期刊
JOURNAL OF SOLID STATE CHEMISTRY
卷 212, 期 -, 页码 141-146出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jssc.2014.01.018
关键词
Cobalt(II)-organic framework; Acylamide; Tetracarboxylate ligand; Gas adsorption; Magnetic property
资金
- National Nature Science Foundation of China [21001061]
- Liaocheng University Fund for Younger Scientist [31805]
A new cobalt(II)-organic framework, [Co-2(L)(py)(2)(DMSO)](n)center dot 0.5nDMF center dot 2nDMSO (1) [H4L=5,5'-((naphthalene-2,6-dicarbonyl)bis(azanediyl))diisophthalic acid, py=pyridine, DMSO=dimethyl sulfoxide, DMF=N,N-dimethylformamide], has been solvothermally synthesized and characterized by elemental analysis, IR, TGA, PXRD and single-crystal X-ray crystallography. The structural analysis reveals that complex 1 is a 3D framework built from nanosized acylamide-containing tetracarboxylate ligands (L4-) and dinuclear [Co-2(CO2)(4)] secondary building units (SBUs), exhibiting a uninodal (4,4)-connected crb topology with the Schlafli symbol of (4.6(5)). The desolvated complex (1a) displays higher adsorption capability for CO2 than N-2, which may be due to the relatively strong binding affinity between the CO2 molecules and acylamide groups in the framework. The magnetic investigation shows that the dominant antiferromagnetic interaction is observed in complex 1. (C) 2014 Elsevier Inc. All rights reserved.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据