Manganese(II)-promoted ligand oxidation during the formation of a coordination polymer

被引:5
作者
Su, Zhao [1 ]
Yue, Qi [1 ]
Yi, Xiu-Chun [1 ]
Wang, Kun [1 ]
Gao, En-Qing [1 ]
机构
[1] E China Normal Univ, Shanghai Key Lab Green Chem & Chem Proc, Dept Chem, Shanghai 200062, Peoples R China
基金
高等学校博士学科点专项科研基金; 美国国家科学基金会;
关键词
Carboxylate; Coordination polymer; In situ oxidation; Magnetic properties; Manganese; METAL-ORGANIC FRAMEWORK; MAGNETIC-PROPERTIES; CRYSTAL-STRUCTURES; X-RAY; TRINUCLEAR; COMPLEXES; CLUSTERS; COPPER(I); MONONUCLEAR; TOPOLOGY;
D O I
10.1016/j.inoche.2013.03.034
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
During the synthesis of Mn(II) compounds from fluorene-2,7-dicarboxylate, the ligand undergoes in situ oxidation to generate a Mn(II) coordination polymer with the ligand fluorenone-2,7-dicarboxylate (FODC2-). It was demonstrated that the transformation occurs with dioxygen as reactant and Mn(II) as catalyst. The resulting coordination polymer, [Mn-3(FODC)(3)(DMA)(4)]center dot 2.5DMA, displays a 2D network based on the [Mn-3(COO)(6)(DMA)(4)] unit with triple carboxylate bridges. Magnetic analyses were performed not only on temperature-variable susceptibility but also on field-variable magnetization, indicating weak antiferromagnetic interactions through the triple bridges. (c) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:129 / 132
页数:4
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