Synthesis, structure, and reaction of tricoordinate stibine and tetracoordinate stiboranide |
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Authors: | Xin-Dong Jiang Yohsuke Yamamoto |
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Affiliation: | a The Key Laboratory for Special Functional Materials Ministry of Education, Henan University, Kaifeng, Henan 475-004, China b Department of Chemistry, Graduate School of Science, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima 739-8526, Japan |
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Abstract: | Tricoordinate stibine 1 and tetracoordinate stiboranide 2a were synthesized by utilizing SbCl3. The structure of 2a was confirmed by X-ray analysis. The interconversion between 1 and 2 could be achieved by BrNEt4 and NaH or BuLi. The pentacoordinate apicophilic stiborane 6 was prepared from 1. Due to steric repulsion between the TIP group and the aromatic ring, the C1-Sb-C2 angle of 6b was narrowed by 4.4° compared to that of 6a by X-ray analysis. |
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Keywords: | Berry pseudorotation Apicophilic Stiboranide Stiborane Isomerization |
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