One- and two-dimensional cobalt benzenecarboxylate coordination polymers containing a kinked organodiimine: Synthesis, structure, and magnetic properties

被引:13
作者
Johnston, Lindsey L.
Brown, Kyalarnboka A.
Martin, David P.
LaDuca, Robert L. [1 ]
机构
[1] Michigan State Univ, Lyman Briggs Coll, E Lansing, MI 48825 USA
关键词
coordination polymer; cobalt; dipyridylamine; benzoate; phenylacetate; antiferromagnetism;
D O I
10.1016/j.molstruc.2007.09.014
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hydrothermal reaction of cobalt nitrate, phenylmalonic acid, and 4,4'-dipyridylamine (dpa) resulted in formation of the coordination polymer [Co-2(phaC)(4)(dPa)(2)(H2O)] (1, phac = phenylacetate), where the phac ligand is formed in situ by the decarboxylation of phenylmalonic acid. Binuclear [Co-2(phaC)(4)(H(2)0)] units with both bridging and monodentate benzenecarboxylate ligands are linked into a two-dimensional (4,4) rhomboid grid network via dpa tethers within the structure of 1. Use of benzoate as the anionic component allowed the formation of [Co(benzoate)(2)(dpa)(2)] (2), which manifested a dpa-linked one-dimensional chain coordination polymer motif with pendant monodentate and chelating carboxylates. Modest antiferromagnetic coupling was observed within the binuclear units in 1. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:80 / 87
页数:8
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