Yi Xianfeng, Xiao Yao, Xia Changjiu, Liu Fengqing, Liu Yujia, Hui Yu, Yu Xin, Qin Yucai, Chen Wei, Liu Zhiqiang, Song Lijuan, Zheng Anmin
State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, National Center for Magnetic Resonance in Wuhan, Wuhan Institute of Physics and Mathematics, Innovation Academy for Precision Measurement Science and Technology, Chinese Academy of Sciences, Wuhan 430071, China.
University of Chinese Academy of Sciences, Beijing 100049, China.
Fundam Res. 2023 Jan 7;5(1):174-182. doi: 10.1016/j.fmre.2022.12.015. eCollection 2025 Jan.
Elucidating the nature of the active sites in heterogeneous catalysts is fundamental for understanding their reactivity and catalytic performances. Although stannosilicate zeolites have tremendous application potential for catalyzing biomass-related compounds in aqueous media, the detailed local structures and features of the real active sites and their possible structural variations under reaction conditions are poorly understood to date. In this study, a dynamic transformation of framework Sn-O-Si sites to Sn-OH/Si-OH pairs and subsequently a pseudo-Brønsted acid in stannosilicate zeolites upon molecular adsorption, which is analogous to various adsorbates/reactants under working conditions, was identified by solid-state nuclear magnetic resonance (NMR) spectroscopy for the first time, which challenges the widespread assumption that the active center structures remain rigid/stable during the catalytic process. These results provide new comprehensive insights for the fundamental understanding of the dynamic and flexible active centers and involved reaction mechanisms of novel zeolite catalysts with heterometal atoms, such as Sn, Ti, and Zr.
阐明多相催化剂中活性位点的性质对于理解其反应活性和催化性能至关重要。尽管锡硅沸石在催化水相介质中与生物质相关的化合物方面具有巨大的应用潜力,但迄今为止,人们对实际活性位点的详细局部结构和特征以及它们在反应条件下可能的结构变化了解甚少。在本研究中,首次通过固态核磁共振(NMR)光谱法确定了在分子吸附时,锡硅沸石中骨架Sn-O-Si位点动态转变为Sn-OH/Si-OH对,随后形成类似工作条件下各种吸附质/反应物的准布朗斯特酸,这对广泛认为活性中心结构在催化过程中保持刚性/稳定的假设提出了挑战。这些结果为深入理解具有异金属原子(如Sn、Ti和Zr)的新型沸石催化剂的动态灵活活性中心及相关反应机理提供了新的全面见解。