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An iron(III) complex of a novel tripodal tris-hydroxamate, tris[2-{(N-acetyl-N-hydroxy)glycylamino}ethyl]amine (TAGE), was synthesized as a siderophore model. Its X-ray structure revealed that intra- and interstrand hydrogen bonding networks cause an increase in the iron redox potential.
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Matsumoto et al. (2000) studied this question.
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