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首页> 外文期刊>Zeitschrift fur Anorganische und Allgemeine Chemie >Oxorhenium(V)- and tricarbonylrhenium(I) complexes with substituted pyrazoles as products of the degradation of hydrotrispyrazolylborates
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Oxorhenium(V)- and tricarbonylrhenium(I) complexes with substituted pyrazoles as products of the degradation of hydrotrispyrazolylborates

机译:氧化or(V)-和三羰基hen(I)与取代的吡唑的配合物,是氢三吡唑基硼酸酯降解的产物

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摘要

Hydrotris(3,5-dimethylpyrazol-l-yl)borate and hydrotris(3 -phenylpyrazol-l-yl)bo rate decompose during reactions with [ReOCl3(PPh3)(2)] and [NEt4](2)[Re(CO)(3)Br-3], respectively. The generated pyrazole ligands form complexes with the rhenium(V) oxo and the rhenium(i) tricarbonyl cores.X-ray crystal structures of the oxo-bridged dimer [Cl(PPh3)(O)Re(mu-O)(mu-Me(2)pz)(2)Re(O)(HMe(2)pz)Cl] (1) and [Re(CO)(3)(HPhpz)(2)(Phpz)] (2) (HMe(2)pz = 3,5-dimethylpyrazole, HPhpz = 3-phenyl-pyrazole) show that the substituted pyrazoles can readily deprotonate and act as monodentate or bridging anionic ligands. Re-N bond lengths between 2.09 and 2.14 Angstrom have been observed for the bridging and between 2.12 and 2.23 Angstrom for the terminal pyrazole ligands.
机译:与[ReOCl3(PPh3)(2)]和[NEt4](2)[Re(CO)的反应期间,氢三(3,5-二甲基吡唑-1-基)硼酸酯和氢三(3-苯基吡唑-1-基)bo速率分解)(3)Br-3]。生成的吡唑配体与the(V)氧代和tri(i)三羰基核形成配合物。氧代桥联二聚体[Cl(PPh3)(O)Re(mu-O)(mu- Me(2)pz)(2)Re(O)(HMe(2)pz)Cl](1)和[Re(CO)(3)(HPhpz)(2)(Phpz)](2)(HMe( 2)pz = 3,5-二甲基吡唑,HPhpz = 3-苯基吡唑)表明取代的吡唑可以容易地去质子化并充当单齿或桥接阴离子配体。对于桥接而言,Re-N键长度在2.09至2.14埃之间,对于末端吡唑配体而言,在2.12至2.23埃之间。

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