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- W2003128972 abstract "During the past five years, hybrid density functional theory has been used to study mechanisms for redox-active enzymes containing complexes with a variety of different transition metals. In this paper, suggested mechanisms of some manganese enzymes are described. For photosystem II, a mechanism is proposed leading to an oxyl radical in the S(3)-state, which is the precursor for the O-O bond formation. For manganese catalase, the suggested mechanism instead leads to the formation of a hydroxyl radical after the O-O bond of hydrogen peroxide is cleaved. This radical is immediately quenched by a manganese center. Parallels between these enzymes are highlighted. Jahn-Teller and trans effects are emphasized." @default.
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- W2003128972 date "2002-04-01" @default.
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- W2003128972 title "Quantum chemical studies of manganese centers in biology" @default.
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- W2003128972 doi "https://doi.org/10.1016/s1367-5931(02)00312-5" @default.
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