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H-1 NMR, spectroscopic and molecular modeling studies on paramagnetic lanthanide(III)-quercetin complexes\ud

机译:顺磁性镧系元素(III) - 槲皮素配合物的H-1 NmR,光谱和分子模拟研究

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摘要

Nine coordinated [Ln(quercetin)(3)]nH(2)O complexes were synthesized in non-aqueous solution (where, n = 0 for Pr, Sm, Gd, Tb, Dy and Ho; n = 3, for La and Nd). The complexes were characterized by elemental analysis, molar conductance, UV-vis spectra, IR spectra, thermal analysis and NMR spectra. The optimized structures of the complexes were obtained by molecular modeling. The complexes behave as non-electrolytes in DMSO. TGA study showed anhydrous nature of the complexes (except La and Nd). The H-1 NMR spectra of lanthanum, praseodymium, neodymium and samarium complexes have been studied in DMSO-d(6). The complexes do not dissociate in DMSO and retain their coordination number. The NMR spectra of paramagnetic and diamagnetic complexes of quercetin exhibit lower as well as higher field shifts that show change in geometry during the metal ligand coordination.\ud
机译:在非水溶液中合成了九种配位的[Ln(槲皮素)(3)] nH(2)O配合物(其中,对于Pr,Sm,Gd,Tb,Dy和Ho,n = 0;对于La和n,n = 3。 Nd)。通过元素分析,摩尔电导,UV-可见光谱,IR光谱,热分析和NMR光谱对络合物进行表征。通过分子建模获得了配合物的优化结构。络合物在DMSO中表现为非电解质。 TGA研究表明配合物的无水性质(La和Nd除外)。在DMSO-d(6)中研究了镧,ase,钕和sa配合物的H-1 NMR光谱。配合物在DMSO中不会解离,并保留其配位数。槲皮素的顺磁性和反磁性配合物的NMR光谱显示出较低和较高的场移,表明在金属配体配位过程中几何形状发生了变化。

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    Ansari, Anees A.;

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  • 年度 2008
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