硼与IV族元素化合物的键合研究。第四部分:用11B核共振研究三卤化硼的重分配平衡

M. Lappert, M. Litzow, J. Pedley, T. Spalding, H. Nöth
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引用次数: 5

摘要

在33.5℃的甲基环己烷和1,1-二氯乙烷溶剂中,用11B核磁共振光谱测定了三卤化硼的重分配平衡:1 / 3 BX3+ 1 / 3 BY3 + BX2Y和1 / 3 BX3+ 2 / 3 BY3 + BXY2;BCl3-BBr3系统的变温研究已经完成。熵变也从光谱数据中计算出来,与仅基于对称因素的计算结果相差不大。该反应仅稍微偏离热中性(<2 kcal mol-1),吸热性似乎随着X和y的电负性差异的增加而增加。在两种介质中没有检测到溶剂效应,并且在比较允许的范围内,与气相的情况没有明显的偏差。
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Bonding studies of compounds of boron and the group IV elements. Part IV. Redistribution equilibria among the boron trihalides by 11B nuclear resonance
Redistribution equilibria: ⅔BX3+⅓BY3⇌ BX2Y and ⅓BX3+⅔BY3⇌ BXY2 among all the boron trihalides have been examined by 11B n.m.r. spectroscopy in solvents methylcyclohexane and 1,1-dichloroethane at 33·5 °C; variable temperature studies have been completed for the BCl3–BBr3 systems. Entropy changes were also calculated from spectroscopic data and show tittle deviation from calculations based on symmetry factors alone. The reactions depart only slightly from thermoneutrality (<2 kcal mol–1) and endothermicity appears to increase with increasing disparity between the electronegativities of X and Y. There is no detectable solvent effect in the two media examined and, insofar as comparison permits, no significant deviation from the situation in the gas phase.
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