Reversible Change between Excimer and Monomer Forms of Perylene Induced by Water Absorption and Dehydration of Poly-N-isopropylacrylamide Gel
Reversible Change between Excimer and Monomer Forms of Perylene Induced by Water Absorption and Dehydration of Poly-N-isopropylacrylamide Gel
复制标题
聚-N-异丙基丙烯酰胺凝胶吸水和脱水引起苝准分子和单体形态的可逆变化
DOI:
10.1021/acs.jpcb.0c11418
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发表时间:
2021
期刊:
影响因子:
3.3
通讯作者:
S. Ozeki
中科院分区:
文献类型:
--
作者:
A. Hamasaki;K. Kubo;M. Harashima;A. Katsuki;S. Ozeki
Several fluorescence patterns derived from the excimer states of perylene have been reported, but most of these have been obtained from rigid forms such as crystals or for perylene embedded in hard polymers. We observed perylene excimer emission on absorption of water by a poly-N-isopropylacrylamide gel containing perylene molecules, which were not fixed to the gel framework by chemical bonding. We propose that this emission arises because the hydrophobic perylene molecules cannot dissolve in water and form aggregates. The perylene aggregation was quickly lost on dehydration of the gel, and the luminescence reverted to that of the monomer. In a dehydrated environment, perylene was rapidly dispersed in the gel network. In other words, solid–liquid phase separation of perylene was induced by uptake of water into the gel, and perylene dissolved in the gel on dehydration. Because the outside of the gel is always in an aqueous environment, perylene will remain semipermanently in the gel. Therefore, monomer emission and excimer emission can be switched reversibly and repeatedly.