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Isolation, bonding and reactivity of a monomeric stibine oxide
In contrast to phosphine oxides and arsine oxides, which are common and exist as stable monomeric species featuring the corresponding pnictoryl functional group (Pn=O/Pn(+)–O(−); Pn = P, As), stibine oxides are generally polymeric, and the properties of the unperturbed stiboryl group (Sb=O/Sb(+)–O(−...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10159848/ https://www.ncbi.nlm.nih.gov/pubmed/36959510 http://dx.doi.org/10.1038/s41557-023-01160-x |
Sumario: | In contrast to phosphine oxides and arsine oxides, which are common and exist as stable monomeric species featuring the corresponding pnictoryl functional group (Pn=O/Pn(+)–O(−); Pn = P, As), stibine oxides are generally polymeric, and the properties of the unperturbed stiboryl group (Sb=O/Sb(+)–O(−)) remain unexplored. We now report the isolation of the monomeric stibine oxide, Dipp(3)SbO (where Dipp = 2,6-diisopropylphenyl). Spectroscopic, crystallographic and computational studies provide insight into the nature of the Sb=O/Sb(+)–O(−) bond. Moreover, isolation of Dipp(3)SbO allows the chemistry of the stiboryl group to be explored. Here we show that Dipp(3)SbO can act as a Brønsted base, a hydrogen-bond acceptor and a transition-metal ligand, in addition engaging in 1,2-addition, O-for-F(2) exchange and O-atom transfer. In all cases, the reactivity of Dipp(3)SbO differed from that of the lighter congeners Dipp(3)AsO and Dipp(3)PO. [Image: see text] |
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