Lanthanide complexes with pyridine-2,6-dicarboxylic acid: synthesis, crystal structure, thermal and magnetic properties of [LnPDA)2(PDAH2)] · (DMAH2)2(DMAH0.5)2
- 作者: Sharif S.1, Khan B.1, Şahin O.2, Khan I.U.1
-
隶属关系:
- Department of Chemistry
- Sinop University, Scientific and Technological Research Application and Research Center
- 期: 卷 42, 编号 1 (2016)
- 页面: 56-65
- 栏目: Article
- URL: https://journals.rcsi.science/1070-3284/article/view/213369
- DOI: https://doi.org/10.1134/S1070328416010048
- ID: 213369
如何引用文章
详细
Mild solvothermal synthesis, structures, thermal and magnetic properties of coordination complexes [Ln(PDA)2(PDAH2)] · (DMAH2)2(DMAH0.5)2(I–IV) (PDA = pyrdine-2,6-dicarboxylate anion, DMAH = dimethylamine, Ln = Ce, Nd, Sm, and Ho) are described. The DMAH molecules in I–IV, generated in situ from hydrolysis of N,N-dimethylformamide, are responsible to assemble three dimensional coordination polymers through N–H···O and C–H···O hydrogen bonds. Distorted tricapped trigonal prismatic LnO6N3 geometry having 14 triangular faces is attributed to mean deviation of dihedral angles while nitrogen shows fairly triangular faces having dihedral angle close to 60°C (CIF files CCDC nos. 872065 (I), 872070 (II), 872069 (III), and 872066 (IV)). Curie–Weiss law and the overall magnetic behavior are typical for the presence of antiferromagnetic exchange coupling interactions between lanthanide. Thermal decomposition analyses reveal removal of ammonia and resultant complexes showthermal stability. Complexes have been further characterized by using elemental analyzer and FT-IR spectroscopy.
作者简介
S. Sharif
Department of Chemistry
编辑信件的主要联系方式.
Email: msshariflcwu@gmail.com
巴基斯坦, LahoreJail Road Lahore, 54000
B. Khan
Department of Chemistry
Email: msshariflcwu@gmail.com
巴基斯坦, LahoreJail Road Lahore, 54000
O. Şahin
Sinop University, Scientific and Technological Research Application and Research Center
Email: msshariflcwu@gmail.com
土耳其, Sinop, 57010
I. Khan
Department of Chemistry
Email: msshariflcwu@gmail.com
巴基斯坦, Lahore, 54000
补充文件
