自由基阴离子的反应。第十部分:偶氮苯、萘-1-偶氮苯、1,1′-偶氮萘和2,2′-偶氮萘自由基阴离子的电子自旋共振研究,包括紧离子对-松离子对平衡的测量

A. G. Evans, J. Evans, P. J. Emes, C. L. James, P. J. Pomery
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引用次数: 3

摘要

用e.s.r法测定了四氢呋喃中偶氮苯、萘-1-偶氮苯、1,1′-偶氮萘和2,2′-偶氮萘在不同温度下的自由基-阴离子浓度,测定了温度对歧化平衡的影响,并测定了这些歧化平衡的平衡常数ΔH°值和ΔS°值。得到并分析了这些自由基阴离子的高分辨e.s.r.谱,并与简单的Huckel和McLachlan理论处理得到的分裂常数进行了比较。测定了偶氮苯和萘-1-偶氮苯金属分裂的温度依赖性。除钠外,在所有情况下,几乎没有观察到温度效应。然而,在钠的情况下,发现了金属分裂和超细分裂线宽度的明显温度依赖性,这已经被解释为紧离子对-松散离子对平衡。这些平衡的平衡常数,ΔH°值,ΔS°值,速率常数,ΔH‡和ΔS‡值已经确定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reactions of radical anions. Part X. Electron spin resonance study of the radical anions of azobenzene, naphthalene-1-azobenzene, 1,1′-azonaphthalene, and 2,2′-azonaphthalene including the measurements of tight ion-pair–loose ion-pair equilibria
The effect of temperature on the disproportionation equilibria of the radical anions of azobenzene, naphthalene-1-azobenzene, 1,1′-azonaphthalene, and 2,2′-azonaphthalene in tetrahydrofuran with various alkali metals as gegenions has been determined by measurement of the radical-anion concentration at different temperatures by e.s.r. Equilibrium constants, ΔH° values, and ΔS° values have been determined for these disproportionation equilibria.Well resolved e.s.r. spectra of these radical anions were obtained and analysed and the analysis was compared with the splitting constants obtained from simple Huckel and McLachlan theoretical treatment. The temperature dependence of the metal splittings were measured for azobenzene and naphthalene-1-azobenzene. In all cases except sodium, practically no temperature effect was observed. In the case of sodium, however, a marked temperature dependence of metal splitting and hyperfine splitting line widths were found which have been interpreted in terms of tight ion-pair–loose ion-pair equilibria. Equilibrium constants, ΔH° values, ΔS° values, rate constants, ΔH‡, and ΔS‡ values for these equilibria have been determined.
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