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含 5-苯基-1-1,2,4-三唑型环金属配体的阳离子铱配合物:向蓝色位移发射的研究。

Cationic Iridium Complexes with 5-Phenyl-1-1,2,4-triazole Type Cyclometalating Ligands: Toward Blue-Shifted Emission.

机构信息

College of Chemistry, Key Laboratory of Pesticide and Chemical Biology of Ministry of Education, Hubei International Scientific and Technological Cooperation Base of Pesticide and Green Synthesis, International Joint Research Center for Intelligent Biosensing Technology and Health , Central China Normal University , Wuhan 430079 , People's Republic of China.

Key Lab of Organic Optoelectronics and Molecular Engineering of Ministry of Education, Department of Chemistry , Tsinghua University , Beijing 100084 , People's Republic of China.

出版信息

Inorg Chem. 2019 Sep 16;58(18):12132-12145. doi: 10.1021/acs.inorgchem.9b01433. Epub 2019 Aug 29.

Abstract

Four cationic iridium complexes with 5-phenyl-1-1,2,4-triazole (phtz) type cyclometalating ligands (C^N) and different ancillary ligands (N^N), namely, [Ir(dphtz)(bpy)]PF (), [Ir(dphtz)(pzpy)]PF (), [Ir(Mephtz)(pzpy)]PF (), and [Ir(Mephtz)(dma-pzpy)]PF (), have been designed, synthesized, and fully characterized (dphtz = 1-(2,6-dimethylphenyl)-3-methyl-5-phenyl-1-1,2,4-triazole, Mephtz = 1,3-dimethyl-5-phenyl-1-1,2,4-triazole; bpy = 2,2'-bipyridine, pzpy = 2-(1-pyrazol-1-yl)pyridine, dma-pzpy = 4-dimethylamino-2-(1-pyrazol-1-yl) pyridine). In solution, complex emits efficient yellow light (λ = 547 nm), which is blue-shifted by nearly 40 nm (or by 1187 cm) compared with that from the archetypal complex [Ir(ppy)(bpy)]PF (Hppy = 2-phenylpyridine), owing to the stabilization of the highest occupied molecular orbital by the phtz-type C^N ligand. In the lightly doped rigid films, complex emits green light with a high luminescent efficiency of 0.89. Although complexes - with electron-rich N^N ligands are weakly emissive or nearly nonemissive in the solution, they emit relatively strong deep-blue light peaked around 435 and 461 nm in the lightly doped films, which is among the bluest reported for cationic iridium complexes. Theoretical calculations reveal that for complex , the emission always comes from the charge-transfer (CT) (Ir/C^N → N^N) state; for complexes and , the CT and C^N-centered π-π* states lie close in energy and the emission could originate from either or both of them; for complex , the emission comes predominantly from the C^N-centered π-π* state. For blue-emitting complexes -, metal-centered states play an active role in the nonradiative deactivation of the emitting triplet states. Solid-state light-emitting electrochemical cells (LECs) based on complexes - show yellow-green, blue, and blue-green electroluminescence, respectively, with the yellow-green LEC affording a peak current efficiency of 21.5 cd A.

摘要

四种带有 5-苯基-1-1,2,4-三唑(phtz)型环金属配体(C^N)和不同辅助配体(N^N)的阳离子铱配合物,即[Ir(dphtz)(bpy)]PF ()、[Ir(dphtz)(pzpy)]PF ()、[Ir(Mephtz)(pzpy)]PF ()和[Ir(Mephtz)(dma-pzpy)]PF (),已经被设计、合成并进行了充分的表征(dphtz = 1-(2,6-二甲基苯基)-3-甲基-5-苯基-1-1,2,4-三唑,Mephtz = 1,3-二甲基-5-苯基-1-1,2,4-三唑;bpy = 2,2'-联吡啶,pzpy = 2-(1-吡唑-1-基)吡啶,dma-pzpy = 4-二甲基氨基-2-(1-吡唑-1-基)吡啶)。在溶液中,配合物 发出高效的黄色光(λ = 547nm),与原型配合物[Ir(ppy)(bpy)]PF (Hppy = 2-苯基吡啶)相比,它的发射光谱蓝移了近 40nm(或 1187cm),这是由于 phtz 型 C^N 配体稳定了最高占据分子轨道。在轻度掺杂的刚性薄膜中,配合物 发出绿光,发光效率高达 0.89。尽管配合物 - 带有富电子的 N^N 配体,在溶液中是弱发光或几乎不发光,但在轻度掺杂的薄膜中,它们发出相对较强的深蓝色光,峰值在 435nm 和 461nm 左右,这是阳离子铱配合物中报道的最蓝的光之一。理论计算表明,对于配合物 ,发射总是来自电荷转移(CT)(Ir/C^N → N^N)态;对于配合物 和 ,CT 和 C^N 中心的 π-π态能量相近,发射可能来自其中之一或两者;对于配合物 ,发射主要来自 C^N 中心的 π-π态。对于蓝色发射的配合物 - ,金属中心态在发射三重态的非辐射失活中起着积极的作用。基于配合物 - 的固态电致发光电化学电池(LEC)分别显示出黄绿光、蓝光和蓝绿光电致发光,其中黄绿光 LEC 的峰值电流效率为 21.5cdA。

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