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dc.contributor.authorKumar, Amit
dc.contributor.authorPriest, Isobel K.
dc.contributor.authorHooper, Thomas N.
dc.contributor.authorWeller, Andrew S.
dc.date.accessioned2020-11-04T14:30:01Z
dc.date.available2020-11-04T14:30:01Z
dc.date.issued2016-04-14
dc.identifier.citationKumar , A , Priest , I K , Hooper , T N & Weller , A S 2016 , ' Variable coordination modes and catalytic dehydrogenation of B -phenyl amine–boranes ' , Dalton Transactions , vol. 45 , no. 14 , pp. 6183-6195 . https://doi.org/10.1039/c6dt00197aen
dc.identifier.issn1477-9226
dc.identifier.otherPURE: 265466022
dc.identifier.otherPURE UUID: 1885fe1b-5867-421b-adf1-9ae98f6341d1
dc.identifier.otherScopus: 84963729611
dc.identifier.otherORCID: /0000-0002-8175-8221/work/68281839
dc.identifier.urihttp://hdl.handle.net/10023/20898
dc.descriptionThe EPSRC (EP/J02127X) and the Rhodes Trust for funding.en
dc.description.abstractThe chemistry of N-substituted amine–boranes and their reactivity towards transition metal centres is well established but the chemistry of B-substituted amine–boranes is not. Here we present the coordination chemistry of H2PhB·NMe3 towards a range of Rh(I) fragments with different P–Rh–P ligand bite angles, {Rh(PiPr3)2}+, {Rh(PiBu3)2}+, {Rh(iPr2P(CH2)3PiPr2)}+, {Rh(Ph2P(CH2)nPPh2)}+ (n = 3, 5), as characterised by NMR spectroscopy and single-crystal X-ray diffraction. This reveals a difference in the coordination mode of the amine–borane, with large bite angle fragments favouring η2-coordination through a sigma-interaction with BH2, whereas fragments with small bite angles favour η6-coordination through the aryl group of the amine–borane. The catalytic dehydrocoupling of H2PhB·NMe2H is also explored, with the aminoborane HPhBNMe2 found to be the sole dehydrogenation product. Stoichiometric reactivity with H2PhB·NMe2H again showed small bite angle fragments to prefer η6-aryl coordination, while the larger bite angle {Rh(PiPr3)2}+ gave rapid dehydrogenation to form a mixture of the Rh(III) dihydride [Rh(PiPr3)2(H)2(η2-H2PhB·NMe2H)][BArF4] and the low coordinate aminoboryl complex [Rh(PiPr3)2(H)(BPhNMe2)][BArF4]. These results suggest that precatalysts which η6-bind arenes strongly should be avoided for the dehydrocoupling of amine–boranes bearing aryl substituents
dc.language.isoeng
dc.relation.ispartofDalton Transactionsen
dc.rightsCopyright © 2016 The Author(s). Open Access Article. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.en
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.titleVariable coordination modes and catalytic dehydrogenation of B-phenyl amine–boranesen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews.School of Chemistryen
dc.identifier.doihttps://doi.org/10.1039/c6dt00197a
dc.description.statusPeer revieweden


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