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首页> 外文期刊>Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry >Synthesis and investigation of biologically active complexes of N-alkylphenothiazines with yttrium(III)
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Synthesis and investigation of biologically active complexes of N-alkylphenothiazines with yttrium(III)

机译:N-烷基吩噻嗪与钇的生物活性复合物的合成和研究

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New complexes of yttrium(III) with six N-alkylphenothiazines having the formula [Y(L)(2)(NO3)(2)]NO3, (L = N-alklylphenothiazines) have been prepared and characterized by analytical, conductance, IR, UV-visible add NMR spectral studies. Conductance studies indicate the 1:1 electrolytic behavior of the nitrate complexes. The IR spectra of the complexes show that all N-alkylphenothiazines act as bidentate ligands, the heterocyclic nitrogen and the tertiary nitrogen atom of the side chain being the sites of coordination. Only two of the nitrate group are coordinated bidentately to tile central metal ion, while the third remains uncoordinated. The fungitoxicity of the complexes against several fungi has been assayed. [References: 18]
机译:制备了钇(III)与六种具有化学式[Y(L)(2)(NO3)(2)] NO3(L = N-烷基吩噻嗪)的N-烷基吩噻嗪的新配合物,并通过分析,电导,IR对其进行了表征,紫外可见添加NMR光谱研究。电导研究表明硝酸盐配合物的1:1电解行为。配合物的IR光谱表明,所有的N-烷基吩噻嗪都充当二齿配体,侧链的杂环氮和叔氮原子是配位点。硝酸盐基团中只有两个与中心金属离子发生了二齿配位,而第三个则保持不配位。已经测定了该复合物对几种真菌的真菌毒性。 [参考:18]

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