Abstract

Reacting Mn(ClO4)2·6H2O and H2phpzEt (H2phpzEt=5(3)-(2-hydroxyphenyl)-3(5)-ethylpyrazole) in methanol in the presence of sodium hydroxide yields the compound [Mn2(HphpzEt)4(H2O)2](ClO4)2 (1). The pentanuclear [Mn5(μ3-O)2(HphpzEt)3(phpzEt)3(OCH3)(HOCH3)2(O2CPh)] (2) is obtained when performing a similar reaction with Mn(O2CPh)2·2H2O. Compound 1 consists of a symmetric dinuclear manganese(III) cationic unit, [Mn2(HphpzEt)4(H2O)2]2+ with two non-coordinated perchlorate anions. Compound 2 is a rare pentanuclear complex containing all the manganese ions in the oxidation state III and it also has μ3-oxido ligands. Temperature- and field-dependent magnetization studies indicate dominant antiferromagnetic interactions between the manganese(III) ions in both compounds.

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