Synthesis and Structure of Iron(II) Complexes with 1-Methyl-2-pyridin-2-yl-1H- and 1-Methyl-2-phenyliminomethyl-1H-benzimidazoles and Boron Cluster Anions [BnHn]2– (n = 10, 12)

IF 1.1 3区 化学 Q4 CHEMISTRY, INORGANIC & NUCLEAR
V. V. Avdeeva, A. S. Kubasov, S. E. Nikiforova, O. N. Belousova, E. A. Malinina, N. T. Kuznetsov
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引用次数: 0

Abstract

The study addresses the complex formation reactions between iron(II) and benzimidazole (L) derivatives (L1 = C13N3H11, L2 = C15N3H13) in the presence of boron cluster anion salts [BnHn]2– (n = 10, 12). The prepared complexes [FeL3][BnHn] were characterized by elemental analysis and IR spectroscopy. The structure of [\({\text{FeL}}_{{\text{3}}}^{{\text{1}}}\)][B10H10] was established by single crystal X-ray diffraction (CCDC no. 2432134). The distorted octahedral environment of the Fe atom is formed by the imidazole and pyridine nitrogen atoms of the three ligand molecules. In the crystal, the \({{{\text{[FeL}}_{{\text{3}}}^{{\text{1}}}{\text{]}}}^{{{\text{2 + }}}}}\) complex has a meridional configuration. The Fe–N bond lengths for the imidazole nitrogen atoms are in the 1.954(8)–1.980(6) Å range, while for the pyridine nitrogen atoms, this range is 1.977(7)–2.011(8) Å.

Abstract Image

Abstract Image

1-甲基-2-吡啶-2-基- 1h -和1-甲基-2-苯基-甲基- 1h -苯并咪唑与硼簇阴离子[BnHn]2 - (n = 10,12)配合物的合成与结构
研究了铁(II)与苯并咪唑(L)衍生物(L1 = C13N3H11, L2 = C15N3H13)在硼簇阴离子盐[BnHn]2 - (n = 10,12)存在下的络合生成反应。用元素分析和红外光谱对制备的配合物[FeL3][BnHn]进行了表征。[\({\text{FeL}}_{{\text{3}}}^{{\text{1}}}\)][B10H10]的结构通过单晶x射线衍射(CCDC no。2432134)。铁原子的畸变八面体环境是由三个配体分子的咪唑氮原子和吡啶氮原子形成的。在晶体中,\({{{\text{[FeL}}_{{\text{3}}}^{{\text{1}}}{\text{]}}}^{{{\text{2 + }}}}}\)配合物具有子午构型。咪唑氮原子的Fe-N键长在1.954(8)~ 1.980(6)Å之间,吡啶氮原子的Fe-N键长在1.977(7)~ 2.011(8)Å之间。
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来源期刊
Russian Journal of Coordination Chemistry
Russian Journal of Coordination Chemistry 化学-无机化学与核化学
CiteScore
2.40
自引率
15.80%
发文量
85
审稿时长
7.2 months
期刊介绍: Russian Journal of Coordination Chemistry is a journal that publishes reviews, original papers, and short communications on all aspects of theoretical and experimental coordination chemistry. Modern coordination chemistry is an interdisciplinary science that makes a bridge between inorganic, organic, physical, analytical, and biological chemistry.
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