2000
DOI: 10.1023/a:1009225701332
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Abstract: This paper briefly presents a review concerning the species which can arise when iron salts and citric acid are mixed together. The data commented on are required for a correct interpretation of the chemical processes which play a paramount role in biology and in the biological studies involving iron-citrate complexes.

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Cited by 102 publications
(64 citation statements)
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“…The reported binding stoichiometries for ATP, ADP, and citrate to Fe(III) show a surprising variation, ranging from 1:2 (55) to 1:6 (56) for Fe(III)-ATP and from 1:1 to 1:4 for the Fe(III)-citrate complex, for example (57). Consequently, the binding stoichiometries and thus the chemical characteristics of the Fe(III) complexes under the present experimental conditions are undefined.…”
Section: Effect Of Lipoyl Dehydrogenase On the Epr-detectable Signal mentioning
confidence: 99%
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“…The reported binding stoichiometries for ATP, ADP, and citrate to Fe(III) show a surprising variation, ranging from 1:2 (55) to 1:6 (56) for Fe(III)-ATP and from 1:1 to 1:4 for the Fe(III)-citrate complex, for example (57). Consequently, the binding stoichiometries and thus the chemical characteristics of the Fe(III) complexes under the present experimental conditions are undefined.…”
Section: Effect Of Lipoyl Dehydrogenase On the Epr-detectable Signal mentioning
confidence: 99%
“…ent on the characteristics of the chelating ligand (12,25,40 (25,40,55,57,73,74). Therefore, kinetic properties of the lipoyl dehydrogenase-mediated Fe(III) reduction and NAD(P)H oxidation can be assessed only in the absence of oxygen (see below).…”
Section: Flavoenzyme-mediated Fe(iii) Reductionmentioning
confidence: 99%
“…The frequency shift of the IR-active bands, with respect to the theoretical positions from 3150 to 3213 cm -1 and from1400 to 1437 cm -1 were assigned to formation of hydrogen bonds in the sample "Precursor" with NH 4 + participation [15]. The formation of citrate complexes is proven by the doublets located at 1617 and 1578 cm -1 due to antisymmetric stretching vibration, and at 1415 and 1399 cm -1 due to symmetrical stretching vibration of ionized carboxylate groups [5,6,10,13]. The band positions are close to the ones cited in the analogous citrate precursors for ferrites, which are listed in Table 1.…”
Section: Ftir-studymentioning
confidence: 93%
“…The two bands at 524 and 480 cm -1 were assigned to Zn-O and Mg-O bonds [16,17]. The most common coordination for d 10 cations of Zn is tetrahedral and they mainly form covalent bonds with ligands [18]. For the d° cations of Mg, interactions with ligands are predominantly columbic or ionic, however, the tetrahedral geometry is also characteristic of their complexes [18].…”
Section: Ftir-studymentioning
confidence: 99%
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