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首页> 外文期刊>Journal of Photochemistry and Photobiology, A. Chemistry >Molecular Stark-effect spectroscopy of Prodan and Laurdan in different solvents and electric dipole moments in their equilibrated ground and Franck-Condon excited state
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Molecular Stark-effect spectroscopy of Prodan and Laurdan in different solvents and electric dipole moments in their equilibrated ground and Franck-Condon excited state

机译:Prodan和Laurdan在平衡基态和Franck-Condon激发态下在不同溶剂和电偶极矩中的分子斯塔克效应光谱

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摘要

he results from electrooptical absorption measurements (EDAM) on the ground and excited Franck-Condon state dipole moments of Prodan and Laurdan in 1,4-dioxane and cyclohexane are presented. The ground and excited Franck-Condon state electric dipole moments as well as the respective transition moment of both probes are parallel. The electric dipole moments of Prodan and Laurdan in the ground state in cyclohexane and 1,4-dioxane have values within the range (15.7-16.5) x 10(-30) C m. On optical excitation the dipole moments increase by (42.1-49.5) x 10(-30) C m. The obtained results are compared with the values of the dipole moments of Prodan and Laurdan determined by other methods. (c) 2006 Elsevier B.V. All rights reserved.
机译:他从地面上的电光吸收测量(EDAM)得到了结果,并给出了Prodan和Laurdan在1,4-二恶烷和环己烷中的Franck-Condon态激发偶极矩。基波和激发态的弗兰克-康登状态电偶极矩以及两个探头各自的跃迁矩是平行的。 Prodan和Laurdan在环己烷和1,4-二恶烷中处于基态的电偶极矩值在(15.7-16.5)x 10(-30)C m范围内。在光激发下,偶极矩增加(42.1-49.5)x 10(-30)C m。将获得的结果与通过其他方法确定的Prodan和Laurdan的偶极矩值进行比较。 (c)2006 Elsevier B.V.保留所有权利。

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