Suppr超能文献

配体辅助的Tb 配合物中反向能量转移用于热感性质。

Ligand-Assisted Back Energy Transfer in Luminescent Tb Complexes for Thermosensing Properties.

机构信息

Graduate School of Chemical Sciences and Engineering, Hokkaido University, North 13 West 8, Kita-ku, Sapporo, Hokkaido, 060-8628, Japan.

Faculty of Engineering, Hokkaido University, North 13 West 8, Kita-ku, Sapporo, Hokkaido, 060-8628, Japan.

出版信息

Chemistry. 2018 Dec 3;24(67):17719-17726. doi: 10.1002/chem.201804392. Epub 2018 Nov 22.

Abstract

A luminescent Tb complex with a hexafluoroacetylacetone (hfa) ligand shows a characteristic back energy transfer (BEnT), which leads to high temperature sensitivity and potential application as a thermosensitive paint. Ligand-assisted BEnT was observed when a phosphine oxide ligand was introduced into Tb(hfa) complex, which was shown to affect the activation energy (ΔE ) and frequency factor (A) in the BEnT process between Tb ion and hfa ligands. According to temperature-dependent emission-lifetime measurements of mononuclear Tb(hfa) complexes with monodentate phosphine oxides and polynuclear Tb(hfa) complexes with bidentate phosphine oxides, the ΔE and A values of polynuclear Tb complexes were smaller than those of mononuclear Tb complexes. Phosphorescence spectra and lifetimes of each Gd(hfa) complex revealed that excited states of hfa ligands in Tb complexes differed from those of the polynuclear Tb complexes and mononuclear Tb complexes. The differences in the ΔE and A values between polynuclear and mononuclear Tb complexes were caused by the formation of different excited states, such as delocalization of the excited state in the polynuclear Tb complexes and localization of excited states in the mononuclear Tb complexes. In particular, small ΔE and A values of polynuclear Tb complexes provided high, effective activation of the BEnT at low temperature, which resulted in high-sensitive temperature-dependent phosphor materials over a wide temperature range.

摘要

具有六氟乙酰丙酮 (hfa) 配体的发光 Tb 配合物显示出特征的反向能量转移 (BEnT),这导致其具有高的温度敏感性和作为热敏涂料的潜在应用。当在 Tb(hfa) 配合物中引入膦氧化物配体时,观察到配体辅助的 BEnT,这表明其影响了 Tb 离子和 hfa 配体之间 BEnT 过程中的活化能 (ΔE) 和频率因子 (A)。根据单核 Tb(hfa) 配合物与单核膦氧化物和多核 Tb(hfa) 配合物与双膦氧化物的温度依赖性发射寿命测量,多核 Tb 配合物的 ΔE 和 A 值小于单核 Tb 配合物的。每个 Gd(hfa) 配合物的磷光光谱和寿命表明,Tb 配合物中 hfa 配体的激发态与多核 Tb 配合物和单核 Tb 配合物的激发态不同。多核和单核 Tb 配合物之间 ΔE 和 A 值的差异是由不同激发态的形成引起的,例如多核 Tb 配合物中激发态的离域和单核 Tb 配合物中激发态的局域化。特别是,多核 Tb 配合物的小 ΔE 和 A 值在低温下提供了 BEnT 的高、有效激活,从而在宽温度范围内提供了高灵敏度的温度依赖性磷光材料。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验