Precise Structural and Dynamical Details in Zeolites Revealed by Coupling-Edited 1 H- 17 O Double Resonance NMR Spectroscopy

• Published in: Journal of the American Chemical Society
• Main Authors: Ji, Yi, Chen, Kuizhi, Han, Xiuwen, Bao, Xinhe, Hou, Guangjin
• Format: Journal Article
• Language: English
• Published: United States 25-03-2024
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/jacs.3c14787

Despite the extensive industrial and research interests in zeolites, their intrinsic catalytic nature is not fully understood due to the complexity of the hydroxyl-aluminum moieties.
O NMR would provide irreplaceable opportunities for much-needed fine structural determination given the ubiquitous presence of oxygen atoms in nearly all species; however, the low sensitivity and quadrupolar nature of oxygen-17 make its NMR spectroscopic elucidation challenging. Here, we show that state-of-the-art double resonance solid-state NMR techniques have been combined with spectral editing methods based on scalar (through-bond) and dipolar (through-space) couplings, which allowed us to address the subtle protonic structures in zeolites. Notably, the often-neglected and undesired second-order quadrupolar-dipolar cross-term interaction ("2nd-QD interaction") can actually be exploited and can help gain invaluable information. Eventually, a comprehensive set of
H-
O/
H-
Al double resonance NMR with
-/
-coupling spectral editing techniques have been designed in this work and enabled us to reveal atomic-scale precise structural and dynamical details in zeolites including: 1) The jump rate of the bridging acid site (BAS) proton is relatively low, i.e., far less than 100 s
at room temperature. 2) The Al-OH groups with
H chemical shift at 2.6-2.8 ppm, at least for nonseverely dealuminated H-ZSM-5 catalysts, exhibit a rigid bridging environment similar to that of BAS. 3) The Si-OH groups at 2.0 ppm are not hydrogen bonded and undergo fast cone-rotational motion. The results in this study predict the 2nd-QD interaction to be universal for any rigid -
O-H environment, such as those in metal oxide surfaces or biomaterials.