2006
DOI: 10.1007/s10967-006-0231-5
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Mössbauer studies on the thermolysis of manganese tris(malonato)ferrate(III)hexahydrate

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Cited by 4 publications
(9 citation statements)
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“…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: 92%
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“…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: 92%
“…As a result, a bidentate coordination could be assigned to Fe(III) ions. A sharp and distinct band at 566 cm -1 ascertains the bonding of Fe(III) to the citrate ligands in octahedral geometry [5,6]. Probably, in the unidentate type of coordination, the ions of Zn(II) and Mg(II) are involved.…”
Section: Ftir-studymentioning
confidence: 99%
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