Manganese, cobalt, nickel and zinc complexes with pyrazine-2-carboxylic acid.

IF 1.2 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Saša Petriček
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引用次数: 0

Abstract

New complexes of zinc (1), manganese(II) (2 and 2a), cobalt(II) (3) and nickel(II) chloride (4), with pyzaH (pyrazine-2-carboxylic acid) were synthesized. The pyzaH molecules are coordinated as monodentate ligands only through heterocyclic nitrogen in 1, 2 and 3, as shown by single crystal X-ray diffraction analysis. The chloride ions are coordinated as terminal ligands in 1, [ZnCl2(pyzaH)2]×2H2O, but act as bridging ligands in the 1D complexes [MCl2(pyzaH)2]n×2nH2O (M = Mn, 2, Co, 3). The supramolecular architectures of the complexes differ due to the coordination of the chlorides, the hydrogen bonds and the parallel stacking arrangements of the pyzaH molecules. In contrast to the isolated crystals of 1, 2 and 3, the manganese(II) (2a) and nickel(II) (4), compounds do not contain water.  According to the IR spectra and the results of thermal analyzes, the proposed formula is [MCl2(pyzaH)2]. Powder X-ray and thermal analysis results demonstrate the isostructural nature of complexes 2a and 4. The low thermal stability of 1 is due to the monodentate coordination of pyzaH in 1. Thermal decomposition of 1, 2a and 4 in air produces oxides MO (M = Mn, Ni, Zn).

锰、钴、镍和锌与吡嗪-2-羧酸配合物。
合成了锌(1)、锰(II)(2和2a)、钴(II)(3)和氯化镍(II)(4)与吡嗪-2-羧酸(pyzaH)配合物。单晶x射线衍射分析表明,pyzaH分子仅通过杂环氮在1、2和3上配位为单齿配体。氯离子在1,[ZnCl2(pyzaH)2]×2H2O中作为末端配体,但在1D配合物[MCl2(pyzaH)2]n×2nH2O中作为桥接配体(M = Mn, 2, Co, 3)。配合物的超分子结构因氯化物的配位、氢键的配位和pyzaH分子的平行堆叠排列而不同。与1、2和3的分离晶体相反,锰(II) (2a)和镍(II)(4)的化合物不含水。根据红外光谱和热分析结果,提出的公式为[MCl2(pyzaH)2]。粉末x射线和热分析结果证实了配合物2a和4的同工结构性质。1的低热稳定性是由于pyzaH在1中的单齿配位。1,2a和4在空气中热分解产生氧化物MO (M = Mn, Ni, Zn)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta Chimica Slovenica
Acta Chimica Slovenica 化学-化学综合
CiteScore
2.50
自引率
25.00%
发文量
80
审稿时长
1.0 months
期刊介绍: Is an international, peer-reviewed and Open Access journal. It provides a forum for the publication of original scientific research in all fields of chemistry and closely related areas. Reviews, feature, scientific and technical articles, and short communications are welcome.
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