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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Tuning the electronic and phosphorescence properties of blue-emitting iridium(III) complexes through different cyclometalated ligand substituents: a theoretical investigation
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Tuning the electronic and phosphorescence properties of blue-emitting iridium(III) complexes through different cyclometalated ligand substituents: a theoretical investigation

机译:通过不同的环金属化配体取代基调节发蓝光的铱(III)配合物的电子和磷光性质:理论研究

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The geometric and electronic structures, phosphorescence properties and the organic light-emitting diode (OLED) performance of a series of Ir(III) complexes based on bis[(4,6-di-fluorophenyl)-pyridinato-N,C2']picolinate (FIrpic) were investigated by using density functional theory/time-dependent density functional theory (DFT/TD-DFT),including Ir(III)bis[2-(2,4-difluorophenyl)-4-(tert-butyl)pyridinato-N,C2']picolinate (1a), Ir(III)bis[2-(2,4-difluorophenyl)-4-(n-heptyl)pyridinato-N,C2']picolinate (2a), Ir(III)bis[2-(2,4-difluorophenyl)-4-(3-ethylheptyl)pyridinato-N,C2']picolinate (3a), Ir(III)bis[2-(2,4-difluorophenyl)-4-(2,4,6-trimethylphenyl)pyridinato-N,C2']picolinate (5a), and Ir(III)bis[2-(2,4-difluoro-3-(2,4,6-trimethylphenyl)phenyl)-pyridinato-N,C2'] picolinate (5b). To explore the influence of the substituted positions on the optical and electronic properties of the Ir(III) complexes, seven other new complexes were designed by introducing the substituted groups on the difluorophenyl rings or pyridine rings. After introducing the phenyl substituted groups on the pyridine or difluorophenyl rings of cyclometalated ligands, the HOMO-LUMO energy gap is decreased. Thus, the absorption spectra of 4a and 4b undergo a red-shifting, especially for 4a, and have a stronger absorption strength that will be beneficial to improving their quantum yields, which is proved by the further evaluation of the radiative (k(r)) and non-radiative (k(nr)) rate constants. The combinations of a larger (MLCT)-M-3-(MC)-M-3 energy gap, smaller Delta ES1-T1, and higher contribution of (MLCT)-M-3 in the emission process result in the higher quantum yields for complexes 4a and 4b. Besides, the designed complexes 4a and 4b are considered to be potential candidates as blue-emitting materials with better equilibrium between the hole transport (lambda(hole)) and electron transport (lambda(electron)).
机译:一系列基于双[(4,6-二氟苯基)-吡啶基-N,C2']吡啶甲酸酯的Ir(III)配合物的几何和电子结构,磷光性质和有机发光二极管(OLED)性能通过使用密度泛函理论/随时间变化的密度泛函理论(DFT / TD-DFT)研究了(FIrpic),包括Ir(III)bis [2-(2,4-二氟苯基)-4-(叔丁基)吡啶并-N,C2']吡啶甲酸(1a),Ir(III)双[2-(2,4-二氟苯基)-4-(正庚基)吡啶基-N,C2']吡啶甲酸(2a),Ir(III)双[2-(2,4-二氟苯基)-4-(3-乙基庚基)吡啶基-N,C2']吡啶甲酸酯(3a),Ir(III)双[2-(2,4-二氟苯基)-4-( 2,4,6-三甲基苯基)吡啶基-N,C2']吡啶甲酸(5a)和Ir(III)双[2-(2,4-二氟-3-(2,4,6-三甲基苯基)苯基)-吡啶并-N,C2']吡啶甲酸(5b)。为了探索取代位置对Ir(III)配合物的光学和电子性质的影响,通过在二氟苯基环或吡啶环上引入取代基,设计了另外七个新配合物。在环金属化配体的吡啶或二氟苯基环上引入苯基取代基后,HOMO-LUMO能隙减小。因此,4a和4b的吸收光谱会发生红移,尤其是4a的吸收光谱,并且具有更强的吸收强度,这将有利于提高其量子产率,这通过进一步评估辐射(k(r) )和非辐射(k(nr))速​​率常数。 (MLCT)-M-3-(MC)-M-3能隙,较小的Delta ES1-T1和(MLCT)-M-3在发射过程中的较高贡献的组合导致较高的量子产率用于配合物4a和4b。此外,设计的络合物4a和4b被认为是潜在的候选物,作为在空穴传输(λ)和电子传输(λ(电子))之间具有更好平衡的发蓝光材料。

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