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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Synthesis of mixed-valence hexanuclear Mn(II/III) clusters from its Mn(II) precursor: variations of catecholase-like activity and magnetic coupling
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Synthesis of mixed-valence hexanuclear Mn(II/III) clusters from its Mn(II) precursor: variations of catecholase-like activity and magnetic coupling

机译:从其Mn(II)前体合成混合价六核Mn(II / III)簇:儿茶酚酶样活性和磁耦合的变化

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One Mn(II) coordination polymer, [Mn(o-(NO2)C6H4COO)(2)(pyz)(H2O)](n) (1), has been synthesized and oxidized with n-Bu4NMnO4 in non-aqueous media to two mixed-valence hexanuclear Mn(II/III) complexes [(Mn2Mn4O2)-Mn-III-O-II(pyz)(0.61)/(MeOH)(0.39)(o-(NO2)C6H4COO)(10)center dot(H2O)center dot{(CH3)(2)CO}(2)]center dot(CH3)(2)CO (2) and [(Mn2Mn4O2)-Mn-III-O-II- pyz)(0.28)/(MeCN)(3.72)(o-(NO2)C6H4COO)(10)center dot(H2O)] (3) (where pyz = pyrazine). All three complexes were characterized by elemental analyses, IR spectroscopy, single-crystal X-ray diffraction analyses, and variable-temperature magnetic measurements. The structural analyses reveal that complex 1 is comprised of linear chains of pyz bridged Mn(II), which are further linked to one another by syn-anti carboxylate bridges, giving rise to a two-dimensional (2D) net. Complexes 2 and 3 feature mixed valence [(Mn2Mn4II)-Mn-III] units in which each of the six manganese centres reside in an octahedral environment. Apart from the variations in terminal ligands (acetone for 2 and acetonitrile for 3), the complexes are very similar. Using 3,5-di-tert-butyl catechol (3,5-DTBC) as the substrate, the catecholase-like activity of the complexes has been studied and it is found that the mixed valent Mn-6 complexes (2 and 3) are much more active towards aerial oxidation of catechol compared to the Mn(II) complex (1). Variable-temperature (1.8-300 K) magnetic susceptibility measurements showed the presence of antiferromagnetic coupling in all three complexes. The magnetic data have been fitted with a 2D quadratic model derived by Lines, giving the exchange constant J/k(B) = -0.0788(5) K for 1. For 2 and 3, antiferromagnetic interactions within the Mn6 cluster have been fitted with models containing three exchange constants: J(A)/k(B) = -70 K, J(B)/k(B) = -0.5 K, J(C)/k(B) = -2.9 K for 2 and J(A)/k(B) = -60 K, J(B)/k(B) = -0.3 K, J(C)/k(B) = -2.8 K for 3.
机译:一种Mn(II)配位聚合物[Mn(o-(NO2)C6H4COO)(2)(pyz)(H2O)](n)(1)已合成,并在非水介质中用n-Bu4NMnO4氧化,得到两个混合价六核Mn(II / III)配合物[(Mn2Mn4O2-Mn-III-O-II(pyz)(0.61)/(MeOH)(0.39)(o-(NO2)C6H4COO)(10)中心点(H2O)中心点{(CH3)(2)CO}(2)]中心点(CH3)(2)CO(2)和[(Mn2Mn4O2)-Mn-III-O-II-pyz)(0.28)/ (MeCN)(3.72)(邻-(NO2)C6H4COO)(10)中心点(H2O)](3)(其中pyz =吡嗪)。通过元素分析,红外光谱,单晶X射线衍射分析和变温磁测量对这三种复合物进行了表征。结构分析表明,配合物1由pyz桥接的Mn(II)线性链组成,这些链通过顺-反羧酸酯桥彼此进一步连接,从而形成二维(2D)网络。配合物2和3具有混合价[(Mn2Mn4II)-Mn-III]单元,其中六个锰中心均位于八面体环境中。除了末端配体的变化(丙酮为2,乙腈为3)外,配合物非常相似。以3,5-二叔丁基邻苯二酚(3,5-DTBC)为底物,研究了配合物的儿茶酚酶样活性,发现混合价的Mn-6配合物(2和3)与Mn(II)配合物(1)相比,对儿茶酚的空气氧化活性更高。可变温度(1.8-300 K)的磁化率测量表明,所有三个复合物中均存在反铁磁耦合。磁数据已用Lines推导的2D二次模型拟合,给出了1的交换常数J / k(B)= -0.0788(5)K。对于2和3,已拟合了Mn6团簇内的反铁磁相互作用包含三个交换常数的模型:J(A)/ k(B)= -70 K,J(B)/ k(B)= -0.5 K,J(C)/ k(B)= -2.9 K对于2和对于3,J(A)/ k(B)= -60 K,J(B)/ k(B)= -0.3 K,J(C)/ k(B)= -2.8 K

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