影响发光镧系希夫碱配合物能量传递途径的因素

IF 2.7 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR
Najat A. Al Riyami, Nawal K. Al-Rasbi
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引用次数: 0

摘要

在过去的几十年中,希夫碱配体的镧系元素(III)配合物因其奇妙的发光特性而备受关注。因此,它们的配合物被广泛应用于光学、生物和环境领域。本综述研究了镧系元素(III)希夫碱配合物的结构和敏化方面。通过有效的能量转移途径诱导其发光特性的因素,如(1)金属的几何形状,(2)配体的设计和优先结合模式,(3)温度和(4)分子聚集,都得到了深入的讨论。此外,还详细讨论了由 (1) 配体内电荷转移(ILCT)、(2) 配体到金属的电荷转移(LMCT)、(3) 配体-配体相互作用(LLI)或 (4) 单个分子中的混合 d-f 或 f-f 激发态引发的低洼激发三重态的性质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Factors that influence the energy transfer pathways in luminescent lanthanide Schiff base complexes

Factors that influence the energy transfer pathways in luminescent lanthanide Schiff base complexes

In the past decades, lanthanide(III) complexes from the Schiff base ligands have received attention for their marvelous luminescence properties. Accordingly, their complexes have been used in a variety of applications in optical, biological and environmental fields. In this review, the structural and sensitization aspects of the lanthanide(III) Schiff base complexes have been investigated. The factors that induce their luminescence properties through efficient energy transfer pathways have been discussed thoroughly, such as (1) metal’s geometry, (2) ligand’s design and the preferred binding modes, (3) temperature and (4) molecular aggregation. In addition, the nature of the low-lying excited triplet state initiated from (1) intra-ligand charge transfer, ILCT, (2) ligand to metal charge transfer, LMCT, (3) ligand–ligand interaction, LLI, or (4) mixed d-f or f-f excited states in a single molecule, have also been discussed in detail.

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来源期刊
Inorganica Chimica Acta
Inorganica Chimica Acta 化学-无机化学与核化学
CiteScore
6.00
自引率
3.60%
发文量
440
审稿时长
35 days
期刊介绍: Inorganica Chimica Acta is an established international forum for all aspects of advanced Inorganic Chemistry. Original papers of high scientific level and interest are published in the form of Articles and Reviews. Topics covered include: • chemistry of the main group elements and the d- and f-block metals, including the synthesis, characterization and reactivity of coordination, organometallic, biomimetic, supramolecular coordination compounds, including associated computational studies; • synthesis, physico-chemical properties, applications of molecule-based nano-scaled clusters and nanomaterials designed using the principles of coordination chemistry, as well as coordination polymers (CPs), metal-organic frameworks (MOFs), metal-organic polyhedra (MPOs); • reaction mechanisms and physico-chemical investigations computational studies of metalloenzymes and their models; • applications of inorganic compounds, metallodrugs and molecule-based materials. Papers composed primarily of structural reports will typically not be considered for publication.
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