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用于基于三重态-三重态湮灭的上转换的可见光收集环金属化 Ir(III) 配合物作为三重态光敏剂。

Visible light-harvesting cyclometalated Ir(III) complexes as triplet photosensitizers for triplet-triplet annihilation based upconversion.

机构信息

State Key Laboratory of Fine Chemicals, School of Chemical Engineering, Dalian University of Technology, E-208 West Campus, 2 Ling-Gong Road, Dalian 116012, PR China.

出版信息

Dalton Trans. 2012 Sep 21;41(35):10680-9. doi: 10.1039/c2dt30955f. Epub 2012 Jul 30.

Abstract

Visible light-harvesting cyclometalated Ir(III) complexes with 3-(2-benzothiazoly)-7-diethylaminocoumarin as the C^N cyclometalation ligands were prepared. The ancillary N^N ligand is either 6-piperidine naphthalimide-phenanthroline (Ir-1) or 9-aminophenanthroline (Ir-3). Ir(ppy)(2)(Phen) was prepared as model complex (Ir-2). Ir-1 and Ir-3 show strong absorption of visible light (ε = 109,000 M(-1) cm(-1) or 112,000 M(-1) cm(-1) at 486 or 484 nm, respectively). All the complexes show room temperature phosphorescence with drastically different phosphorescence quantum yields (Φ(P) = 4.3%, 44.3% and 46.0% for Ir-1, Ir-2 and Ir-3, respectively). With steady state and time-resolved spectra, as well as DFT calculations, the T(1) excited states of Ir-1 and Ir-3 were proposed to be the (3)IL state, whereas the (3)MLCT state was proposed for Ir-2. Long-lived emissive triplet excited states (7.6 μs and 54.5 μs) were observed for Ir-1 and Ir-3, compared to the short T(1) excited state lifetime of Ir-2 (1.2 μs). The complexes were used as triplet photosensitizers for triplet-triplet annihilation upconversion and upconversion quantum yields (Φ(UC)) of 19.3% and 12.7% were observed for Ir-1 and Ir-3, respectively. No upconversion was observed for Ir-2 under the same experimental conditions.

摘要

制备了以 3-(2-苯并噻唑基)-7-二乙氨基香豆素为 C^N 环金属化配体的可见光敏化环金属化 Ir(III) 配合物。辅助 N^N 配体为 6-哌啶萘酰亚胺-菲咯啉(Ir-1)或 9-氨基菲咯啉(Ir-3)。制备 Ir(ppy)(2)(Phen) 作为模型配合物(Ir-2)。Ir-1 和 Ir-3 在 486nm 或 484nm 处分别显示出可见光的强吸收(ε = 109,000M(-1)cm(-1)或 112,000M(-1)cm(-1))。所有配合物均显示室温磷光,磷光量子产率有很大差异(Ir-1、Ir-2 和 Ir-3 的磷光量子产率分别为 4.3%、44.3%和 46.0%)。通过稳态和时间分辨光谱以及 DFT 计算,提出 Ir-1 和 Ir-3 的 T(1)激发态为(3)IL 态,而 Ir-2 的(3)MLCT 态被提出。与 Ir-2 的短 T(1)激发态寿命(1.2μs)相比,Ir-1 和 Ir-3 观察到长寿命发射三重态激发态(7.6μs 和 54.5μs)。这些配合物被用作三重态光敏剂用于三重态-三重态湮灭上转换,观察到 Ir-1 和 Ir-3 的上转换量子产率(Φ(UC))分别为 19.3%和 12.7%。在相同的实验条件下,Ir-2 没有观察到上转换。

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