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dc.contributor.authorVeinot, Alex
dc.contributor.authorAl-Rashed, Abrar
dc.contributor.authorPadmos, J. Daniel
dc.contributor.authorSingh, Ishwar
dc.contributor.authorLee, Dianne S.
dc.contributor.authorNarouz, Mina R.
dc.contributor.authorLummis, Paul A.
dc.contributor.authorBaddeley, Christopher J.
dc.contributor.authorCrudden, Cathleen Marie
dc.contributor.authorHorton, J. Hugh
dc.date.accessioned2021-08-06T23:39:22Z
dc.date.available2021-08-06T23:39:22Z
dc.date.issued2020-08-07
dc.identifier268707567
dc.identifierd3c26e6c-91ba-483f-afa1-4e0eab755443
dc.identifier85089099323
dc.identifier000556302100001
dc.identifier.citationVeinot , A , Al-Rashed , A , Padmos , J D , Singh , I , Lee , D S , Narouz , M R , Lummis , P A , Baddeley , C J , Crudden , C M & Horton , J H 2020 , ' N-heterocyclic carbenes reduce and functionalize copper oxide surfaces in one pot ' , Chemistry - A European Journal , vol. Early View . https://doi.org/10.1002/chem.202002308en
dc.identifier.issn0947-6539
dc.identifier.otherRIS: urn:51B21FBB35A3BC030D8BAB0ED03A4876
dc.identifier.otherORCID: /0000-0001-9750-6494/work/78891559
dc.identifier.urihttps://hdl.handle.net/10023/23736
dc.descriptionThe Natural Sciences and Engineering Research Council of Canada (NSERC) and the Canada Foundation for Innovation (CFI) are thanked for financial support of this work in terms of operating and equipment grants to CMC and JHH. AJV and MRN thank the Ontario government for OGS fellowships. AJV thanks NSERC for a Vanier Scholarship and also the Walter C. Sumner foundation for additional scholarship support.en
dc.description.abstractBenzimidazolium hydrogen carbonate salts have been shown to act as N-heterocyclic carbene precursors which can remove oxide from copper oxide surfaces and functionalize the resulting metallic surfaces in a single step. Both the surfaces and the etching products are fully characterized by spectroscopic methods. Analysis of surfaces before and after NHC treatment by X-ray photoelectron spectroscopy demonstrates the complete removal of copper(II) oxide. Using 13C-labelling, we determine that the products of this transformation include a cyclic urea, a ring-opened formamide and a bis-carbene copper(I) complex. These results illustrate the potential of NHCs to functionalize a much broader class of metals, including those prone to oxide treatment, greatly facilitating the preparation of NHC-based films on metals other than gold.
dc.format.extent1362765
dc.language.isoeng
dc.relation.ispartofChemistry - A European Journalen
dc.subjectN-Heterocyclic carbeneen
dc.subjectCopper oxideen
dc.subjectReductionen
dc.subjectSelf assembled monolayeren
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.titleN-heterocyclic carbenes reduce and functionalize copper oxide surfaces in one poten
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doi10.1002/chem.202002308
dc.description.statusPeer revieweden
dc.date.embargoedUntil2021-08-07


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