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Effects of intramolecular and intermolecular interactions on excited state properties of two isomeric Cu complexes with AIE and TADF mechanisms in solid phase: A QM/MM study

机译:分子内和分子间相互作用对固相具有AIE和TADF机理的两种异构铜配合物的激发态性质的影响:QM / MM研究

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摘要

Molecular photophysical properties are not only related to the basic structures but also affected by their packing modes. In this work, excited state properties of two isomeric Cu complexes (Complex 1 and Complex 2) with aggregation induced emission (AIE) and thermally activated delayed fluorescence (TADF) features are theoretically studied. The surrounding environments for molecule in solution and solid phase are considered by polarizable continuum model (PCM) and the combined quantum mechanics and molecular mechanics (QM/MM) method respectively. In addition, the intermolecular interaction and intramolecular interaction are visualized by the reduced density gradient (RDG) function. Our investigations show that the geometrical changes between ground state (S-0) and lowest singlet excited state (S-1) are hindered in solid phase by the restricted intramolecular rotation (RIR) effect, which brings smaller Huang-Rhys factors. Moreover, the decreased reorganization energy from solution to solid phase, is mainly contributed by the reduction of dihedral angle in low frequency ( 500 cm(-1)) regions. Thus, non-radiative energy consumption process of S1 is hindered and AIE mechanism is revealed for two complexes. Furthermore, stronger intramolecular and intermolecular interactions in solid phase are found for Complex 1 than these for Complex 2, this brings decreased non-radiative decay rate and increased reverse intersystem crossing rate, remarkable prompt and delayed fluorescence efficiencies are detected for Complex 1. Thus, the effects of intramolecular and intermolecular interactions on photophysical properties of two AIE-Cu-TADF molecules are revealed and the experimental measurements are reasonably elucidated. Our work could promote molecular engineering for designing new efficient AIE-TADF materials in practical organic light emitting diodes (OLEDs).
机译:分子的光物理性质不仅与基本结构有关,而且还受其堆积方式的影响。在这项工作中,理论上研究了两种具有聚合诱导发射(AIE)和热激活延迟荧光(TADF)特征的异构铜配合物(配合物1和配合物2)的激发态性质。分别通过极化连续体模型(PCM)以及组合的量子力学和分子力学(QM / MM)方法来考虑溶液和固相中分子的周围环境。另外,分子间相互作用和分子内相互作用通过降低的密度梯度(RDG)功能可视化。我们的研究表明,受限制的分子内旋转(RIR)效应在固相中阻止了基态(S-0)和最低单线态激发态(S-1)之间的几何变化,这带来了较小的Huang-Rhys因子。此外,从溶液到固相的重组能降低,主要是由于低频(<500 cm(-1))区域的二面角减小所致。因此,阻碍了S1的非辐射能耗过程,并揭示了两种配合物的AIE机理。此外,发现配合物1的固相中分子内和分子间的相互作用强于配合物2的固相,这降低了非辐射衰减率,提高了反向系统间交叉速率,对于配合物1检测到了显着的迅速和延迟的荧光效率。因此,揭示了分子内和分子间相互作用对两个AIE-Cu-TADF分子光物理性质的影响,并合理阐明了实验测量值。我们的工作可能会促进分子工程学,以设计实用有机发光二极管(OLED)中的新型高效AIE-TADF材料。

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  • 来源
    《Organic Electronics》 |2019年第8期|113-122|共10页
  • 作者单位

    Shandong Normal Univ, Sch Phys & Elect, Inst Mat & Clean Energy, Shandong Prov Key Lab Med Phys & Image Proc Techn, Jinan 250014, Shandong, Peoples R China;

    Shandong Normal Univ, Sch Phys & Elect, Inst Mat & Clean Energy, Shandong Prov Key Lab Med Phys & Image Proc Techn, Jinan 250014, Shandong, Peoples R China;

    Shandong Normal Univ, Sch Phys & Elect, Inst Mat & Clean Energy, Shandong Prov Key Lab Med Phys & Image Proc Techn, Jinan 250014, Shandong, Peoples R China;

    Shandong Normal Univ, Sch Phys & Elect, Inst Mat & Clean Energy, Shandong Prov Key Lab Med Phys & Image Proc Techn, Jinan 250014, Shandong, Peoples R China;

    Shandong Normal Univ, Sch Phys & Elect, Inst Mat & Clean Energy, Shandong Prov Key Lab Med Phys & Image Proc Techn, Jinan 250014, Shandong, Peoples R China;

    Shandong Normal Univ, Sch Phys & Elect, Inst Mat & Clean Energy, Shandong Prov Key Lab Med Phys & Image Proc Techn, Jinan 250014, Shandong, Peoples R China;

    Shandong Normal Univ, Sch Phys & Elect, Inst Mat & Clean Energy, Shandong Prov Key Lab Med Phys & Image Proc Techn, Jinan 250014, Shandong, Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Aggregation induced emission; Thermally activated delayed fluorescence; Intramolecular and intermolecular interactions; QM/MM method;

    机译:聚集诱导发射;热激活延迟荧光;分子内和分子间相互作用;QM / MM方法;

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