Aerobic C–C and C–O bond formation reactions mediated by high-valent nickel species
dc.contributor.author
dc.date.accessioned
2020-06-17T07:41:41Z
dc.date.available
2020-06-17T07:41:41Z
dc.date.issued
2019-09-24
dc.identifier.issn
2041-6520
dc.identifier.uri
dc.description.abstract
Nickel complexes have been widely employed as catalysts in C–C and C–heteroatom bond formation reactions. While Ni(0), Ni(I), and Ni(II) intermediates are most relevant in these transformations, recently Ni(III) and Ni(IV) species have also been proposed to play a role in catalysis. Reported herein is the synthesis, detailed characterization, and reactivity of a series of Ni(II) and Ni(III) metallacycle complexes stabilized by tetradentate pyridinophane ligands with various N-substituents. Interestingly, while the oxidation of the Ni(II) complexes with various other oxidants led to exclusive C–C bond formation in very good yields, the use of O2 or H2O2 as oxidants led to formation of appreciable amounts of C–O bond formation products, especially for the Ni(II) complex supported by an asymmetric pyridinophane ligand containing one tosyl N-substituent. Moreover, cryo-ESI-MS studies support the formation of several high-valent Ni species as key intermediates in this uncommon Ni-mediated oxygenase-type chemistry
dc.format.mimetype
application/pdf
dc.language.iso
eng
dc.publisher
Royal Society of Chemistry (RSC)
dc.relation.isformatof
Reproducció digital del document publicat a: https://doi.org/10.1039/C9SC03758F
dc.relation.ispartof
Chemical Science, 2019,vol. 10, p. 10366-10372
dc.relation.ispartofseries
Articles publicats (D-Q)
dc.rights
Attribution-NonCommercial 4.0 International
dc.rights.uri
dc.subject
dc.title
Aerobic C–C and C–O bond formation reactions mediated by high-valent nickel species
dc.type
info:eu-repo/semantics/article
dc.rights.accessRights
info:eu-repo/semantics/openAccess
dc.type.version
info:eu-repo/semantics/publishedVersion
dc.identifier.doi
dc.identifier.idgrec
030363
dc.type.peerreviewed
peer-reviewed
dc.identifier.eissn
2041-6539