首页> 外文期刊>Journal of the Chemical Society, Dalton Transactions. Inorganic Chemistry >Effects of metal co-ordination geometry on self-assembly: a monomeric complex with trigonal prismatic metal co-ordination vs. tetrameric complexes with octahedral metal co-ordination
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Effects of metal co-ordination geometry on self-assembly: a monomeric complex with trigonal prismatic metal co-ordination vs. tetrameric complexes with octahedral metal co-ordination

机译:金属配位几何形状对自组装的影响:具有三角棱柱形金属配位的单体配合物与具有八面体金属配位的四聚体配合物

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Complexes of Mn~(II), Co~(II) and Zn~(II) with the hexadentate podand ligand tris [3, (2-pyridyl) pyrazol-1-yl] hydroborate [L]~- have been prepared and structurally characterised. In mononuclear [CoL][PF_6] centre dot CH_2Cl_2 all three bidentate arms of the ligand are co-ordinated to the Co~(II) in a relatively strain-free manner to give a trigonal prismatic co-ordination geometry. In contrast in [Mn_4L_4][PF_6]_4 centre dot 4MeCN centre dot Et_2O and [Zn_4L_4][PF_6]_3[OH] centre dot 12EtOH the [M_4L_4]~(4+) complex cations are tetrahedral clusters. Each ligand [L]~- co-ordinates one bidentate arm to each of three metal ions in a #kappa#~2: #kappa#~2: #kappa#~2 co-ordination mode, such that each ligand caps one triangular face of the metal tetrahedron. This trinucleating co-ordination mode, and the 1:1 correspondence of octahedral metal ions and hexadentate ligands, necessarily results in formation of the tetrahedral cluster in which all four metal tris (chelate) centres have the same chirality. Thus the mononucleating #kappa#~6 co-ordination mode results when the metal ion can tolerate a trigonal prismatic geometry, whereas the trinucleating #kappa#~2: #kappa#~2: #kappa#~2 mode occurs when the metal ions are octahedral. Spectroscopic evidence (~1H NMR and UV/VIS spectroscopy and electrospray mass spectrometry, as appropriate) suggests that the monomeric and tetrameric forms are retained in solution and do not interconvert. Attempts to recrystallise [Zn_4L_4][PF_6]_4 from acetone-diethyl ether resulted in formation of a few crystals of the decomposition product [Zn_4L_4](pypz)_2(#mu#_4-PO_4)[PF_6]_3 centre dot 2Me_2CO centre dot 2Et_2O [pypz = 3-(2-pyridyl)pyrazole], in which [L]~- adopts the hitherto unseen binucleating (#kappa#~4: #kappa#~2) co-ordination mode, the central bridging phosphate arising from hydrolysis of [PF_6]~- under ambient conditions.
机译:制备了Mn〜(II),Co〜(II)和Zn〜(II)与六齿豆荚配体三[3,(2-吡啶基)吡唑-1-基]氢硼酸盐[L]〜-的配合物,并在结构上表征。在单核[CoL] [PF_6]中心点CH_2Cl_2中,配体的所有三个双齿臂均以相对无应变的方式与Co〜(II)配位,从而形成了三角棱柱形配位几何。相反,在[Mn_4L_4] [PF_6] _4中心点4MeCN中心点Et_2O和[Zn_4L_4] [PF_6] _3 [OH]中心点12EtOH中,[M_4L_4]〜(4+)络合物阳离子是四面体簇。每个配体[L]〜-在#kappa#〜2:#kappa#〜2:#kappa#〜2配位模式下,将一个双齿臂与三个金属离子中的每一个配位,使得每个配体的顶角为一个三角形金属四面体的表面。这种三核配位模式以及八面体金属离子和六齿配体的1:1对应关系必然导致四面体簇的形成,其中所有四个金属三(螯合物)中心都具有相同的手性。因此,当金属离子可以容忍三角棱柱几何形状时,将产生单核#kappa ~~ 6配位模式,而当金属离子出现时,将出现三核#kappa#〜2:#kappa#〜2:#kappa#〜2模式。是八面体的。光谱学证据(约1H NMR和UV / VIS光谱以及电喷雾质谱法)表明,单体和四聚体形式保留在溶液中,并且不会相互转化。尝试从丙酮-乙醚中重结晶[Zn_4L_4] [PF_6] _4导致形成分解产物[Zn_4L_4](pypz)_2(#mu#_4-PO_4)[PF_6] _3中心点2Me_2CO中心点的一些晶体2Et_2O [pypz = 3-(2-吡啶基)吡唑],其中[L]〜-采用迄今未见的双核配位(#kappa#〜4:#kappa#〜2)配位模式,中央桥接的磷酸盐由[PF_6]〜-在环境条件下的水解。

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