2001
DOI: 10.1016/s0277-5387(00)00636-7
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Novel dinuclear manganese(III) complexes with bi- or tridentate and bridging tetradentate Schiff base ligands: preparation, properties and catalase-like function

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Cited by 23 publications
(17 citation statements)
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“…All this suggests the interaction of hydrogen peroxide with central Mn III atoms. The observed changes in 300–430 nm is similar to that reported earlier by Nakamura et al42b and Moreno et al12a for Mn III complexes.…”
Section: Resultssupporting
confidence: 91%
“…All this suggests the interaction of hydrogen peroxide with central Mn III atoms. The observed changes in 300–430 nm is similar to that reported earlier by Nakamura et al42b and Moreno et al12a for Mn III complexes.…”
Section: Resultssupporting
confidence: 91%
“…As can be observed in Figure 1 the donor atoms N1, N22 and O10 occupy one face of the octahedron while N4, N42 and O30 occupy the other face. The axial Mn-N pyridine bond distances of 2.248(6) and 2.282(6) Å in complex 1 are the longest of the coordination sphere and this is consistent with a Jahn- [28][29][30][32][33][34] The trans angles at the Mn III center in 1 are in the range of 168.7(2)-173.7(2)° with the greatest distortion from linearity occurring at the O10-Mn-O4 and O30-Mn-N1 angles.…”
Section: Description Of the Crystal Structures Of Complexes 1 Andsupporting
confidence: 67%
“…Mn LMCT upon reaction with H 2 O 2 can be interpreted taking into account the effect of the carboxylate binding mode on the spectroscopic properties of these complexes. If upon reaction with H 2 O 2 , the bridging acetato shifts to a monodentate coordinated acetato, it should function as a weaker donor and should reduce the energy gap between the d p and PhO p orbitals thus causing a red shift of the signal [50][51][52]. Besides, the shift of the bridging methanolato ligand to a weakly bound terminal ligand should also contribute to the red shift of the band.…”
Section: Discussionmentioning
confidence: 99%