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Photoisomerization dynamics study on cis-azobenzene derivative using ultraviolet-to-visible tunable femtosecond pulses

机译:紫外到可见光可调飞秒脉冲研究顺式偶氮苯衍生物的光异构动力学

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摘要

We performed the transient absorption measurement and the first rate equation (RE) analysis for cis isomer of 4-carboxy-2',6'-dimethylazobenzene to clarify the quantitative difference between the photoisomerization process and the thermal relaxation process from the S_1~C excited state. The RE analysis enabled us to determine the cis-to-trans photoisomerization rate per each pump pulse to be 3% under the condition of the 430 nm, 150 fs pump pulse with energy of 200 nJ. Moreover, the signal due to the yielded trans molecules appearing in the transient absorption was assigned from the following observed result: the transient absorbance change at the 380 nm probe mostly decreased within 300 fs after the 430 nm pulse pumping and then slowly decreased to zero, while the absorbance change at the 350 nm probe had a positive constant component in the over one picosecond time region. The RE analysis showed that this constant component is due to the yielded trans molecules, and its positive value is due to the fact that the absorption cross-section of the S_0~T -to- S_2~T transition in their trans molecules is larger than that of the S_0~C -to- S_2~C transition in the original cis molecules.
机译:我们对4-羧基-2',6'-二甲基偶氮苯的顺式异构体进行了瞬态吸收测量和一级速率方程(RE)分析,以阐明S_1〜C激发后光异构化过程和热弛豫过程之间的定量差异。州。 RE分析使我们能够确定在430 nm,150 fs泵浦脉冲和200 nJ能量的条件下,每个泵浦脉冲的顺式至反式光异构化率为3%。此外,根据以下观察到的结果,归因于瞬态吸收中出现的反式分子的产生所产生的信号:在430 nm脉冲泵浦后的300 fs内,380 nm探针的瞬态吸收率变化大部分减小,然后缓慢减小至零,而350 nm探针的吸光度变化在超过1皮秒的时间范围内具有正常数分量。 RE分析表明,该恒定组分是由产生的反式分子引起的,而其正值是由于其反式分子中S_0〜T至S_2〜T跃迁的吸收截面大于原始顺式分子中S_0〜C到S_2〜C的跃迁

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  • 来源
    《Applied Surface Science》 |2009年第24期|9864-9868|共5页
  • 作者单位

    Department of Applied Physics, Graduate School of Engineering, Hokkaido University and Core Research for Evolution Science and Technology (CREST)Japan Science and Technology Agency (JST), Kita-13, Nishi-8, Kita-ku, Sapporo 060-8628, Japan;

    Department of Applied Physics, Graduate School of Engineering, Hokkaido University and Core Research for Evolution Science and Technology (CREST)Japan Science and Technology Agency (JST), Kita-13, Nishi-8, Kita-ku, Sapporo 060-8628, Japan;

    Department of Applied Physics, Graduate School of Engineering, Hokkaido University and Core Research for Evolution Science and Technology (CREST)Japan Science and Technology Agency (JST), Kita-13, Nishi-8, Kita-ku, Sapporo 060-8628, Japan;

    Department of Applied Physics, Graduate School of Engineering, Hokkaido University and Core Research for Evolution Science and Technology (CREST)Japan Science and Technology Agency (JST), Kita-13, Nishi-8, Kita-ku, Sapporo 060-8628, Japan;

    Department of Molecular Design and Engineering, Graduate School of Engineering, Nagoya University and Core Research for Evolution Science and Technology (CREST), Japan Science and Technology Agency (JST), Nagoya 464-8603, Japan;

    Department of Molecular Design and Engineering, Graduate School of Engineering, Nagoya University and Core Research for Evolution Science and Technology (CREST), Japan Science and Technology Agency (JST), Nagoya 464-8603, Japan;

    Department of Applied Physics, Graduate School of Engineering, Hokkaido University and Core Research for Evolution Science and Technology (CREST)Japan Science and Technology Agency (JST), Kita-13, Nishi-8, Kita-ku, Sapporo 060-8628, Japan;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    ultrafast photoisomerization dynamics; azobenzene derivative; transient absorption measurement; rate equation analysis;

    机译:超快光异构化动力学;偶氮苯衍生物;瞬态吸收测量;速率方程分析;
  • 入库时间 2022-08-18 03:07:51

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