期刊
SYNTHESIS AND REACTIVITY IN INORGANIC AND METAL-ORGANIC CHEMISTRY
卷 33, 期 5, 页码 817-836出版社
MARCEL DEKKER INC
DOI: 10.1081/SIM-120021648
关键词
N-(o-vanillinidene)-p-anisidine; N,N '-bis(o-vanillinidene)-ethylenediamine; Cu(II); Co(II); Mn(II); Ni(II); Zn(II); Sm(III); Th(IV); UO2(VI) complexes
Two Schiff bases, N-(o-vanillinidene)-p-anisidine (o-VPAH) and N,N'-bis(o-vanillinidene)ethylenediamine (o-VEDH2), and eleven complexes of the compositions [M(L)(OAc)(H2O)] {where M = Cu(II) (1), Co(II) (2), Mn(II) (3) or Ni(II) (4) and OAcH = CH3COOH}, [Zn(L)(2)].H2O (5), [M(L')(H2O)(2)] {where M = Cu(II) (6) or Ni(H) (7)}, [Zn(L')].2H(2)O (8), [Sm(L')(OAc)(H2O)] (9), [Th(L')(NO3)(2)] (10) and [UO2(L')(H2O)] H2O(11)(where LH = o-VPAH, and L'H-2, = o-VEDH2), were prepared. From the elemental analyses, IR, electronic and NMR spectra, magnetic susceptibility measurements and thermal studies, the mode of chelation of the ligands and geometry of the complex molecules were assigned. In all of the complexes, o-VPAH acts as a monobasic-bidentate ligand and o-VEDH2 acts as a dibasic-tetradentate ligand. The presence of water is revealed by thermograms and supported by the presence of relevant hands in their IR spectra. Suitable structures have been proposed for these complexes.
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