Tokunaga Ayako, Mutoh Katsuya, Hasegawa Takeshi, Abe Jiro
Department of Chemistry , School of Science and Engineering, Aoyama Gakuin University , 5-10-1 Fuchinobe , Chuo-ku, Sagamihara , Kanagawa 252-5258 , Japan.
Laboratory of Chemistry for Functionalized Surfaces, Division of Environmental Chemistry, Institute for Chemical Research , Kyoto University , Gokasho, Uji , Kyoto 611-0011 , Japan.
J Phys Chem Lett. 2018 Apr 19;9(8):1833-1837. doi: 10.1021/acs.jpclett.8b00916. Epub 2018 Mar 29.
We report here a kinetic study on the thermal equilibrium process between the biradical form and the quinoidal form starting from the singlet biradical form alone. A photochromic phenoxyl-imidazolyl radical complex repeatedly generates biradical species upon UV light irradiation, and the following thermal equilibrium process responsible for valence isomerization from the open-shell singlet biradical to the closed-shell quinoidal form is observed in the microsecond time region. The thermodynamic parameters for the equilibrium process were determined for the first time by nanosecond laser flash photolysis. We also found that visible-light excitation to the equilibrium state causes valence photoisomerization from the quinoidal to the biradical form, which returns thermally to the quinoidal form.
我们在此报告一项动力学研究,该研究针对仅从单重态双自由基形式开始的双自由基形式与醌型形式之间的热平衡过程。一种光致变色苯氧基 - 咪唑基自由基络合物在紫外光照射下反复产生双自由基物种,并且在微秒时间范围内观察到随后负责从开壳单重态双自由基到闭壳醌型形式的价异构化的热平衡过程。首次通过纳秒激光闪光光解确定了平衡过程的热力学参数。我们还发现,对平衡态的可见光激发会导致从醌型到双自由基形式的价光异构化,其会热返回到醌型形式。