Abstract
Some new manganese complexes containing tetradentate Schiff -base ligands (H2L) derived from 1-hydroxy-2-naphthaldehyde and aliphatic diamines, H2N(CH2)nNH2[n= 2,3,4, or 10; H2L =NN′-ethylene-, propane-1,3-diyl-, butane-1,4-diyl-, and decane-1, 10-diyl-bis(1-hydroxy-2-naphthylmethyleneimine)], have been synthesised. The structure and reactivity of the manganese(II) complexes critically depends on n. Thus, planar [MnL] are formed for n= 2,4, or 10, but for n= 3 the pseudo-octahedral [MnL(H2O)2] is obtained. These manganese (II) species absorb approximately 0.5 mol O2 per mol of Mn to form dimeric di-µ-oxo manganese (IV) complexes [{MnL(O)}2], but this reaction in NN-dimethylformamide is surprisingly much faster for the complex [MnL(H2O)2] than for the planar species. In addition some manganese(III) complexes [MnL(H2O)] ClO4 have been obtained.
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