Wang Xinchao, Wang Zhiwen, Wang Zhaoxing, Liu Tian-Fu, Li Shangda, Wang Fei, Zhang Jian
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian, 350002, P. R. China.
Adv Sci (Weinh). 2025 Jan;12(2):e2412592. doi: 10.1002/advs.202412592. Epub 2024 Nov 19.
Utilizing ultrathin 2D metal-organic framework nanosheets (2D MONs) as supports for incorporating chiral catalysts represents a highly promising avenue in the field of asymmetric catalysis. In this study, four pairs of isostructural chiral metal-organic layers (MOLs) adorned with N-Heterocyclic carbene (NHC) groups are successfully synthesized. Notably, the obtained bulky (S)-1-Zn crystals can be readily delaminated into ultrathin MONs consisting of 1-2 layers through an ion intercalation-assisted exfoliation process. Subsequent asymmetric catalysis studies revealed that the NHC sites can be effectively activated by a proton sponge while maintaining structural integrity for the subsequent benzoin condensation. Due to their well-exposed catalytic sites, ultrathin morphology, and porous structure, the (S)-1-Zn nanosheets exhibited significantly enhanced yield and enantioselectivity compared to their bulk counterparts and organic precursors. This research highlights an efficient strategy for incorporating chiral NHC species onto 2D MONs, thereby unlocking their immense potential for heterogeneous asymmetric catalysis.
利用超薄二维金属有机框架纳米片(2D MONs)作为负载手性催化剂的载体,在不对称催化领域是一条极具前景的途径。在本研究中,成功合成了四对装饰有N-杂环卡宾(NHC)基团的同构手性金属有机层(MOLs)。值得注意的是,通过离子插层辅助剥离过程,所获得的块状(S)-1-Zn晶体可以很容易地剥离成由1-2层组成的超薄MONs。随后的不对称催化研究表明,质子海绵可以有效地激活NHC位点,同时保持结构完整性以进行后续的安息香缩合反应。由于其暴露良好的催化位点、超薄形态和多孔结构,(S)-1-Zn纳米片与其块状对应物和有机前体相比,产率和对映选择性显著提高。这项研究突出了一种将手性NHC物种负载到二维MONs上的有效策略,从而释放了它们在多相不对称催化中的巨大潜力。