首页> 外文期刊>Journal of Photochemistry and Photobiology, A. Chemistry >Picosecond time-resolved luminescence of Pr(III) complexes: Intramolecular excitation energy transfer from ligand to Pr(III)
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Picosecond time-resolved luminescence of Pr(III) complexes: Intramolecular excitation energy transfer from ligand to Pr(III)

机译:皮秒时间分辨的Pr(III)配合物发光:分子内激发能从配体转移到Pr(III)

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摘要

The intramolecular excitation energy transfer from the fluorophore ligand (phens) to Pr(III) in the complexes on the basis of the picosecond time-resolved luminescence spectra is discussed. These complexes exhibit sequentially multiplex emissions from the energy levels on the ligand as (1)pi pi(1)* in the UV region, and from those on Pr(III) as ff in the visible region. From the decay curve analysis of these emissions, the intramolecular energy transfer pathway was clarified quantitatively following the spin-selection rule. The rate constants of energy transfer from the ligand to Pr(III) were estimated, from the (1)pi pi(1)* of phen to the I-1(6) state of Pr(III) via the triplet state. This mechanism can be applied to control the emission properties of Pr(III) complexes by changing the emissive f-levels due to ligand variations. (c) 2005 Published by Elsevier B.V.
机译:讨论了基于皮秒时间分辨的发光光谱,从配合物中的荧光团配体(phens)到Pr(III)的分子内激发能转移。这些配合物在紫外区域的配位能级依次为(1)pi pi(1)*,在可见光区域的pr(III)级为ff。从这些排放物的衰减曲线分析中,遵循自旋选择规则定量阐明了分子内能量转移途径。估计了从配体到Pr(III)的能量转移速率常数,从phen的(1)pi pi(1)*经由三重态到Pr(III)的I-1(6)状态。通过改变由于配体变化而引起的f-能级,该机制可用于控制Pr(III)配合物的发射性质。 (c)2005年由Elsevier B.V.

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