Dinuclear dimethoxolized iron(III)-L-proline complexes, obtained as a result of thermal, photolytic, and chemoreductive rearrangement of trinuclear oxobridged iron(III)-L-proline complexes, have been characterized by spectral and magnetic measurements. Under the conditions described, the rearrangement does not occur in other solvents nor when parallel complexes with other L-amino acids are used, including, surprisingly, L-hydroxyproline.
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Rita Asplund (1981) studied this question.
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