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NMR chemical shifts of urea loaded copper benzoate. A joint solid-state NMR and DFT study

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Abstract

We report solid-state 13C NMR spectra of urea-loaded copper benzoate, Cu2(C6H5CO2)4.2(urea), a simplified model for copper paddlewheel-based metal-organic frameworks (MOFs), along with first-principles density functional theory (DFT) computation of the paramagnetic NMR (pNMR) chemical shifts. Assuming a Boltzmann distribution between a diamagnetic open-shell singlet ground state (in a broken-symmetry Kohn-Sham DFT description) and an excited triplet state, the observed δ(13C) values are reproduced reasonably well at the PBE0-⅓/IGLO-II//PBE0-D3/AE1 level. Using the proposed assignments of the signals, the mean absolute deviation between computed and observed 13C chemical shifts is below 30 ppm over a range of more than 1100 ppm.
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Original languageEnglish
JournalSolid State Nuclear Magnetic Resonance
VolumeIn press
Early online date20 Apr 2019
DOIs
Publication statusE-pub ahead of print - 20 Apr 2019

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