The role of free space in photochemical reactions in crystals at high pressure - the case of 9-methylanthracene.

Julia Bąkowicz, I. Turowska-Tyrk
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Abstract

The influence of pressure on the course of [4+4] photodimerization in crystals of 9-methylanthracene is presented. The studies were performed at 0.1 and 0.4 GPa. As a result of the reaction at high pressure, crystals of the pure product were obtained, which allowed for monitoring of the reaction until its completion. The initial increase in the unit-cell volume caused by the reaction under ambient conditions was reduced at high pressure due to the decrease in the void volume. Despite the smaller size of the void volume at high pressure, dimer molecules formed during the reaction changed the orientation of the monomer molecules in the crystal structure. The size of the voids above the terminal rings of the monomers correlates with the position of the terminal rings in the dimer. The reaction rate increased at high pressure, indicating that the decrease in the distance between adjacent monomers caused by pressure dominates over the decrease in the void volume. This distance is statistically constant as the reaction progresses, contrary to the reaction at ambient pressure.
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自由空间在高压晶体光化学反应中的作用——以9-甲基蒽为例。
研究了压力对9-甲基蒽晶体中[4+4]光二聚化过程的影响。研究分别在0.1和0.4 GPa下进行。在高压下反应的结果是,获得了纯产物的晶体,这使得可以监测反应直到反应完成。在高压条件下,由于空隙体积的减小,初始反应引起的单胞体积的增大减小了。尽管高压下的孔隙体积较小,但反应过程中形成的二聚体分子改变了单体分子在晶体结构中的取向。单体末端环上方空隙的大小与末端环在二聚体中的位置有关。在高压下反应速率增加,说明压力引起的相邻单体之间距离的减小大于空隙体积的减小。与环境压力下的反应相反,随着反应的进行,这个距离在统计上是恒定的。
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