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dc.contributor.authorZhu, Jiayun
dc.contributor.authorMoreno, Immaculada
dc.contributor.authorQuinn, Peter
dc.contributor.authorYufit, Dmitry S.
dc.contributor.authorSong, Lijuan
dc.contributor.authorYoung, Claire M.
dc.contributor.authorDuan, Zhuan
dc.contributor.authorTyler, Andrew R.
dc.contributor.authorWaddell, Paul G.
dc.contributor.authorHall, Michael J.
dc.contributor.authorProbert, Michael R.
dc.contributor.authorSmith, Andrew D.
dc.contributor.authorO'Donoghue, AnnMarie C.
dc.date.accessioned2022-03-02T10:30:03Z
dc.date.available2022-03-02T10:30:03Z
dc.date.issued2022-03-18
dc.identifier.citationZhu , J , Moreno , I , Quinn , P , Yufit , D S , Song , L , Young , C M , Duan , Z , Tyler , A R , Waddell , P G , Hall , M J , Probert , M R , Smith , A D & O'Donoghue , A C 2022 , ' The role of the fused ring in bicyclic triazolium organocatalysts : kinetic, X-ray and DFT insights ' , The Journal of Organic Chemistry , vol. 87 , no. 6 , pp. 4241-4253 . https://doi.org/10.1021/acs.joc.1c03073en
dc.identifier.issn0022-3263
dc.identifier.otherPURE: 277902903
dc.identifier.otherPURE UUID: bd5d7753-0614-4edb-9a76-8c4c182a7a7b
dc.identifier.otherScopus: 85125960046
dc.identifier.otherWOS: 000776255900032
dc.identifier.otherORCID: /0000-0002-2104-7313/work/117211348
dc.identifier.urihttps://hdl.handle.net/10023/24973
dc.descriptionAuthors thank the EPSRC (JZ and CMY, EP/S020713/1; PQ, EP/M506321/1), ZD (CSC St Andrews PhD studentship), Universidad de Castilla-La Mancha and the European Regional Development Fund (IM) and the BBSRC (MJH, MRP and ART, BB/L013754/1) for funding.en
dc.description.abstractBicyclictriazolium scaffolds are widely employed in N-heterocycliccarbene (NHC) organocatalysis. Whilst the incorporation of a fused ring wasinitially for synthetic utility in accessing chiral, modular triazolyl scaffolds,recent results highlight the potential for impact upon reaction outcome with underpinningorigins unclear.  The common first stepto all triazolium-catalyzed transformations is C(3)-H deprotonation to form thetriazolylidene NHC.  Herein, we report ananalysis of the impact of size of the fused (5-, 6- and 7-membered, n=1, 2 and3 respectively) ring on the C(3) proton transfer reactions of a series of bicyclictriazolium salts. Rate constants for the deuteroxide-catalyzed C(3)-H/D-exchangeof triazolium salts, kDO, weresignificantly influenced by the size of the adjacent fused ring, with the kineticacidity trend, or protofugalities, following the order: kDO (n=1) > kDO(n=2) ≈ kDO (n=3). Detailed analyses of X-raydiffraction (XRD) data for 20triazolium salts (including 16 new structures), and of computational data forthe corresponding triazolylidene NHCs, provide insight on structural effects ofalteration of fused ring size. In particular, changes in internal triazolyl NCNangle and positioning of the most proximal CH2 with variation infused ring size are proposed to explain the experimental protofugality order.
dc.language.isoeng
dc.relation.ispartofThe Journal of Organic Chemistryen
dc.rightsCopyright © 2022 The Author(s). This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.en
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.titleThe role of the fused ring in bicyclic triazolium organocatalysts : kinetic, X-ray and DFT insightsen
dc.typeJournal articleen
dc.contributor.sponsorEPSRCen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.identifier.doihttps://doi.org/10.1021/acs.joc.1c03073
dc.description.statusPeer revieweden
dc.identifier.grantnumberEP/S019359en


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