吡啶咪唑衍生双膦配体卤化铜一维聚合物的合成、表征及发光性能

IF 2.7 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR
Ming Liu, Qingqing Geng, Zhen Hu, Hang Qi, Shuang Liu, Chunmei Liu, Bin Zhang
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引用次数: 0

摘要

一维铜(I)配位聚合物(Cu - CPs),标记为CP1 (X = I), CP2 (X = Br)和CP3 (X = Cl),使用一种不寻常的吡啶咪唑双膦配体(L)和CuX构建。配体L增强了Cu中心周围的刚性,Cu−CPs表现出明亮的发光,最大发光波长分别为640 nm (CP1)、633 nm (CP2)和645 nm (CP3)。CP1的光致发光量子产率(PLQY)高达39%,在室温下的衰减寿命(τ)仅为0.77 μs,明显优于CP2 (PLQY: 14%, τ: 2.19 μs)和CP3 (PLQY: 6%, τ: 2.28 μs)。理论和实验研究表明,CP1的室温发光是由热激活延迟荧光(TADF)引起的。这项工作有望鼓励进一步探索基于Cu−CPs的有前途的发射器。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis, characterization and luminescent properties of copper(I) halide 1D polymers with pyridoimidazole−derived bisphosphine ligand
One−dimensional (1D) copper(I) coordination polymers (Cu − CPs), labeled CP1 (X = I), CP2 (X = Br), and CP3 (X = Cl), were constructed using an unusual pyridoimidazole−based bisphosphine ligand (L) and CuX. Ligand L enforces rigidity around the Cu centers, and the Cu − CPs exhibit bright luminescence, with emission maxima at 640 nm (CP1), 633 nm (CP2), and 645 nm (CP3), respectively. Due to the strong SOC effect and Cu(I) stabilization imparted by I, CP1 achieves a high photoluminescence quantum yield (PLQY) of 39 % and an exceptionally short decay lifetime (τ) of 0.77 μs at room temperature, significantly outperforming CP2 (PLQY: 14 %, τ: 2.19 μs) and CP3 (PLQY: 6 %, τ: 2.28 μs). Theoretical and experimental investigations suggest that the room−temperature luminescence of CP1 arises from thermally activated delayed fluorescence (TADF). This work is expected to encourage further exploration of promising emitters based on Cu − CPs.
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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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