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Differential scanning calorimetry in studies of solid-state reactions in photochromic materials

机译:差示扫描量热法研究光致变色材料中的固态反应

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Differential scanning calorimetry (DSC) was employed to study the kinetics of reverse thermally driven reactions in polycrystalline samples of three photochromic compounds. Results obtained on two dihydropyridine derivatives were critically re-examined and compared with results of the experiments performed with an acridizinium salt. Heat flow curves, measured on samples previously irradiated with UV, exhibited broad exothermic anomalies at elevated temperatures (above ca. 320 K for dihydropyridines and above ca. 490 K for the acridizinium salt), observed only once after irradiation and attributed to bleaching reactions. The activation energies of bleaching reactions in the dihydropyridine derivatives, determined from fractional heating experiments, amount to ca. 90-170 kJ/mol. Exact determination of the distribution of activation energies proved difficult due to uncertainties with a proper setting of baselines.
机译:差示扫描量热法(DSC)用于研究三种光致变色化合物的多晶样品中反向热驱动反应的动力学。严格地重新检查了在两种二氢吡啶衍生物上获得的结果,并与用cri啶鎓盐进行的实验结果进行了比较。在先前用紫外线照射过的样品上测得的热流曲线在升高的温度下表现出广泛的放热异常(二氢吡啶大约在320 K以上,a啶鎓盐大约在490 K以上),仅在辐射后才观察到一次,这归因于漂白反应。由分步加热实验确定的二氢吡啶衍生物中的漂白反应的活化能约为。 90-170 kJ /摩尔。由于基准线的正确设置存在不确定性,因此很难准确确定活化能的分布。

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