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   <subfield code="a">Novel homogeneous Salen Mn(III) catalysts synthesized from dialdehyde or diketone with o -aminophenol for catalyzing epoxidation of alkenes</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Donglu Xiong, Zaihui Fu, Sheng Zhong, Xiangfen Jiang, Dulin Yin]</subfield>
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   <subfield code="a">A series of novel non-salicylaldehyde based Salen ligands have been synthesized from the condensation of dialdehyde or diketone with o-aminophenol and the corresponding manganese(III) complexes prepared by further coordination of them with $${\hbox{Mn(OAc)}_{2}\cdot 2\hbox{H}_{2}\hbox{O}}$$ . FT-IR, UV-Vis spectra, chemical analysis and the structure optimized by Hartree-Fork/3-21G+ all indicated that the qualities of these novel Mn complexes were relative to their molecular structures. More specifically, glyoxal based Mn complex 2c, which was similar to the traditional Mn(III)-salicylethylenediamine, had a short carbon chain and non geometrical constraint of the aliphatic bridge in the two o-aminophenol, and its quality was the best when compared to glutaraldehyde, 2,4-pentanedione and 1,3-cyclohexanedione based Salen Mn(III) complexes (3c, 4c and 5c). And it was also the excellent catalyst for the epoxidations of several non-functionalized alkenes with molecular oxygen/sacrificial-isobutyaldehyde, PhI(OAc)2 or H2O2 as oxidant.</subfield>
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