کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1325406 | 977382 | 2009 | 7 صفحه PDF | دانلود رایگان |
The ground and the lowest-lying triplet excited state geometries, electronic structures, and spectroscopic properties of a novel series of neutral iridium(III) complexes with cyclometalated alkenylquinoline ligands [(C^N)2Ir(acac)] (acac = acetoylacetonate; C^N = 2-[(E)-2-phenyl-1-ethenyl]pyridine (pep) 1; 2-[(E)-2-phenyl-1-ethenyl]quinoline (peq) 2; 1-[(E)-2-phenyl-1-ethenyl]isoquinoline (peiq) 3; 2-[(E)-1-propenyl]pyridine (pp) 4; 2-[(E)-1-fluoro-1-ethenyl]pyridine (fpp) 5) were investigated by DFT and CIS methods. The highest occupied molecular orbital is composed of d(Ir) and π(C^N) orbital, while the lowest unoccupied molecular orbital is dominantly localized on C^N ligand. Under the TD-DFT with PCM model level, the absorption and phosphorescence in CH2Cl2 media were calculated based on the optimized ground and triplet excited state geometries, respectively. The calculated lowest-lying absorptions at 437 nm (1), 481 nm (2), 487 nm (3), 422 nm (4), and 389 nm (5) are attributed to a {[dx2-y2dx2-y2(Ir) + dxz(Ir) + π(C^N)] → [π∗(C^N)]} transition with metal-to-ligand/intra-ligand charge transfer (MLCT/ILCT) characters, and the calculated phosphorescence at 582 nm (1), 607 nm (2), 634 nm (3), 515 nm (4), and 491 nm (5) can be described as originating from the 3{[dx2-y2dx2-y2(Ir) + dxz(Ir) + π (C^N)] [π∗(C^N)]} excited state with the 3MLCT/3ILCT characters. The calculated results revealed that the phosphorescent color of these new Ir(III) complexes can be tuned by changing the π-conjugation effect strength of the C^N ligand.
The present theoretical calculations on 1–5 showed that the phosphorescent color and the quantum efficiencies of these Ir(III) complexes can be tuned by changing the π-conjugation effect strength of the C^N ligand.Figure optionsDownload as PowerPoint slide
Journal: Journal of Organometallic Chemistry - Volume 694, Issue 2, 15 January 2009, Pages 150–156