We have acquired 1H and 13C solid-state NMR (ssNMR) spectra of the paramagnetic Cu(II)-2-pyrazine-carboxylate (Cu-Py) complex and assigned paramagnetic 1H/13C signals using density functional theory (DFT) calculations. The unpaired electron in Cu(II) ionexacerbates the 1H and 13C chemical shifts in the Cu-Py complex through hyperfine interactions, making the conventional NMR signal assignment non-feasible. Further, the nuclear fast relaxation in paramagnetic metal-organic system hampers application of routine ssNMR techniques for signal acquisition. In our work we have employed simple DEPTH experiment at 50 kHz magic angle spinning (MAS) for acquiring 1H and 13C 1D ssNMR spectra of the paramagnetic Cu(II)-2-pyrazine-carboxylate (Cu-Py) complex. The paramagnetic augmented (diamagnetic chemical shift + paramagnetic shift) 1D 1H and 13C ssNMR signals (shifts) from Cu-Py complex have major contribution from Fermi contact interaction due to proximity of the organic arm to Cu2+ ion (Cu2+-C/H atoms 0-5 Å). The unpaired electron spin density distributed over the pyrazine-carboxylate organic arm is crucial in understanding Fermi contact shifts and hence accounts for 1H and 13C ssNMR signal assignment. The theoretical Fermi contact shifts together with diamagnetic shifts, calculated using density functional theory (DFT) at B3LYP level with basis sets viz. 6-311G, 6-311G+(D) and 6-311G++(D), were compared with the experimental shifts to facilitate the process of signal assignment. Vibrational analysis of Cu-Py complex was performed at B3LYP level of theory with various basis sets in comparison with experimental IR data. This further assisted in double validation of DFT optimized Cu-Py structure used here for extracting Fermi contact shifts. Furthermore molecular orbital analysis on the DFT optimized Cu-Py structure articulates the spin density distribution mechanism, thereby stipulating the location of the unpaired electron in the Cu(II) dx
2
-y
2 orbital in Paramagnetic Cu-Py complex.
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