化学
异烟酰胺
结晶学
晶体结构
氢键
分子
反离子
齿合度
红外光谱学
分子间力
离子
单晶
无机化学
有机化学
作者
Brina Dojer,Amalija Golobič,Nejc Babič,Zvonko Jagličić,Matjaž Kristl
标识
DOI:10.1016/j.molstruc.2022.133393
摘要
Two new mononuclear complexes of iron(II) pyridinecarboxamides (picolinamide - pia, isonicotinamide - isn), [Fe(pia)3]·(SO4)·3H2O (1) and (isnH)2[Fe(isn)2(SO4)2(H2O)2]·H2O (2) have been synthesized by the reaction of iron(II) sulphate heptahydrate and pyridinecarboxamides in different solvents by standard method under reflux. Both compounds were characterized by single-crystal X-ray diffraction structure analysis, magnetic measurements and by FT-IR spectroscopy. In the complex cation of 1 Fe2+ ion is six coordinated by three nitrogen and three oxygen atoms from three bidentate picolinamide ligands in mer mode. In complex anion of 2 central Fe2+ ion is six coordinated by two isonicotinamide ligands, two sulphate ligands and two water molecules in trans mode. In both structures complex ions are connected with counterions and crystal water molecules with intermolecular hydrogen bonds. Magnetic properties of the compounds were measured between 2 K and 300 K giving the results: µeff = 4.5 BM for compound 1 and µeff = 4.7 BM for 2. Experimental values of the IR spectra are comparable with literature data and are in good agreement with results of the structural analysis.
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