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Synthesis and characterization of polystyrene-anchored monobasic bidentate Schiff base and its complexes with bi-, tri-, tetra- and hexavalent metal ions
Ist Teil von
Journal of coordination chemistry, 2008-06, Vol.61 (11), p.1788-1796
Ort / Verlag
Taylor & Francis Group
Erscheinungsjahr
2008
Link zum Volltext
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
A new monobasic bidentate ON donor Schiff base PS-LH
2
(where PS-LH
2
= polystyrene-anchored Schiff base obtained by condensation of chloromethylated polystyrene (containing 1.17 mmol of chlorine per gram of resin cross-linked with 2% divinylbenzene), 2-hydroxy-1-naphaldehyde and 4-aminosalicylic acid has been synthesized. PS-LH
2
reacts with metal complexes to form polystyrene-anchored complexes: PS-LHM(CH
3
Coo) · DMF (where M = Cu, Zn, Cd, UO
2
), PS-LHZr(OH)
2
(CH
3
Coo) · 2DMF, PS-LHFeCl
2
· 2DMF, PS-LHM′(CH
3
Coo) · 3DMF (where M′ = Mn and Ni) and PS-LHMoo
2
(acac), where acacH = acetylacetone. The polystyrene-anchored complexes have been characterized by elemental analysis, IR, ESR and magnetic susceptibility measurements. The per cent reaction conversion of PS-LH
2
to polystyrene supported coordination compounds lies between 30-95. Shifts of the azomethine ν(C=N) and phenolic ν(C-O) stretches are indicative of ON donor behaviour of the polystyrene-anchored ligands. The complexes, PS-LHCu(CH
3
Coo) · DMF, PS-LHFecl
2
· 2DMF, PS-LHMn(CH
3
Coo) · 3DMF and PS-LHNi(CH
3
Coo) · 3DMF are paramagnetic, while PS-LHZn(CH
3
Coo) · DMF, PS-LHCd(CH
3
COO) · DMF, PS-LHUo
2
(CH
3
Coo) · DMF, PS-LHZr(OH)
2
(CH
3
COO) · 2DMF and PS-LHMoO
2
(acac) are diamagnetic. The copper(II) complex exhibits a square planar structure, zinc(II) and cadmium(II) complexes have tetrahedral structures, nickel(II), manganese(II), iron(III), dioxomolybdenum(VI) and dioxouranium(VI) complexes have octahedral structure and zirconium(IV) complex is pentagonal bipyramidal.