Mn(II)三吡唑硼酸盐配合物Mn[HB(pz)3]2和Mn[HB(3,5‐Me2‐pz)3]2的合成和结构

Y. Xing, K. Aoki, F. Bai
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引用次数: 7

摘要

摘要Mn(OOCCH3)2分别与NaHB(pz)3和NaHB(3,5‐Me2‐pz)3在MeOH中反应得到Mn(II)配合物Mn[HB(pz)3]2 (1) (pz =吡唑)和Mn[HB(3,5‐Me2‐pz)3]2(2)。两个配合物(1)和(2)通过红外光谱、元素分析和x射线衍射进行了表征。配合物(1)在C2/c空间群中结晶,a = 18.971(3) Å, b = 13.700(3) Å, c = 19.056(3) Å, β = 111.378(10), V = 4612.0(13) Å3, Z = 2。配合物(2)在空间群R‐3中结晶,a = 10.9832(18) Å, b = 10.983(2) Å, c = 24.785(3) Å, γ = 120°,V = 2589.3(7) Å3, Z = 3。X射线结构分析表明,配合物(1)和(2)均为单体中性配合物,在金属Mn中心周围具有相似的配位模式。此外,还讨论了相关的键距、键角和结构性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis and Structure of the Mn(II) Complexes with Tripyrazolylborate Ligands: Mn[HB(pz)3]2 and Mn[HB(3,5‐Me2‐pz)3]2
Abstract Mn(II) complexes Mn[HB(pz)3]2 (1) (pz = pyrazole) and Mn[HB(3,5‐Me2‐pz)3]2 (2) have been obtained by the reaction of Mn(OOCCH3)2 with NaHB(pz)3 and NaHB(3,5‐Me2‐pz)3 in MeOH, respectively. The two complexes (1) and (2) were characterized by IR, elemental analyses, and x‐ray diffraction. Complex (1) crystallizes in the space group C2/c, a = 18.971(3) Å, b = 13.700(3) Å, c = 19.056(3) Å, β = 111.378(10), V = 4612.0(13) Å3, Z = 2. Complex (2) crystallizes in the space group R‐3, a = 10.9832(18) Å, b = 10.983(2) Å, c = 24.785(3) Å, γ = 120°, V = 2589.3(7) Å3, Z = 3. X‐ray structure analysis has shown that the complexes (1) and (2) all are monomeric neutral complexes, and possess similar coordination modes around the metal Mn centers. In addition, some related bonding distances, angles, and structural properties are discussed.
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