首页> 外文期刊>Phosphorus, Sulfur, and Silicon and the Related Elements >SYNTHESIS AND CHARACTERIZATION OF DIIMINE ADDUCTS oF BIS(N-ALKYL-N-FURFURYLDITHIOCARBAMATO-S,S ')CADMIUM(II): CRYSTAL STRUCTURE OF BIS(N-FURFURYL-N-PROPYLDITHIOCARBAMATO-S,S ')(1,10-PHENANTHROLINE)CADMIUM(II)
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SYNTHESIS AND CHARACTERIZATION OF DIIMINE ADDUCTS oF BIS(N-ALKYL-N-FURFURYLDITHIOCARBAMATO-S,S ')CADMIUM(II): CRYSTAL STRUCTURE OF BIS(N-FURFURYL-N-PROPYLDITHIOCARBAMATO-S,S ')(1,10-PHENANTHROLINE)CADMIUM(II)

机译:BIS(N-烷基-N-呋喃二硫代氨基甲酸-S,S')镉(II)的二亚胺添加剂的合成与表征:BIS(N-呋喃基-N-丙硫代氨基甲酸-S,S')(1,10)的晶体结构邻苯二甲酸)镉(II)

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摘要

A series of homoleptic and heteroleptic complexes: [Cd(fprdtc)(2)] (1), [Cd(fprdtc)(2)(1,10-phen)] (2), [Cd(fprdtc)(2)(2,2'-bipy)] (3), [Cd(bufdtc)(2)] (4), [Cd(bufdtc)(2)(1,10-phen)] (5), and [Cd(bufdtc)(2)(2,2'-bipy)] (6)(where fprdtc = N-furfuryl-N-propyldithiocarbamate; bufdtc = N-butyl-N-furfuryldithiocarbamate) have been prepared and characterized. A single crystal X-ray structural analysis was carried out for 2. Reduction in nu C-N (thioureide) for the heteroleptic complexes (2, 3, 5, and 6) compared to that of homoleptic complexes (1 and 4) is attributed to the change in coordination number from four to six and steric effect exerted by 1,10-phenanthroline and 2,2'-bipyridine. The downfield shift of (NCS2)-C-13 carbon signal for heteroleptic complexes from the chemical shift value of homoleptic complexes is also attributed to the increase in coordination number. Single crystal X-ray structure of 2 indicates that the mononuclear structure of 2 shows symmetric coordination of the dithiocarbamate ligands and a distorted octahedral geometry for cadmium, defined by an N2S4 donor set, results. In this crystal structure, most significant pi-pi interaction is also observed.
机译:一系列同源和异源复合物:[Cd(fprdtc)(2)](1),[Cd(fprdtc)(2)(1,10-phen)](2),[Cd(fprdtc)(2)( 2,2'-bipy)](3),[Cd(bufdtc)(2)](4),[Cd(bufdtc)(2)(1,10-phen)](5)和[Cd(bufdtc )(2)(2,2'-bipy)](6)(其中fprdtc = N-糠基-N-丙基二硫代氨基甲酸酯; bufdtc = N-丁基-N-糠基二硫代氨基甲酸酯)并已进行表征。对2进行了单晶X射线结构分析。与均纯络合物(1和4)相比,杂合络合物(2、3、5和6)的nu CN(硫脲)减少。配位数从4变到6,1,10-菲咯啉和2,2'-联吡啶具有立体效应。杂合配合物的(NCS2)-C-13碳信号从纯合配合物的化学位移值向低位偏移也归因于配位数的增加。 2的单晶X射线结构表明2的单核结构显示了二硫代氨基甲酸酯配体的对称配位和镉的扭曲八面体几何形状(由N2S4供体组定义)。在这种晶体结构中,还观察到最显着的pi-pi相互作用。

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