Luminescence of lanthanide complexes: From fundamental to prospective approaches related to water- and molecular-stimuli

Miki Hasegawa , Hitomi Ohmagari , Hideyuki Tanaka , Kanade Machida
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Abstract

Luminescent lanthanide (Ln) complexes are attracted much attention because of their stable emission colors induced by the photo-antenna effect through the photo-excited energy transfer from aromatic ligands to Ln ions. Here, we will introduce some systems of luminescent Ln complexes with metastable states with the phase transition induced by water and other small molecules, the relative arrangement of hydrogel formation and Ln luminescence enhancement, and the diversity of the thin air-water interface. The energy donor levels in each system should be designed to sensitize Ln-luminescence with the consideration of media, interaction and assembling. Luminescence quenching of Ln complexes in water is a point that should be considered for the development of materials and for the purpose of bio-related materials. Then, the principle of the change in luminescence intensity by the effect of water molecules is described, and the estimation of a hydrated structure of the complex is estimated using the luminescence lifetimes in H2O and D2O. The molecular arrangement of these crystals changes under the vapor-stimuli, and the coloration and luminescence may be enhanced. Some interesting cases of luminescent Ln complexes with the crystal-to-crystal phase transitions will be introduced with the vapor adsorption. Hydrogels are mostly water by volume; a system in which Ln luminescence is maintained implies that Ln ions are placed in hydrophobic positions in self-assemblies with strong luminescence. The formation of thin films at the molecular level and their Ln luminescence properties are introduced. For example, when a monolayer of a surface-active Ln complex is formed at the air-water interface, the repeated accumulation of the flexible film forms a metastable structure with a regular structure different from that of a crystal, and no water is incorporated into the film. These can not only derive circularly or linearly polarized light, but also take in other molecules and change the emission. Finally, we will suggest the prospects for the development of Ln complexes.

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镧系配合物的发光:从基础到与水和分子刺激相关的前瞻性方法
发光镧系化合物(Ln)配合物因其具有稳定的发光颜色而受到广泛关注,这种发光颜色是由芳族配体光激发能量向镧离子转移而产生的光天线效应引起的。本文将介绍一些由水和其他小分子诱导相变的亚稳态发光Ln配合物体系,水凝胶形成和Ln发光增强的相对排列,以及稀薄空气-水界面的多样性。考虑介质、相互作用和组装等因素,每个系统的供能能级应设计成能敏化镧发光。Ln配合物在水中的发光猝灭是材料开发和生物相关材料开发应考虑的问题。然后,描述了水分子作用下发光强度变化的原理,并利用在H2O和D2O中的发光寿命估计了配合物的水合结构。在蒸汽刺激下,这些晶体的分子排列发生了变化,显色性和发光性增强。本文将介绍一些具有晶体到晶体相变的发光Ln配合物的有趣例子。按体积计算,水凝胶主要是水;一个保持Ln发光的系统意味着Ln离子在具有强发光的自组装体中被放置在疏水位置。介绍了分子水平上薄膜的形成及其发光特性。例如,当在空气-水界面形成表面活性Ln配合物的单层时,柔性膜的反复积累形成与晶体不同的规则结构的亚稳结构,并且不将水掺入膜中。它们不仅可以产生圆偏振光或线偏振光,还可以吸收其他分子并改变发射。最后,对Ln配合物的发展前景进行了展望。
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来源期刊
CiteScore
21.90
自引率
0.70%
发文量
36
审稿时长
47 days
期刊介绍: The Journal of Photochemistry and Photobiology C: Photochemistry Reviews, published by Elsevier, is the official journal of the Japanese Photochemistry Association. It serves as a platform for scientists across various fields of photochemistry to communicate and collaborate, aiming to foster new interdisciplinary research areas. The journal covers a wide scope, including fundamental molecular photochemistry, organic and inorganic photochemistry, photoelectrochemistry, photocatalysis, solar energy conversion, photobiology, and more. It provides a forum for discussing advancements and promoting collaboration in the field of photochemistry.
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