首页> 外文期刊>Inorganica Chimica Acta >Pyridine-2,6-dicarboxylate and perchlorate bridged hydrogen bonded 1D chains involving manganese(Ill)-cyclam moiety: synthesis, X-ray crystal structures and magnetic study
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Pyridine-2,6-dicarboxylate and perchlorate bridged hydrogen bonded 1D chains involving manganese(Ill)-cyclam moiety: synthesis, X-ray crystal structures and magnetic study

机译:吡啶-2,6-二羧酸盐和高氯酸盐桥连的氢键连接的一维链,涉及锰(III)-环素部分:合成,X射线晶体结构和磁性研究

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Two compounds H[Mn(cyclam)(pyridine-2,6-dicarboxylate)(2)](H2O)-H-. (1) and [Mn-III(cyclam)Cl-2]ClO4 (2) (where cyclam = 1,4,8,11-tetraazacyclotetradecane) have been synthesized and structurally characterized. The complex I crystallizes in the monoclinic space group P2(1)/c with a = 11.4328(11), b = 14.4275(14), c = 8.5782(9) Angstrom, V = 1343.1(2) Angstrom(3), Z = 2, R = 0.0453. Complex 1 is octahedral in which [Mn(cyclam)](3+) unit occupies the basal plane having two pyridine-2,6-dicarboxylate anions in the axial positions. Molecular packing of the crystal is dominated by string of molecules along the b-axis. The strings are held together by extensive intermolecular hydrogen bonds involving N-(HO)-O-..., N-(HN)-N-... and O-(HO)-O-... which impart it an infinite 1D chain. Complex 2 on the other hand crystallizes in the space group P2(1)2(1)2(1) (No. 19) of the orthorhombic system. Mn(III) ions occupy the center of a distorted octahedron and two chloride ions occupy the axial positions. The packing diagram of 2 reveals that the complex is percholrate-bridged hydrogen bonded ID chain along a-axis. Cyclic voltammogram of complex 1 shows a reduction wave at -0.25 V coupled to an oxidation wave at -0.05 V versus SCE in aqueous solution. The complex 2 is characterized by an irreversible reduction wave at -0.11 V versus SCE and is identical to that observed for [Mn-III(cyclam)Cl-2]Cl(.)5H(2)O. The magnetic measurements in the temperature range 1.9-300 K have been carried out for complex 1 which exhibits a very weak ferromagnetic interaction at low temperature. Complex 2 shows room temperature magnetic moment value of 4.92 BM consistent with the high spin d(4) electronic configuration. (C) 2003 Elsevier B.V. All rights reserved. [References: 47]
机译:两种化合物H [Mn(cyclam)(吡啶-2,6-二羧酸吡啶)(2)](H2O)-H-。 (1)和[Mn-III(cyclam)Cl-2] ClO4(2)(其中cyclam = 1、4、8、11-四氮杂环十四烷)已经合成并在结构上表征。复合物I在单斜空间群P2(1)/ c中结晶,其中a = 11.4328(11),b = 14.4275(14),c = 8.5782(9)埃,V = 1343.1(2)埃(3),Z = 2,R = 0.0453。配合物1是八面体,其中[Mn(cyclam)](3+)单元占据在轴向上具有两个吡啶-2,6-二羧酸根阴离子的基面。晶体的分子堆积由沿b轴的一串分子控制。弦通过广泛的分子间氢键连接在一起,这些氢键涉及N-(HO)-O -...,N-(HN)-N -...和O-(HO)-O -...无限一维链。另一方面,络合物2在正交晶系的空间群P2(1)2(1)2(1)(19号)中结晶。 Mn(III)离子占据扭曲的八面体的中心,而两个氯离子占据轴向位置。 2的堆积图表明,该络合物是沿a轴的高氯酸盐桥连的氢键ID链。配合物1的循环伏安图显示-0.25 V的还原波与-0.05 V的氧化波相对于水溶液中的SCE。配合物2的特征是相对于SCE在-0.11 V下具有不可逆还原波,并且与[Mn-III(cyclam)Cl-2] Cl(。)5H(2)O观察到的还原波相同。对于在低温下表现出非常弱的铁磁相互作用的配合物1,已经在1.9-300K的温度范围内进行了磁性测量。配合物2显示的室温磁矩值为4.92 BM,与高自旋d(4)电子配置一致。 (C)2003 Elsevier B.V.保留所有权利。 [参考:47]

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