Abstract
Abstract A new model compound “tulip garden” porphyrin, has a long half-lifetime, thus satisfying the demand for the synthetic analogue of myoglobin. At the same time, “tulip garden” porphyrin has high O2 affinities as compared to other protected porphyrins; especially, its Co(II) complex shows almost the same affinity (P1/2O2) as coboglobins. The difference in oxygen affinities between “tulip garden” and “picket fence-type” porphyrins can be ascribed to the bulkiness of pendant groups. The strong “side” influence of the adamantyl group can be expected to bring about a high O2 affinity.
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