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The nature of Mn(II) complexes in concentrated aqueous ammonium oxalate solutions
Author(s) -
MielniczekBrzóska E.
Publication year - 2010
Publication title -
crystal research and technology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.377
H-Index - 64
eISSN - 1521-4079
pISSN - 0232-1300
DOI - 10.1002/crat.201000377
Subject(s) - oxalate , ammonium oxalate , chemistry , manganese , aqueous solution , ligand (biochemistry) , ammonium , impurity , decomposition , inorganic chemistry , ultraviolet , coordination sphere , genetic algorithm , metal , materials science , receptor , organic chemistry , biochemistry , optoelectronics , evolutionary biology , biology
The paper presents an analysis of the results of spectroscopic studies obtained in the ultraviolet range UV for unsaturated ammonium oxalate solutions containing Mn(II) impurity c i . The aim is to follow manganese oxalate formation processes at different ammonium oxalate concentrations c and Mn(II) impurity c i and also to establish how concentrations of particular species change with a change of ratio ( c i / c ). Spectroscopic analysis is discussed from the standpoint of speciation of these complexes in the abovementioned solutions. The coordination of C 2 O 4 2– ligand with Mn(H 2 O) 6 2+ aquacomplex in the range ‐2 < ln( c i / c ) < 1.5 leads to the formation of Mn(C 2 O 4 ) and Mn(C 2 O 4 ) 2 2– complexes, but the coordination of the C 2 O 4 2– ligand with Mn(C 2 O 4 ) 2 2– complex in the concentration ratio range ‐5 < ln( c i / c ) < ‐2 results in the formation of predominantly Mn(C 2 O 4 ) 3 4– complex. The effect of successive coordination of the C 2 O 4 2– ligand is well‐defined in the ultraviolet spectral region. (© 2010 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)
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