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Systematic Investigation of the Metal-Structure-Photophysics Relationship of Emissive d~(10)-Complexes of Group 11 Elements: The Prospect of Application in Organic Light Emitting Devices

机译:d〜(10)-第11族元素​​配合物的金属-结构-光物理关系的系统研究:在有机发光器件中的应用前景

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摘要

A series of new emissive group 11 transition metal d~(10)-complexes 1—8 bearing functionalized 2-pyridyl pyrrolide together with phosphine ancillary such as bis [2-(diphenylphosp- hino)phenyl] ether (POP) or PPh_3 are reported. The titled complexes are categorized into three classes, i.e. Cu(Ⅰ) complexes (1-3), Ag(Ⅰ) complexes (4 and 5), and Au(Ⅰ) metal complexes (6-8). Via combination of experimental and theoretical approaches, the group 11 d~(10)-metal ions versus their structural variation, stability, and corresponding photophysical properties have been investigated in a systematic and comprehensive manner. The results conclude that, along the same family, how much a metal d-orbital is involved in the electronic transition plays a more important role than how heavy the metal atom is, i.e. the atomic number, in enhancing the spin—orbit coupling. The metal ions with and without involvement of a d orbital in the lowest lying electronic transition are thus classified into internal and external heavy atoms, respectively. Cu(Ⅰ) complexes 1-3 show an appreciable metal d contribution (i.e., MLCT) in the lowest lying transition, so that Cu(Ⅰ) acts as an internal heavy atom. Despite its smallest atomic number among group 11 elements, Cu(Ⅰ) complexes 1-3 exhibit a substantially larger rate of intersystem crossing (ISC) and phosphorescence radiative decay rate constant (k_r~p) than those of Ag(Ⅰ) (4 and 5) and Au(Ⅰ) (6-8) complexes possessing pure π→π* character in the lowest transition. Since Ag(I) and Au(I) act only as external heavy atoms in the titled complexes, the spin—orbit coupling is mainly governed by the atomic number, such that complexes associated with the heavier Au(O) (6—8) show faster ISC and larger k_r~p than the Ag(I) complexes (4 and 5). This trend of correlation should be universal and has been firmly supported by experimental data in combination with empirical derivation. Along this line, Cu(I) complex 1 exhibits intensive phosphorescence (Φ_P = 0.35 in solid state) and has been successfully utilized for fabrication of OLEDs, attaining peak EL efficiencies of 6.6%, 20.0 cd/A, and 14.9 lm/W for the forward directions.
机译:报道了一系列带有官能化的2-吡啶基吡咯化物的新型11族过渡金属d〜(10)-配合物1-8,以及膦辅助化合物,例如双[2-(二苯基膦基)苯基]醚(POP)或PPh_3 。标题的络合物分为三类,即Cu(Ⅰ)络合物(1-3),Ag(Ⅰ)络合物(4和5)和Au(Ⅰ)金属络合物(6-8)。通过实验和理论方法的结合,系统地,全面地研究了11 d〜(10)族金属离子与其结构变异,稳定性和相应的光物理性质。结果得出结论,在同一个族中,金属d轨道参与电子跃迁的作用比金属原子(即原子数)的重在增强自旋-轨道耦合方面起着更为重要的作用。因此,在最低的电子跃迁中具有和不具有d轨道的金属离子分别分类为内部和外部重原子。 Cu(Ⅰ)配合物1-3在最低的跃迁中显示出相当大的金属d贡献(即,MLCT),因此Cu(Ⅰ)充当内部重原子。尽管Cu(Ⅰ)配合物1-3在11族元素​​中原子序数最小,但其系统间穿越(ISC)速率和磷光辐射衰变速率常数(k_r〜p)比Ag(Ⅰ)(4和5)和Au(Ⅰ)(6-8)配合物在最低跃迁中具有纯π→π*特征。由于Ag(I)和Au(I)仅在标题的络合物中充当外部重原子,因此自旋-轨道耦合主要受原子序数的控制,使得络合物与较重的Au(O)(6-8)相关与Ag(I)配合物(4和5)相比,具有更快的ISC和更大的k_r〜p。这种相关趋势应该是普遍的,并得到实验数据和经验推论的坚定支持。沿着这条线,Cu(I)配合物1表现出强烈的磷光(固态时Φ_P= 0.35),并已成功地用于制造OLED,达到了6.6%,20.0 cd / A和14.9 lm / W的峰值EL效率。前进方向。

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  • 来源
    《Journal of the American Chemical Society》 |2011年第31期|p.12085-12099|共15页
  • 作者单位

    Department of Chemistry, National Tsing Hua University, Hsinchu 30013, Taiwan;

    Department of Chemistry, National Taiwan University, Taipei 10617, Taiwan;

    Department of Chemistry, National Taiwan University, Taipei 10617, Taiwan;

    Department of Chemistry, National Tsing Hua University, Hsinchu 30013, Taiwan;

    Department of Chemistry, National Taiwan University, Taipei 10617, Taiwan;

    Department of Chemistry, National Taiwan University, Taipei 10617, Taiwan;

    Department of Photonics Engineering, Yuan Ze University, Chungli 32003, Taiwan;

    Department of Photonics Engineering, Yuan Ze University, Chungli 32003, Taiwan;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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