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Dioxygen-copper reactivity and functional modeling of hemocyanins. Reversible binding of O2 and CO to dicopper(I) complexes [CuI2(L)]2+ (L = dinucleating ligand) and the structure of a bis(carbonyl) adduct, [CuI2(L)(CO)2]2
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Published in: | Inorganic chemistry 1992-04, Vol.31 (8), p.1436-1451 |
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container_end_page | 1451 |
container_issue | 8 |
container_start_page | 1436 |
container_title | Inorganic chemistry |
container_volume | 31 |
creator | KARLIN, K. D TYEKLAR, Z FAROOQ, A HAKA, M. S GHOSH, P CRUSE, R. W GULTNEH, Y HAYES, J. C TOSCANO, P. J ZUBIETA, J |
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doi_str_mv | 10.1021/ic00034a026 |
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source | ACS CRKN Legacy Archives |
subjects | Bioinorganic chemistry Chemistry Condensed matter: structure, mechanical and thermal properties Exact sciences and technology Inorganic chemistry and origins of life Inorganic compounds Metal complexes Physics Structure of solids and liquids crystallography Structure of specific crystalline solids |
title | Dioxygen-copper reactivity and functional modeling of hemocyanins. Reversible binding of O2 and CO to dicopper(I) complexes [CuI2(L)]2+ (L = dinucleating ligand) and the structure of a bis(carbonyl) adduct, [CuI2(L)(CO)2]2 |
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