A multi-property fluorescent probe for the investigation of polymer dynamics near the glass transition

J. Siekierzycka, Catharina Hippius, F. Würthner, René M. Williams, A. Brouwer
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引用次数: 3

Abstract

In addition to the commonly observed single molecule fluorescence intensity fluctuations due to molecular reorientation dynamics, a perylene bisimide-calixarene compound (1) shows additional on-off fluctuations due to its ability to undergo intramolecular excited state electron transfer (PET). This quenching process is turned on rather sharply when a film of poly(vinylacetate) containing 1 is heated above its glass transition temperature (Tg), which indicates that the electron transfer process depends on the availability of sufficient free volume. Spatial heterogeneities cause different individual molecules to reach the electron transfer regime at different temperatures, but these heterogeneities also fluctuate in time: in the matrix above Tg molecules that are mostly nonfluorescent due to PET can become fluorescent again on timescales of seconds to minutes.The two different mechanisms for intensity fluctuation, rotation and PET, thus far only observed in compound 1, make it a unique probe for the dynamics of supercooled liquids.
用于研究玻璃化转变附近聚合物动力学的多性能荧光探针
除了通常观察到的由于分子重定向动力学引起的单分子荧光强度波动外,苝二酰亚胺-桥芳烃化合物(1)由于其能够进行分子内激发态电子转移(PET)而表现出额外的开关波动。当含有1的聚醋酸乙烯酯薄膜加热到其玻璃化转变温度(Tg)以上时,这种淬火过程就会急剧开启,这表明电子转移过程取决于足够的自由体积的可用性。空间异质性导致不同的单个分子在不同的温度下达到电子转移状态,但这些异质性也随时间波动:在Tg以上的矩阵中,由于PET而大部分非荧光的分子可以在秒到分钟的时间尺度上再次荧光。迄今为止仅在化合物1中观察到的两种不同的强度波动机制,旋转和PET,使其成为过冷液体动力学的独特探针。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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