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首页> 外文期刊>Bulletin of the Korean Chemical Society >Phosphorescent Iridium(III) Cyclometalates Supported by 2-(1,2-Dihydronaphthalen-4-yl)pyridine Ligand
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Phosphorescent Iridium(III) Cyclometalates Supported by 2-(1,2-Dihydronaphthalen-4-yl)pyridine Ligand

机译:磷光铱(III)由2-(1,2-二氢萘-4-基-4-基)吡啶配体负载的环荷酸酯

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摘要

Novel Ir(III) cyclometalates, (dnpy)(2)Ir(acac) (2) and fac-Ir(dnpy)(3) (3), supported by 2-(1,2-dihydronaphthalen- 4-yl) pyridyl ligand (dnpy) were synthesized and characterized. X-ray diffraction study on 3 revealed facial arrangement of three dnpy ligands around the Ir center. Photoluminescence (PL) spectra of 2 exhibited orange emission centered at 590 nm, which is almost similar to that observed for 2naphthylpyridine complex, (napy) 2Ir(acac) (III). In contrast, compound 3 displayed blue-shifted, yellow emission at 550 nm. Tris-complex 3 showed higher quantum efficiencies than 2 in both the solution and film states. Cyclic voltammetry measurements indicated that replacing naphthyl with 1,2-dihydronaphthyl ring raises both the metal-centered HOMO level and ligand-centered LUMO level in 2 and 3. It was suggested that 1,2-dihydronaphthyl ring has a stronger electron-donating effect than naphthyl ring, while the p* orbital of dnpy ligand is less stabilized due to partial conjugation of the dihydronaphthyl ring.
机译:合成并表征了以2-(1,2-二氢萘-4-基)吡啶配体(dnpy)为载体的新型Ir(III)环金属酸酯(dnpy)(2)Ir(acac)(2)和fac Ir(dnpy)(3)(3)。X射线衍射研究表明,3个dnpy配体在红外中心周围呈面状排列。2的光致发光(PL)光谱显示出以590 nm为中心的橙色发射,这几乎与观察到的2Naphythylpridine络合物(napy)2Ir(acac)(III)的光致发光类似。相比之下,化合物3在550 nm处显示蓝移黄色发射。Tris络合物3在溶液和薄膜状态下的量子效率均高于2。循环伏安法测量表明,用1,2-二氢萘环取代萘基可提高2和3中以金属为中心的HOMO水平和以配体为中心的LUMO水平。结果表明,1,2-二氢萘环比萘环具有更强的给电子效应,而dnpy配体的p*轨道由于二氢萘环的部分共轭而不太稳定。

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