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Syntheses, structural studies and solution properties of iron complexes of some amide-substituted calixarenes

机译:某些酰胺取代的杯芳烃的铁配合物的合成,结构研究和溶液性质

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Iron(III) complexes of 5,11,17,23-tetra-tert-butyl-24-hydroxy-26,27,28-tris(diethylcarbamoylmetho xy) calix[4] arene (II) and 5,11,17,23,29,35-hexa-tert-butyl-36,39-dihydroxy-37,38,40,41-tetrakis(diet hylcarbamoylmethoxy) calix[6] arene (IV) have been synthesised, and a single crystal structure determination has been carried out on [Fe(II - H)] (FeCl4)(2); the iron in the complex cation is bound to all seven O atoms of the calixarene with the shortest Fe-O distance to the phenolate O atom. The voltammetric properties of these complexes and the previously described Fe(III) complex of 5,11,17,23-tetra-tert-butyl-25,27-dihydroxy-26,28-bis(diethylcarbamoylmeth oxy) calix[4] arene (I) have been studied. The results suggest that the complexes of I and II undergo a reduction which is metal-centred, and an oxidation which is ligand-centred. [References: 27]
机译:5,11,17,23-四叔丁基-24-羟基-26,27,28-三(二乙基氨基甲酰基甲氧基xy)杯[4]芳烃(II)和5,11,17的铁(III)络合物合成了23,29,35-六叔丁基-36,39-二羟基-37,38,40,41-四(对苯二甲酸氨基甲酰基甲氧基)杯[6]芳烃(IV),确定了单晶结构在[Fe(II-H)](FeCl4)(2)上进行;络合阳离子中的铁与杯芳烃的所有七个O原子键合,而Fe-O与酚盐O原子的距离最短。这些配合物和先前描述的5,11,17,23-四叔丁基-25,27-二羟基-26,28-双(二​​乙基氨基甲酰基甲基氧基)杯[4]芳烃的Fe(III)配合物的伏安特性(一)已研究。结果表明,I和II的配合物经历了以金属为中心的还原和以配体为中心的氧化。 [参考:27]

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