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Synthetic, spectroscopic, and structural studies on organoimido molybdenum, tungsten, and rhenium phthalocyanines

机译:有机亚氨基钼,钨和rh酞菁的合成,光谱和结构研究

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摘要

Unprecedented imido phthalocyaninato complexes of pentavalent refractory metals [PcM(NR)Cl] (M = Mo, W, Re; R = tBu: 1, 3, 6, Mes: 2, 4, 7 or Ts: 5) have been synthesized by reductive cyclotetramerization of phthalonitrile in the presence of appropriate bis(imido) complexes of Mo, W and Re as templates. While d1 Mo(v) and W(v) species 1-5 show distinctive EPR spectra corresponding to metal centered radicals with hyperfine coupling of two magnetically non-equivalent nitrogen atoms (4 equatorial and 1 axial N), corresponding d~2 Re(v) compounds 6 and 7 are diamagnetic. [PcMo(NtBu)Cl] 1 crystallizes from 1-chloronaphthalene in the tetragonal space group P4. The molecular structure reveals, that the metal center is located above the plane of the equatorial N4 and displaced towards the axial π-donor ligand. Due to the thermodynamic trans effect the Mo-Cl bond trans to the imido group is elongated to about 2.600(2) ?.
机译:五价难熔金属[PcM(NR)Cl](M = Mo,W,Re; R = tBu:1,3,6,Mes:2,4,4,7或Ts:5)的空前的亚氨基酞菁酞菁配合物已通过以下方法合成在适当的Mo,W和Re双(亚氨基)配合物作为模板的情况下,将邻苯二甲腈还原四环化。 d1 Mo(v)和W(v)种类1-5显示出独特的EPR谱,对应于以金属为中心的自由基,具有两个非磁性等效氮原子(4个赤道和1个轴向N)的超精细偶联,对应的d〜2 Re( v)化合物6和7是抗磁性的。 [PcMo(NtBu)Cl] 1在四边形空间群P4 / n中从1-氯萘结晶。分子结构表明,金属中心位于赤道N4平面上方并向轴向π供体配体位移。由于热力学反式作用,Mo-Cl键与亚氨基的反式伸长至约2.600(2)Ω。

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