Solid-state NMR spectroscopy at ultrahigh resolution for structural and dynamical studies of MOFs

IF 1.7
Qing Wang , Min Peng , Cong-Cong Liang , Jing Tan , Sophia Zhang , Yue-Biao Zhang , Haiming Liu
{"title":"Solid-state NMR spectroscopy at ultrahigh resolution for structural and dynamical studies of MOFs","authors":"Qing Wang ,&nbsp;Min Peng ,&nbsp;Cong-Cong Liang ,&nbsp;Jing Tan ,&nbsp;Sophia Zhang ,&nbsp;Yue-Biao Zhang ,&nbsp;Haiming Liu","doi":"10.1016/j.mrl.2023.02.002","DOIUrl":null,"url":null,"abstract":"<div><p>To characterize the structure and dynamics of metal–-organic frameworks (MOFs) in-depth at the molecular level, it is necessary to pursue high-resolution solid-state magic angle spinning (MAS) nuclear magnetic resonance (NMR) spectroscopy. Spectral resolution is usually affected by the quality of materials and various experimental conditions, of which magic angle (MA) accuracy is a crucial determinant. The current industrial criteria for MA calibration based on the common standard of KBr were found insufficient in guaranteeing optimal resolution MAS NMR for highly ordered MOFs. To drive towards higher-resolution MAS NMR spectroscopy, we propose a calibration protocol for more accurate MA with a higher-precision criterion based on <sup>79</sup>Br MAS NMR of KBr, where the linewidth ratio of the fifth-order spinning sideband to the central band of KBr should be less than 1.00. As a result, ultrahigh-resolution <sup>13</sup>C cross-polarization (CP) MAS NMR of MOF-5 is achieved with minimal linewidths as low as 4 Hz, and therefore MOF-5 can be used as a new standard convenient for verifying MA accuracy and also optimizing <sup>13</sup>C CP conditions. Maintaining high-precision MA under variable temperature (VT) was found challenging on certain commercial MAS NMR probes, as was systematically investigated by VT NMR using KBr and MOF-5. Nevertheless, ultrahigh-resolution MAS NMR spectroscopy with stable MA under VT is employed to reveal fine structures and linker dynamics of a series of Zn-based MOFs with highly regulated structures. The ultrahigh-resolution NMR methodcan be generally applied to study a broad range of MOFs and other materials.</p></div>","PeriodicalId":93594,"journal":{"name":"Magnetic Resonance Letters","volume":"3 2","pages":"Pages 175-186"},"PeriodicalIF":1.7000,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Magnetic Resonance Letters","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772516223000128","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

To characterize the structure and dynamics of metal–-organic frameworks (MOFs) in-depth at the molecular level, it is necessary to pursue high-resolution solid-state magic angle spinning (MAS) nuclear magnetic resonance (NMR) spectroscopy. Spectral resolution is usually affected by the quality of materials and various experimental conditions, of which magic angle (MA) accuracy is a crucial determinant. The current industrial criteria for MA calibration based on the common standard of KBr were found insufficient in guaranteeing optimal resolution MAS NMR for highly ordered MOFs. To drive towards higher-resolution MAS NMR spectroscopy, we propose a calibration protocol for more accurate MA with a higher-precision criterion based on 79Br MAS NMR of KBr, where the linewidth ratio of the fifth-order spinning sideband to the central band of KBr should be less than 1.00. As a result, ultrahigh-resolution 13C cross-polarization (CP) MAS NMR of MOF-5 is achieved with minimal linewidths as low as 4 Hz, and therefore MOF-5 can be used as a new standard convenient for verifying MA accuracy and also optimizing 13C CP conditions. Maintaining high-precision MA under variable temperature (VT) was found challenging on certain commercial MAS NMR probes, as was systematically investigated by VT NMR using KBr and MOF-5. Nevertheless, ultrahigh-resolution MAS NMR spectroscopy with stable MA under VT is employed to reveal fine structures and linker dynamics of a series of Zn-based MOFs with highly regulated structures. The ultrahigh-resolution NMR methodcan be generally applied to study a broad range of MOFs and other materials.

Abstract Image

用于MOFs结构和动力学研究的超高分辨率固态NMR光谱
为了在分子水平上深入表征金属有机骨架(mof)的结构和动力学,有必要采用高分辨率固态魔角旋转(MAS)核磁共振(NMR)波谱技术。光谱分辨率通常受到材料质量和各种实验条件的影响,其中魔角精度是决定光谱分辨率的关键因素。目前基于KBr通用标准的MA校准工业标准不足以保证高有序mof的最佳分辨率MAS NMR。为了推动更高分辨率的MAS核磁共振光谱,我们提出了一种基于KBr的79Br MAS核磁共振的更高精度标准的更精确的MA校准方案,其中KBr的五阶自旋边带与中心带的线宽比应小于1.00。结果表明,MOF-5在最小线宽低至4 Hz的情况下实现了超高分辨率13C交叉极化(CP) MAS NMR,因此MOF-5可以作为便于验证MA精度和优化13C CP条件的新标准。在使用KBr和MOF-5进行的VT NMR系统研究中,某些商用MAS NMR探针在变温度(VT)下保持高精度MA是一项挑战。然而,采用在VT下具有稳定MA的超高分辨率MAS NMR谱,揭示了一系列具有高度调节结构的锌基mof的精细结构和连接动力学。超高分辨率核磁共振方法可广泛应用于mof和其他材料的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Magnetic Resonance Letters
Magnetic Resonance Letters Analytical Chemistry, Spectroscopy, Radiology and Imaging, Biochemistry, Genetics and Molecular Biology (General)
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信