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Mononuclear Transition Metal Complexes of 7-Nitro-1,3,5-Triazaadamantane

机译:7-硝基-1,3,5-三氮济会的单核过渡金属复合物

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Complexes of the type [MCl2(7-nitro-1,3,5-triaza-adamantane)2] (M = Zn(II), Pd(II), Pt(II)) and [MCl2(H2O)2(7-nitro-1,3,5-triazaadamantane) 2] (M = Mn (II), Co(II), Ni(II)) have been prepared and their structures have been analysed by X-ray crystallography, elemental analysis, IR and solid state ~(13)C and ~(15)N NMR spectroscopy, supported by density functional theory/ gauge independent atomic orbital (DFT/GIAO) calculations. In each case, 7-nitro-1,3,5-triazaadamantane acts as a mono-dentate ligand and binds to one metal centre only, in spite of the presence of three equivalent amino nitrogens. In the Co(II) and Ni(II) complexes, a two-dimensional intermolecular hydrogen bonding network between the aqua- and the chloro ligands is established. The uncoordinated amines of the 7-nitro-1,3,5-triaza- adamantane are not involved in any H-bonding, as a result of the exceptionally low basicity of this compound.
机译:[mcl2(7-硝基-1,3,5- triaza-adamantane)2]的复合物(m = Zn(ii),pd(ii),pt(ii))和[mcl2(h2o)2(7) -nitro-1,3,5-三氮济会)2](M = M = MN(II),CO(II),Ni(ii)),已经通过X射线晶体学,IR分析,IR分析了它们的结构 和固态〜(13)C和〜(15)N NMR光谱,并由密度函数理论/仪表独立原子轨道(DFT/ GIAO)计算支持。 在每种情况下,尽管存在三种等效的氨基硝基元,但每种情况下7-硝基-1,3,5-三氮济会充当单齿配体,仅与一个金属中心结合。 在CO(II)和Ni(II)配合物中,建立了水a和氯氯配体之间的二维间分子氢键网络。 由于该化合物的碱性异常低,因此7-硝基-1,3,5-三亚壮三亚壮胺的不协调胺不参与任何H键。

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