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首页> 外文期刊>Zeitschrift fur Naturforschung, B. A Journal of Chemical Sciences >1,2-Hydroboration and 1,1-Carboboration of Alkynyl(ferrocenyl)vinylsilanes. Novel Siloles
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1,2-Hydroboration and 1,1-Carboboration of Alkynyl(ferrocenyl)vinylsilanes. Novel Siloles

机译:炔基(二茂铁基)乙烯基硅烷的1,2-氢硼化和1,1-碳硼化。新型筒仓

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摘要

Alkynyl(ferrocenyl)vinylsilanes containing up to three alkynyl units were prepared and treated with 9-borabicyclo[3.3.1]nonane (9-BBN). All reactions proceeded in the beginning by regioselective 1,2-hydroboration of the vinyl group, with boron attached to the terminal carbon. This was followed by intra-molecular 1,1-carboboration, leading to fused silacarbacycles, depending on the number of CC bonds. Thus, new siloles and even fused siloles became available. The solution-state structures were revealed by multinuclear NMR techniques (H-1, B-11, C-13, (SiNMR)-Si-29), xcomplemented by calculated single-molecule structures and calculated NMR parameters at the B3LYP/6-311+G(d,p) level of theory. In one case, the solid-state structure of a bicyclic derivative was determined.
机译:制备含有最多三个炔基单元的炔基(二茂铁基)乙烯基硅烷,并用9-硼环[3.3.1]壬烷(9-BBN)处理。所有的反应都是通过乙烯基的区域选择性1,2-氢硼化反应开始的,其中硼连接到末端碳上。随后,根据CC键的数量,分子内的1,1-碳化作用会导致熔融的硅碳环化合物。因此,可以使用新的筒仓甚至是熔融筒仓。通过多核NMR技术(H-1,B-11,C-13,(SiNMR)-Si-29)揭示了溶液状态结构,并通过计算的单分子结构和在B3LYP / 6-处的NMR参数进行了补充。 311 + G(d,p)的理论水平。在一种情况下,确定了双环衍生物的固态结构。

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