Abstract

In this contribution we present a continuous wave (CW), pulse electron paramagnetic resonance (EPR), and pulse electron nuclear double resonance (ENDOR) study of (OEC)Co(C6H5), where OEC is the trianion of 2,3,7,8,12,13,17,18-octaethylcorrole. To facilitate spectral assignments isotopic substitutions were employed (2H and 13C). From the analysis of the frozen solution CW EPR, ESEEM, and ENDOR spectra measured at X- and Q-band, we determined the electronic coupling parameters of the unpaired electron with the cobalt nucleus, corrole nitrogen nuclei, phenyl 13C, 1H and 2H nuclei, meso 1H and 2H nuclei, and ethyl 1H nuclei. Determination of the g matrix alignment in the molecular frame was achieved by successfully simulating the orientationally selective powder ENDOR spectra of the meso nuclei. The g principal values are g1 = 1.9670, g2 = 2.1122, and g3=2.0043, with the g1 and g2 axes pointing at the nitrogens of the corrole macrocycle and the g3 axis directed perpendicular to the plane. The cobalt hyperfine...

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