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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:2-(1,2-二氢萘-4-基)吡啶配体支持的磷化铱(III)环金属盐

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Novel Ir(III) cyclometalates, (dnpy) 2Ir(acac) (2) and faca??Ir(dnpy)3 (3), supported by 2a??(1,2a??dihydronaphthalena??4a??yl)pyridyl ligand (dnpy) were synthesized and characterized. Xa??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 590a??nm, which is almost similar to that observed for 2a??naphthylpyridine complex, (napy) 2Ir(acac) ( III ). In contrast, compound 3 displayed bluea??shifted, yellow emission at 550a??nm. Trisa??complex 3 showed higher quantum efficiencies than 2 in both the solution and film states. Cyclic voltammetry measurements indicated that replacing naphthyl with 1,2a??dihydronaphthyl ring raises both the metala??centered HOMO level and liganda??centered LUMO level in 2 and 3. It was suggested that 1,2a??dihydronaphthyl ring has a stronger electrona??donating effect than naphthyl ring, while the ??* orbital of dnpy ligand is less stabilized due to partial conjugation of the dihydronaphthyl ring.
机译:新型Ir(III)环金属盐(dnpy)2Ir(acac)(2)和faca ?? Ir(dnpy)3(3),由2a ??(1,2a ??二氢萘?? 4a ??基)吡啶基支撑合成并表征了配体(dnpy)。 X射线衍射研究表明3周围Ir中心的三个dnpy配体的面部排列。 2的光致发光(PL)光谱显示出以590a -1 nm为中心的橙色发射,这几乎与2a -18萘吡啶配合物(napy)2Ir(acac)(III)所观察到的相似。相反,化合物3在550a -1 nm处显示出蓝移的,黄移的。在溶液态和膜态下,Trisaα-络合物3均显示出比2更高的量子效率。循环伏安法测量表明,用1,2a ??二氢萘基环取代萘基可同时提高2和3中以金属a ??中心的HOMO能级和以配体a?中心的LUMO能级。这表明1,2a ??二氢萘基环具有更强的电子给体的供电作用比萘环大,而dnpy配体的?? *轨道由于二氢萘环的部分共轭而不稳定。

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