Department of Chemistry, University of Nebraska-Lincoln, Lincoln, Nebraska 68588, United States.
Department of Chemistry, Marquette University, Milwaukee, Wisconsin 53201, United States.
J Am Chem Soc. 2021 Dec 8;143(48):20411-20418. doi: 10.1021/jacs.1c10291. Epub 2021 Nov 19.
In the past decades, many attempts have been made to mimic the energy transfer (EnT) in photosynthesis, a key process occurring in nature that is of fundamental significance in solar fuels and sustainable energy. Metal-organic frameworks (MOFs), an emerging class of porous crystalline materials self-assembled from organic linkers and metal or metal cluster nodes, offer an ideal platform for the exploration of directional EnT phenomena. However, placing energy donor and acceptor moieties within the same framework with an atomistic precision appears to be a major synthesis challenge. In this work, we report the design and synthesis of a highly porous and photoactive -bicarbazole- and porphyrin-based mixed-ligand MOF, namely, NPF-500-HTCPP (NPF = Nebraska porous framework; HTCPP = -tetrakis(4-carboxyphenyl)porphyrin), where the secondary ligand HTCPP is incorporated precisely through the open metal sites of the equatorial plane of the octahedron cage resulting from the underlying (4,8) connected network of NPF-500. The efficient EnT process from -bicarbazole to porphyrin in NPF-500-HTCPP was captured by time-resolved spectroscopy and exemplified by photocatalytic oxidation of thioanisole. These results demonstrate not only the capability of NPF-500 as the scaffold to precisely arrange the donor-acceptor assembly for the EnT process but also the potential to directly utilize the EnT process for photocatalytic applications.
在过去的几十年中,人们已经尝试了很多次来模拟光合作用中的能量转移(EnT),这是自然界中发生的一个关键过程,对太阳能燃料和可持续能源具有根本意义。金属-有机骨架(MOFs)是一种新兴的多孔晶体材料,由有机连接体和金属或金属簇节点自组装而成,为探索定向 EnT 现象提供了理想的平台。然而,要在同一个框架中以原子精度放置能量供体和受体部分似乎是一个重大的合成挑战。在这项工作中,我们报告了一种高度多孔和光活性的基于 -咔唑和卟啉的混合配体 MOF 的设计和合成,即 NPF-500-HTCPP(NPF = 内布拉斯加州多孔骨架;HTCPP = -四(4-羧基苯基)卟啉),其中辅助配体 HTCPP 通过 NPF-500 的(4,8)连接网络的八面体笼赤道平面上的开放金属位精确地掺入。NPF-500-HTCPP 中从 -咔唑到卟啉的高效 EnT 过程通过时间分辨光谱捕获,并通过硫代茴香醚的光催化氧化进行了例证。这些结果不仅证明了 NPF-500 作为支架精确排列供体-受体组装以进行 EnT 过程的能力,而且还证明了直接利用 EnT 过程进行光催化应用的潜力。