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首页> 外文期刊>Bulletin of the Korean Chemical Society >Photophysical Model of 10-Hydroxybenzo[h]quinoline: Internal Conversion and Excited State Intramolecular Proton Transfer
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Photophysical Model of 10-Hydroxybenzo[h]quinoline: Internal Conversion and Excited State Intramolecular Proton Transfer

机译:10-羟基苯并[h]喹啉的光物理模型:内部转换和激发态分子内质子转移

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Photophysics of 10-hydroxybenzo[/7]quinoline (HBQ) has been in controversy, in particular, on the nature of the electronic states before and after the excited state intramolecular proton transfer (ESIPT), even though the dynamics and mechanism of the ESDPT have been well established. We report highly time resolved fluorescence spectra over the full emission frequency regions of the enol and keto isomers and the anisotropy in time domain to determine the accurate rates of the population decay, spectral relaxation and anisotropy decay of the keto isomer. We have shown that the-300 fs component observed frequently in ESIPT dynamics arises from the S2→ S1 internal conversion in the reaction product keto isomer and that the ESIPT occurs from the enol isomer in S1 state to the keto isomer in S2 state.
机译:10-羟基苯并[/ 7]喹啉(HBQ)的光物理性质一直存在争议,特别是关于激发态分子内质子转移(ESIPT)前后的电子态性质,即使ESDPT的动力学和机理也是如此。已经建立。我们报告了在烯醇和酮异构体的整个发射频率区域和时域各向异性的高度时间分辨的荧光光谱,以确定了酮异构体的种群衰减,光谱弛豫和各向异性衰减的准确率。我们已经表明,在ESIPT动力学中经常观察到的-300 fs组分是由反应产物酮异构体中的S2→S1内部转化引起的,并且ESIPT发生于从S1状态的烯醇异构体到S2状态的酮异构体。

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