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Factors influencing the structural and magnetic properties of octahedral cobalt(II) and iron(II) complexes of terdentate N_3 schiff base ligands

机译:影响八齿N_3席夫碱配体的八面体钴(II)和铁(II)配合物的结构和磁性的因素

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The influence of the length of the linking alkyl spacer and of the presence of either a proton or a methyl group, in four related terdentate N_3 Schiff base ligands, on the structures and properties of the resulting iron(II) and cobalt(II) complexes has been investigated. The four ligands were prepared in situ by condensation of 2-(2-aminoethyl)pyridine or 2-(aminomethyl)pyridine with 2-acetylpyridine (L1 vs, L3) or 2-formylpyridine (L2 vs. L4). Hence they comprised a mixture of a relatively rigid chelate with a 2-iminopyridyl moiety, comparable to bipyridine coordination, and a more flexible chelate containing the -(CH_2)_n- spacer. Four iron(II) complexes, [Fe(L1) _2](BF_4)_2 (1), [Fe(L2)_2](BF _4)_2 (2), [Fe(L3)_2](BF_4)_2 (3), [Fe(L4)_2](BF_4)_2 (4), were obtained whereas only in the case of the two ethylene (i.e. not methylene) spaced ligands could pure cobalt(II) complexes, [Co(L1)_2](BF_4)_2 (5), [Co(L2)_2]-(BF_4)_2 (6), be obtained. The ~1H NMR spectra confirmed that in MeCN 1-4 are diamagnetic whereas 5 and 6 are paramagnetic. X-ray structure determinations of the ethylene-linked complexes, 1, 5 and 6, revealed distorted octahedral geometries due to chelate ring restrictions. The M-N distances were typical for high-spin cobalt(II) (5 and 6) and for low-spin iron(II) (1). The magnetic data on 5 and 6 are typical of those expected for distorted octahedral high-spin d~7 species; fitting attempts have yielded zero-field splitting and low symmetry ligand field parameters. A metal-centred M~(2+/3+) redox wave and ligand-based reduction processes were observed for 1-6 in MeCN. The metal-centred redox potential (Fe: 1 0.59, 2 0.68, 3 0.58, 4 0.70 V; Co: 5 0.03, 6 0.09 V vs. Fc/Fc~+) was influenced much more strongly by the presence of the proton vs. methyl group (Fe: shift of 0.09-0.12 V, Co: shift of 0.06 V) than by the bridging methylene vs. ethylene group (Fe: shift of 0.01-0.02 V).
机译:四个相关的齿状N_3 Schiff碱配体中连接的烷基间隔基的长度以及质子或甲基的存在对所得铁(II)和钴(II)配合物的结构和性能的影响已被调查。通过2-(2-氨基乙基)吡啶或2-(氨基甲基)吡啶与2-乙酰基吡啶(L1对L3)或2-甲酰基吡啶(L2对L4)的缩合原位制备四种配体。因此,它们包括具有与联吡啶配位相当的2-亚氨基吡啶基部分的相对刚性的螯合物和含有-(CH_2)_n-间隔基的更柔韧的螯合物的混合物。四种铁(II)络合物,[Fe(L1)_2](BF_4)_2(1),[Fe(L2)_2](BF _4)_2(2),[Fe(L3)_2](BF_4)_2( 3)获得了[Fe(L4)_2](BF_4)_2(4),而只有在两个乙烯(即不是亚甲基)间隔的配体的情况下,才能生成纯的钴(II)配合物[Co(L1)_2得到[(BF_4)_2(5),[Co(L2)_2]-(BF_4)_2(6)。 〜1H NMR光谱证实MeCN 1-4中是抗磁性的,而5和6是顺磁性的。乙烯连接的配合物1、5和6的X射线结构测定表明,由于螯合环的限制,八面体的几何形状发生了扭曲。 M-N距离对于高旋转钴(II)(5和6)和低旋转铁(II)(1)是典型的。 5和6的磁数据是变形的八面体高自旋d〜7物种的典型磁数据。拟合尝试产生了零场分裂和低对称配体场参数。在MeCN中观察到以金属为中心的M〜(2 + / 3 +)氧化还原波和基于配体的还原过程。质子的存在对金属中心的氧化还原电势(Fe:1 0.59,2 0.68,3 0.58,4 0.70 V; Co:5 0.03,6 0.09 V vs.Fc / Fc〜+)的影响更大。甲基(Fe:位移为0.09-0.12V,Co:位移为0.06V)比通过桥连的亚甲基对亚乙基(Fe:位移为0.01-0.02V)。

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