期刊
CHEMISTRY-A EUROPEAN JOURNAL
卷 16, 期 28, 页码 8508-8515出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201000127
关键词
boranes; calcium; dehydrocoupling; magnesium; structure elucidation
资金
- Nuffield Foundation
- Engineering and Physical Sciences Research Council [EP/E03117X/1] Funding Source: researchfish
- EPSRC [EP/E03117X/1] Funding Source: UKRI
Both homo- and heteroleptic alkyl and amide complexes of the Group 2 elements Mg and Ca are shown to be active for the catalytic de-hydrocoupling of Me2NH center dot BH3. Reactions of either magnesium dialkyls or the beta-diketiminate complex [HC{(Me)CN(Dipp)}(2)MgnBu] with four or two equivalents of Me2NHBH3, respectively, produce compounds containing the [H3BNMe2BH2Me2N](-) ion, which coordinates to the magnesium centers through Mg-N and Mg center dot center dot center dot HB interactions in both the solution and solid states. Thermolysis of these compounds at 60 degrees C produces the cyclic product [(H2BNMe2)2] and, it is proposed, magnesium hydrido species by an unprecedented delta-hydride elimination process. Calcium-based species, although less reactive than their magnesium-based counterparts, are found to engage in similar dehydrocoupling reactivity and to produce a similar distribution of products under thermally promoted catalytic conditions. A mechanism for these observations is presented that involves initial production and insertion of H2B=NMe2 into polarized M-N bonds as the major B-N bond-forming step. The efficacy of this insertion and subsequent beta- or delta-hydride elimination steps is proposed to be dependent upon the charge density and polarizing capability of the participating Group 2 center, providing a rationale for the observed differences in reactivity between magnesium and calcium.
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