化学
加合物
脱氢
阳离子聚合
药物化学
盐变质反应
吡啶
碘甲烷
复分解
高分子化学
无机化学
有机化学
聚合
催化作用
聚合物
作者
Chen Zhang,Xin Jiang,Yi Jing,Na Zhang,Peng Wang,Hongju Wang,Kai Jiang,Ximeng Chen,Xuenian Chen
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2024-05-28
卷期号:63 (23): 10519-10526
被引量:1
标识
DOI:10.1021/acs.inorgchem.4c00772
摘要
The BCN-heterocyclic B–N chain compounds, the sodium and potassium salts of 3 and 4 anions (Na3, Na4, and K4), were synthesized by reactions of ethane 1,2-diamineborane (BH3NH2CH2CH2NH2BH3, 1) and propane 1,2-diamineborane (BH3NH2CH2CH2CH2NH2BH3, 2) with MH (M = Na and K). Then, the neutral B–N chain compounds 5 and 6 were prepared with dehydrogenation of [NH4]3 and [NH4]4, formed by metathesis reactions of Na3 and Na4 with NH4Cl or NH4SCN, respectively. Compounds 7 and 8, analog 5, were also prepared using pyridine and 4-methoxypyridine instead of NH3 in 5. These synthesized compounds were characterized spectroscopically, and the singe-crystal structures of the Na3·18-crown-6 and K4·18-crown-6 adducts were determined. Furthermore, the reactions of Na3 and Na4 with cationic B–N chain compounds, [NH3BH2NH3]Cl and [NH3BH2NH2BH2NH3]Cl, could not form longer BCN-heterocyclic B–N chain. The solubility of metal hydrides, the ability for proton abstracting, the basicity of Lewis bases, and the chelate effect may influence these reactions even though the reaction mechanism is not fully understood.
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