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应用于飞秒瞬态吸收光谱分析超快过程的软硬混合建模:水杨醛苯胺光致变色的研究

Hybrid hard- and soft-modelling applied to analyze ultrafast processes by femtosecond transient absorption spectroscopy: study of the photochromism of salicylidene anilines.

作者信息

Ruckebusch C, Sliwa M, Réhault J, Naumov P, Huvenne J P, Buntinx G

机构信息

Laboratoire de Spectrochimie Infrarouge et Raman (LASIR CNRS), Centre d'Etudes et de Recherches Lasers et Applications, Université de Lille1, bât C5, 59655 Villeneuve d'Ascq, France.

出版信息

Anal Chim Acta. 2009 May 29;642(1-2):228-34. doi: 10.1016/j.aca.2008.11.040. Epub 2008 Nov 25.

DOI:10.1016/j.aca.2008.11.040
PMID:19427481
Abstract

Multivariate curve resolution-alternating least squares (MCR-ALS) of multi-experiment data analysis was successfully applied to elucidate the photodynamics of the N-(3-methylsalicylidene)-3-methylaniline by analyzing UV-vis femtosecond transient absorption spectra. The two-way data obtained present some specific difficulties linked to the nature of the transient spectra collected and to the overlapping of the photodynamics of the solvent and other contributions at short time scale (below 1 ps). Advantage was taken from the flexibility of the hybrid hard-soft multivariate curve resolution (HS-MCR) approach to consider a non-absorbing contribution in the kinetic model and to provide a functional description of the solvent in soft-modelling. The results obtained confirm the existence of an intermediate excited state in the process, which is created just after the ESIPT. It was observed that this intermediate relaxes in a few hundreds of femtosecond to the S(1) fluorescent cis-keto excited state and a decay time constant of 219 fs was found. These results confirm other femtosecond time-resolved fluorescence studies on salicylidene aniline molecules. Previous hypothesis on the formation of the trans-keto photoproduct from the S(1) fluorescent cis-keto state (time constant 14 ps) is also confirmed.

摘要

多实验数据分析的多元曲线分辨交替最小二乘法(MCR-ALS)通过分析紫外-可见飞秒瞬态吸收光谱,成功应用于阐明N-(3-甲基亚水杨基)-3-甲基苯胺的光动力学。所获得的双向数据存在一些特定困难,这些困难与所收集瞬态光谱的性质以及在短时间尺度(低于1皮秒)下溶剂光动力学和其他贡献的重叠有关。利用混合硬-软多元曲线分辨(HS-MCR)方法的灵活性,在动力学模型中考虑非吸收贡献,并在软建模中提供溶剂的功能描述。所得结果证实了该过程中存在一个中间激发态,它在ESIPT之后立即产生。观察到该中间体在几百飞秒内弛豫到S(1)荧光顺式酮激发态,并发现其衰减时间常数为219飞秒。这些结果证实了其他关于亚水杨基苯胺分子的飞秒时间分辨荧光研究。先前关于从S(1)荧光顺式酮态(时间常数14皮秒)形成反式酮光产物的假设也得到了证实。

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引用本文的文献

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