Efficient IrIII Photosensitizer Incorporated in the Metal-Organic Framework with the Bis-lophine-bipyridine Motif for C(sp3)-C/N-H Cross-Coupling Reactions

被引:3
|
作者
Chen, Yuan [1 ]
Liu, Ao-Gang [1 ]
Chen, Zi-Tong [1 ]
Liang, Xiao-Huan [1 ]
Yan, Jun-Tao [1 ]
Li, Bao [1 ]
机构
[1] Huazhong Univ Sci & Technol, Sch Chem & Chem Engn, Hubei Key Lab Bioinorgan Chem & Mat Med, Semicond Chem Ctr,Key Lab Mat Chem Energy Convers, Wuhan 430074, Hubei, Peoples R China
来源
ACS CATALYSIS | 2024年 / 14卷 / 22期
基金
中国国家自然科学基金;
关键词
metal-organic framework; bis-lophine-bipyridine; photocatalysis; iridium-based catalysts; light energy utilization efficiency; INTEGRATION;
D O I
10.1021/acscatal.4c04666
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Photocatalytic technology offers a potential solution to energy and environmental issues. The performance of photocatalysts directly affects the efficiency of photocatalysis. Iridium(III)-based catalysts have garnered attention due to their unique electronic structure and high catalytic activity. However, most Ir-III catalysts are homogeneous and face issues such as low stability and difficulty in recycling. The research on heterogeneous Ir-III catalysts has become a hot topic, aiming to improve their stability and recyclability. In this study, we designed a tetracarboxylate ligand containing bipyridine modified with a bilophthalene unit, constructed a Zr-based metal-organic framework (MOF) with a 2-fold interpenetrating structure, and introduced [Ir-III(ppy)(2)](+) units through postmodification to form Ir@Zr-MOF. The heterostructure enhanced the utilization of light energy and photocatalytic efficiency. Apart from the electron transfer pathway between the original zirconium clusters and the bislophine-bipyridine unit, comparative studies of theoretical models showed that the introduction of the [Ir-III(ppy)(2)](+) unit reduced the energy level and enhanced the absorption of visible light in the 500-550 nm range, corresponding to the charge transfer between the modified bis-lophine-bipyridine and [Ir-III(ppy)(2)](+) unit. Ir@Zr-MOF, as a photocatalyst, can facilitate the trifluoromethylation of coumarins and the oxidative dehydrogenative coupling reaction of ethers with aryl hydrazones. The conversion yields of the related reactions can reach up to 95%. The mechanism presumes that the generation of superoxide radicals and the corresponding holes produced by Ir@Zr-MOF are crucial for the photocatalytic reaction. The generation of superoxide radicals can be verified by ESR. The host-guest interactions and hole effects of Ir@Zr-MOF with reaction substrates were also explored through theoretical simulations. This work provides a strategy for the heterogenization of Ir-III catalysts, offering insights for the preparation of photosensitizers and the enhancement of light energy utilization.
引用
收藏
页码:16605 / 16617
页数:13
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