Abstract
Diiron complexes of dinucleating ligands have been demonstrated to be good structural and spectroscopic models for the diiron-oxo proteins. Although such complexes show relatively sharp isotropically shifted 1 H NMR resonances due to their fast electronic relaxation rates, detailed assignment of their isotropically shifted 1 H NMR resonances has thus far not been achieved due to the difficulty in esablishing bond connectivities on paramagnetic complexes
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