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首页> 外文期刊>New Journal of Chemistry >Dinuclear cobalt(III) and mixed valence trinuclear Mn-III-Mn-II-Mn-III complexes with a tripodal bridging pyridylaminophenol ligand
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Dinuclear cobalt(III) and mixed valence trinuclear Mn-III-Mn-II-Mn-III complexes with a tripodal bridging pyridylaminophenol ligand

机译:三核桥接吡啶基氨基酚配体的双核钴(III)和混合价三核Mn-III-Mn-II-Mn-III配合物

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A dinuclear cobalt(II), [Co2(kappa(4)-O,O', N,N'-L)(2)(mu-O,O'-HCOO)](ClO4)center dot(C2H5)(2)O (1) and a linear mixed valence trinuclear manganese, [Mn-3(kappa(4)-O,O', N,N'-L)(2)(mu-CH3O)(2)(mu-O,O'-CH3COO)(2)]center dot 2(C2H5)(2)O (2) complexes with the ligand N-(2-pyridyl-methyl)-N, N-bis-[2'-hydroxy-5'-methyl-benzyl]-amine (H2L) are reported. For both complexes the ligand is present in the deprotonated form. The coordination sphere of the cobalt centres can be described as slightly distorted octahedral with two bridging O-phenoxo, one N-pyridine, one N-amine, one terminal O-phenoxo and one bridging O-formate donor atoms. Interestingly, the bridging formate resulted from the aerial oxidation of methanol. The manganese complex (2) has a linear mixed valence Mn-III-Mn-II-Mn-III, with the Mn-II and Mn-III centres bridged by alkoxo, carboxylate and phenoxo groups. Cyclic voltammetry studies show both metal and ligand centred redox processes consistent with the structure of the complexes. Complex (2) has an S = 3/2 ground state; magnetic susceptibility measurements indicate a weak antiferromagnetic interaction. The best fit of the magnetic susceptibility data as a function of temperature was obtained using a conventional trinuclear linear model [H = -2J(S1S2 + S1S3)] with J = -0.79 cm(-1) and g = 1.99.
机译:双核钴(II),[Co2(kappa(4)-O,O',N,N'-L)(2)(mu-O,O'-HCOO)](ClO4)中心点(C2H5)( 2)O(1)和线性混合价三核锰[Mn-3(kappa(4)-O,O',N,N'-L)(2)(mu-CH3O)(2)(mu- O,O'-CH3COO)(2)]中心点2(C2H5)(2)O(2)与配体N-(2-吡啶基-甲基)-N,N-双-[2'-羟基-报道了5'-甲基-苄基]-胺(H 2 L)。对于两种复合物,配体均以去质子化形式存在。钴中心的配位体可描述为八面体轻微扭曲的八面体,具有两个桥接的O-苯氧,一个N-吡啶,一个N-胺,一个末端的O-苯氧和一个桥接的O-甲酸酯供体原子。有趣的是,桥接甲酸盐是由甲醇的空气氧化产生的。锰配合物(2)具有线性混合价Mn-III-Mn-II-Mn-III,其中Mn-II和Mn-III中心由烷氧基,羧酸根和苯氧基桥接。循环伏安法研究表明,以金属和配体为中心的氧化还原过程均与配合物的结构一致。复数(2)的S = 3/2基态;磁化率测量表明反铁磁相互作用弱。使用常规三核线性模型[H = -2J(S1S2 + S1S3)],J = -0.79 cm(-1),g = 1.99,可获得磁化率数据随温度变化的最佳拟合。

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