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In a saddle conformation, the pyrrole rings are tipped alternately above and below the mean plane of the porphyrin and the meso carbons remain in or nearly in plane. In a ruffled geometry (vide infra), the pyrrole rings twist so that the b carbons lie above and below the core plane as do the meso carbons [45].
-
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53
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+ complexes has recently been shown [10] to affect their EPR properties and model the 'large g max' EPR signals of some protein bound, histidine-ligated cytochromes.
-
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54
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z2 occupancy, the Ni-N distances to the imidazoles observed here are certainly consonant with a high spin Ni(II) [35].
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