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The photoisomerization of aqueous ICN studied by subbicosecond transient absorption spectroscopy

机译:亚亚秒级瞬态吸收光谱研究含水ICN的光异构化

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The photolysis of aqueous ICN is studied by transient absorption spectroscopy covering the spectral range from 227 to 714 nm with 0.5 ps time resolution. The experimental data show that when ICN (aq) is photolyzed at 266 nm, it dissociates into I and CN and both the I(~2P_(3/2)) and I(~2P_(1/2)) channels are populated. Approximately half the fragments escape the solvent cage while the remainder recombines within the solvent cage during the first picosecond. The majority of the recombinations form ICN while only a minor fraction produces the metastable INC isomer. INC and ICN relax to the vibrational ground state within 1 ps in good agreement with theoretical estimates based on the golden rule formalism as well as molecular dynamics simulations. Diffusive recombination involving fragments that have escaped the solvent cage further reduces the quantum yield of I and CN to 10% during the following 100 ps. This recombination produces exclusively ICN.
机译:通过瞬态吸收光谱研究了ICN水溶液的光解,该光谱涵盖了从227到714 nm的光谱范围,时间分辨率为0.5 ps。实验数据表明,当ICN(aq)在266 nm处光解时,它解离为I和CN,并且同时填充了I(〜2P_(3/2))和I(〜2P_(1/2))通道。在第一个皮秒内,大约一半的碎片逸出了溶剂笼,其余的则在溶剂笼内重组。大部分重组形成ICN,而只有一小部分产生亚稳的INC异构体。 INC和ICN放松到1 ps内的振动基态,这与基于黄金法则形式主义和分子动力学模拟的理论估计非常吻合。在随后的100 ps期间,涉及已逃离溶剂笼的片段的扩散重组进一步将I和CN的量子产率降低至10%。该重组仅产生ICN。

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