Syntheses, crystal structures and properties of new manganese(II) complexes with macrocyclic polyamine ligands bearing pyridyl donor pendants
摘要:
Two new Mn-II complexes with polydentate macrocyclic polyamine ligands functionalized with pyridyl donor pendants, 1,4,7,10-tetrakis(2-pyridylmethyl)-1,4,7,10-tetraazacyclododecane (L-1) and 1-methly-4,7,10-tris(2-pyridylmethyl)-1,4,7, 10-tetraazacyclododecane (L-2), have been synthesized and their structures determined by X-ray diffraction analysis. In [MnL1](ClO4)(2) (I), the Mn-II central ion is eight-coordinated with all the eight donor nitrogens of L-1 (including four pendant pyridyl nitrogens and four tertiary amines of cyclen) to form a distorted square-prism coordination geometry, and in [MnL2](ClO4)(2) (II), the M-II central ion is seven-coordinated (distorted monocapped octahedral geometry) with all the seven nitrogen donor atoms of L2 (including three pendant pyridyl nitrogens and four tertiary amines of cyclen) comprising the donor set. The solution chemistry of the two Mn-II complexes has been further studied by cyclic voltammetry (CV), W-Vis and ESR spectral techniques. (C) 2000 Elsevier Science Ltd. All rights reserved.
The present invention relates to a method of generating chlorine dioxide from chlorite salts in the presence of an iron ion-containing complex, a method of treating a substrate with a chlorine-containing oxidant in the presence of an iron ion-containing complex and related aqueous media, kits and compositions.
The first seven-coordinated iron(II) complex with a nitrogen donor set hepta-dentate macrocyclic polyamine ligand and different coordination modes with its cobalt(II) analogue
The Fe2+ and Co2+ complexes with a hepta-dentate ligand, 1-methyl-4,7,10-tris(2-pyridylmethyl)-1,4,7,10-tetraazacyclododecane (L), have been synthesized and their crystal structures determined by X-ray diffraction analyses. The two complexes have been found to have different coordination modes. The Fe2+ complex (I) is seven-coordinated with the four cyclen (cyclen = 1,4,7,10-tetraazacyclododecane) nitrogen donors and all three pendant pyridine nitrogens, adopting a mono-capped distorted octahedral coordination geometry. To our knowledge, this is the first example of a structurally characterized seven-coordinated Fe2+ complex formed with only one N-7 done; set ligand. Whereas the Co2+ complex (TI) of L is a normal six-coordination with four cyclen nitrogen donors and two pendant pyridines to give a distorted octahedron in which one pendant pyridine nitrogen remains uncoordinated. (C) 2000 Elsevier Science B.V. All rights reserved.