High resolution solid state NMR in paramagnetic metal-organic frameworks

被引:5
|
作者
Klug, C. A. [1 ]
Swift, M. W. [2 ]
Miller, J. B. [1 ]
Lyons, J. L. [2 ]
Albert, A. [1 ]
Laskoski, M. [1 ]
Hangarter, C. M. [1 ]
机构
[1] US Naval Res Lab, Chem Div, Washington, DC 20375 USA
[2] US Naval Res Lab, Mat Sci Div, Washington, DC USA
关键词
MOF; ZIF-67; NMR; Paramagnetic; Contact shift; Dipole -dipole shift; PROTON RELAXATION-TIMES; SPECTROSCOPY; ADSORPTION; ENERGY; COMPUTATION; ZIF-67; C-13;
D O I
10.1016/j.ssnmr.2022.101811
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We study the metal-organic framework (MOF) ZIF-67 with 1H and 13C nuclear magnetic resonance (NMR). In addition to the usual orbital chemical shifts, we observe spinning sideband manifolds in the NMR spectrum due to hyperfine interactions of the paramagnetic cobalt with 1H and 13C. Both orbital and paramagnetic chemical shifts are in good agreement with values calculated from first principles, allowing high-confidence assignment of the observed peaks to specific sites within the MOF. Our measured resonance shifts, line shapes, and spin lattice relaxation rates are also consistent with calculated values. We show that molecules in the pores of the MOF can exhibit high-resolution NMR spectra with fast spin lattice relaxation rates due to dipole-dipole couplings to the Co2+ nodes in the ZIF-67 lattice, showcasing NMR spectroscopy as a powerful tool for identification and characterization of "guests" that may be hosted by the MOF in electrochemical and catalytic applications.
引用
收藏
页数:8
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