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Amide Coupling Reaction for the Synthesis of Bispyridine-based Ligands and Their Complexation to Platinum as Dinuclear Anticancer Agents
Published on: May 28, 2014
Dodenuclear [Mn(III)(8)Ln(III)(4)] clusters with 2-(hydroxymethyl)pyridine: syntheses, structures, and magnetic
Lei Sun1, Hui Chen, Chengbing Ma
1State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, The Chinese Academy of Sciences, Fuzhou, Fujian 350002, China. ccn@fjirsm.ac.cn.
Abstract:
A new family of isostructural Mn/Ln dodenuclear clusters: [Mn8Ln4(O)8(hmp)4(O2CPh)12(NO3)4(PhCO2H)(C2H5OH)] [Ln = La (1), Pr (2), Nd (3), Gd (4), Dy(5), hmpH = 2-(hydroxymethyl)pyridine] have been synthesized by the reaction of Mn(NO3)2 and Ln(NO3)3·6H2O with hmpH and benzoic acid as co-ligands. Compounds 1-5 possess a spindle-shaped core of [MnLn(μ4-O)4(μ3-O)4(μ3-OR)2(μ2-OR)8](10+), which is composed of six face-sharing defected cubane units and two square-pyramidal units. The compounds represent the highest nuclearity Mn/Ln clusters with the use of hmpH to date. That the ferromagnetic interactions dominated within complexes 1-4 were suggested by solid-state dc magnetic susceptibility analyses. Compound 4 displays a magnetic-caloric effect (MCE) with 13.94 J kg(-1) K(-1) as the entropy change at 6 K for ΔH = 8 T. Compounds 1 and 5 exhibit an out-of-phase χ''M peak maximum above 2.0 K. Fitting of the ac susceptibility data to an Arrhenius law gives an energy barrier Ueff = 6.88/7.44 K for compounds 1 and 5 respectively.
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