Bulletin of the Chemical Society of Japan p. 447 - 454 (1985)
Update date:2022-08-04
Topics:
Takagi, Shigeru
Miyamoto, T. Ken
Sasaki, Yukiyoshi
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 porphyrin; 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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Doi:10.1021/jo00217a017
(1985)Doi:10.1246/cl.1981.641
(1981)Doi:10.1039/jr9640002128
(1964)Doi:10.1021/ja00305a012
(1985)Doi:10.1021/om00128a004
(1985)Doi:10.1021/jo01034a057
(1964)
