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Reactivity of a Platinum Iminoboryl Complex toward Lewis and Bronsted Acids

机译:铂氨基硼烷基络合物对路易斯酸和布朗斯台德酸的反应性

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Recently, research in our laboratory focused on the interaction of bromoboranes with [Pt(PCy_3)_2] (1), leading to the isolation of a number of unusual platinum complexes, such as a cationic T-shaped platinum boryl species, a cationic base-stabilized borylene complex, and a cationic terminal borylene compound. Furthermore, we recently reported the straightforward formation and full characterization of the iminoboryl complex trans-[(PCy_3)_2Pt(B≡NSiMe_3)-(Br)] (2), obtained upon B—Br bond oxidative addition of (Me_3-Si)_2NBBr_2 to 1 and subsequent Me_3SiBr elimination at room temperature. Iminoboranes, RB≡NR', are highly reactive compounds by virtue of their polar, unsaturated nature. As a result, in the absence of sterically encumbering substituents on either side of the B≡N triple bond, these species are prone to cyclooligomer-ization or polymerization. Differently from typical iminoboranes, 2 displays a remarkable stability against oligomerization.
机译:最近,我们实验室的研究集中在溴硼烷与[Pt(PCy_3)_2](1)的相互作用上,从而导致分离出许多不同寻常的铂络合物,例如阳离子T形铂硼基物种,阳离子碱-稳定的亚芳基配合物和阳离子末端亚芳基化合物。此外,我们最近报道了通过B-Br键氧化添加(Me_3-Si)获得的亚氨基硼烷基配合物反式[[PCy_3)_2Pt(B≡NSiMe_3)-(Br)](2)的直接形成和完整表征。 _2NBBr_2为1,然后在室温下消除Me_3SiBr。氨基硼烷RB≡NR'由于其极性,不饱和性质而成为高反应性化合物。结果,在B≡N三键的任一侧都没有在空间上占优势的取代基,这些物质易于发生环低聚或聚合。与典型的亚氨基硼烷不同,2显示出显着的抗低聚稳定性。

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