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Synthesis of Known and Previously Inaccessible Poly(pyrazolyl)Borates under Mild Conditions

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Synthesis of Known and Previously Inaccessible Poly(pyrazolyl)Borates under Mild Conditions

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dc.contributor.author Melero, María M.
dc.contributor.author Klosek, Zuzanna
dc.contributor.author Ramírez de Arellano Sánchez, María del Carmen
dc.contributor.author Olmos Vergé, Andrea
dc.date.accessioned 2023-09-27T13:04:10Z
dc.date.available 2023-09-27T13:04:10Z
dc.date.issued 2023
dc.identifier.citation Melero, María M. Klosek, Zuzanna Ramírez de Arellano Sánchez, María del Carmen Olmos Vergé, Andrea 2023 Synthesis of Known and Previously Inaccessible Poly(pyrazolyl)Borates under Mild Conditions Journal of Organic Chemistry 88 13 9130 9135
dc.identifier.uri https://hdl.handle.net/10550/89667
dc.description.abstract Poly(pyrazolyl)borate ligands have been obtained through the reaction of highly reactive haloboranes with in situ formed pyrazolides under very mild conditions. This versatile synthetic method allows the selective synthesis of bis-, tris-, or tetrakis(pyrazolyl)borates. Furthermore, the method is compatible with the use of functional groups on the heterocyclic moieties of the poly(pyrazolyl)- borates that were not accessible to date. Strongly encumbered sodium and thallium(I) poly(pyrazolyl)borates with a reduced donating ability have been obtained for the first time.
dc.language.iso eng
dc.relation.ispartof Journal of Organic Chemistry, 2023, vol. 88, num. 13, p. 9130-9135
dc.subject Química orgànica
dc.title Synthesis of Known and Previously Inaccessible Poly(pyrazolyl)Borates under Mild Conditions
dc.type journal article
dc.date.updated 2023-09-27T13:04:10Z
dc.identifier.doi 10.1021/acs.joc.3c00761
dc.identifier.idgrec 161326
dc.rights.accessRights open access

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