdl.handle.net/2440/84480-
dc.descriptionIncludes supplementary information-
dc.description.abstractA new MOF, [Zn4O{Cu(L)2}2] (1), with a 4-fold interpenetrated 3D diamondoid structure was synthesised from in situ generated [Cu(L)2] NHC linkers. MOF 1 possesses tetrahedral Zn4O nodes, which are unusually coordinated by four pairs of carboxylates from four [Cu(L)2] linkers, and 14 A 1-D pore channels lined with [Cu(L)2] moieties that catalyse the hydroboration of CO2.-
dc.description.statementofresponsibilityAlexandre Burgun, Rachel S. Crees, Marcus L. Cole, Christian J. Doonan and Christopher J. Sumby-
dc.language.isoen-
dc.publisherRoyal Society of Chemistry-
dc.rightsThis journal is © The Royal Society of Chemistry 2014-
dc.titleA 3-D diamondoid MOF catalyst based on in situ generated [Cu(L)2] N-heterocyclic carbene (NHC) linkers: hydroboration of CO₂-
dc.title.alternativeA 3-D diamondoid MOF catalyst based on in situ generated [Cu(L)2] N-heterocyclic carbene (NHC) linkers: hydroboration of CO(2)-
dc.typeJournal article-
dc.identifier.doi10.1039/C4CC04761C-
dc.relation.granthttp://purl.org/au-research/grants/arc/FT100100400-
dc.relation.granthttp://purl.org/au-research/grants/arc/FT0991910-
pubs.publication-statusPublished-
dc.identifier.orcidSumby, C. [0000-0002-9713-9599]-
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Chemistry and Physics publications

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