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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
Main Authors: 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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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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1520-510X
language eng
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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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