Lin Hengyu, Yang Yihao, Diamond Brian G, Yan Tian-Hao, Bakhmutov Vladimir I, Festus Kelechi W, Cai Peiyu, Xiao Zhifeng, Leng Mingwan, Afolabi Ibukun, Day Gregory S, Fang Lei, Hendon Christopher H, Zhou Hong-Cai
Department of Chemistry, Texas A&M University, College Station, Texas 77843, United States.
Department of Chemistry, University of Oregon, Eugene, Oregon 97403, United States.
J Am Chem Soc. 2024 Jan 17;146(2):1491-1500. doi: 10.1021/jacs.3c10917. Epub 2024 Jan 3.
3D metal-organic frameworks (MOFs) have gained attention as heterogeneous photocatalysts due to their porosity and unique host-guest interactions. Despite their potential, MOFs face challenges, such as inefficient mass transport and limited light penetration in photoinduced energy transfer processes. Recent advancements in organic photocatalysis have uncovered a variety of photoactive cores, while their heterogenization remains an underexplored area with great potential to build MOFs. This gap is bridged by incorporating photoactive cores into 2D MOF nanosheets, a process that merges the realms of small-molecule photochemistry and MOF chemistry. This approach results in recyclable heterogeneous photocatalysts that exhibit an improved mass transfer efficiency. This research demonstrates a bottom-up synthetic method for embedding photoactive cores into 2D MOF nanosheets, successfully producing variants such as PCN-641-NS, PCN-643-NS, and PCN-644-NS. The synthetic conditions were systematically studied to optimize the crystallinity and morphology of these 2D MOF nanosheets. Enhanced host-guest interactions in these 2D structures were confirmed through various techniques, particularly solid-state NMR studies. Additionally, the efficiency of photoinduced energy transfer in these nanosheets was evidenced through photoborylation reactions and the generation of reactive oxygen species (ROS).
三维金属有机框架(MOF)因其孔隙率和独特的主客体相互作用而作为多相光催化剂受到关注。尽管具有潜力,但MOF面临着诸如传质效率低下以及在光诱导能量转移过程中光穿透有限等挑战。有机光催化的最新进展发现了多种光活性核,而它们的多相化仍然是一个未被充分探索但构建MOF潜力巨大的领域。通过将光活性核纳入二维MOF纳米片来弥合这一差距,这一过程融合了小分子光化学和MOF化学领域。这种方法产生了可回收的多相光催化剂,其传质效率得到了提高。本研究展示了一种将光活性核嵌入二维MOF纳米片的自下而上的合成方法,成功制备了PCN - 641 - NS、PCN - 643 - NS和PCN - 644 - NS等变体。系统研究了合成条件以优化这些二维MOF纳米片的结晶度和形态。通过各种技术,特别是固态核磁共振研究,证实了这些二维结构中增强的主客体相互作用。此外,通过光硼化反应和活性氧(ROS)的产生证明了这些纳米片中光诱导能量转移的效率。