A NMR spectroscopic study of some monothio-β-diketonate chelates and the corresponding β-diketones with a perfluoroethyl substituent

Manoranjan Das, Daniel T. Haworth
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引用次数: 8

Abstract

The 13C and 19F NMR of nine metal complexes contained perfluoroethylmonothio-β-diketonate ligands are recorded in chloroform-d. The complexes are of the type M[RC(S)CHC(O)C2F5]n where M is of nickel, palladium or cobalt; n is 2 or 3 and R is 2′-thienyl, phenyl or 2′-naphthyl. The 13C-NMR data support a fac-octahedral geometry for the cobalt complex (n=3). The 19F NMR show the chemical shift of the difluoromethylene group to be metal dependent. Correlations between the chemical shifts of the respective carbon resonances are also presented and NMR data for the three corresponding β-diketones, RC(OH) = CHC(O)C2F5, are described.

一些含全氟乙基取代基的单硫代β-二酮酸螯合物及相应的β-二酮的核磁共振光谱研究
在氯仿-d中记录了含全氟乙基单硫-β-二酮酸配体的9种金属配合物的13C和19F NMR。配合物为M[RC(S)CHC(O)C2F5]n型,其中M为镍、钯或钴;n是2或3 R是2 ' -噻吩基,苯基或2 ' -萘基。13C-NMR数据支持钴配合物的面八面体几何结构(n=3)。19F核磁共振表明,二氟乙烯的化学位移依赖于金属。给出了各碳共振的化学位移之间的相关性,并描述了三个相应的β-二酮RC(OH) = CHC(O)C2F5的核磁共振数据。
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