双核钯(II)配合物的合成、表征及生物活性

IF 2.5 Q2 CHEMISTRY, MULTIDISCIPLINARY
Debakanta Tripathy , Soumya Lipsa Rath , Niladri Bihari Debata , Dillip Kumar Chand
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引用次数: 0

摘要

以两种酰胺功能化配体L1和L2分别合成了N,N,N ',N ' -四亚甲基乙二胺(tmeda)保护的钯(II)配合物1和2。配合物1和2经1H、13C NMR、HH COSY、CH COSY和ESI-MS表征。用类似配合物1′和2′的单晶x射线衍射证实了这两种配合物的分子结构。采用赫希菲尔德表面分析方法对晶格中的分子填充进行了评价。结果表明,H…H相互作用是导致配合物1′中分子堆积的主要原因。然而,在配合物2′中,O…H/H…O短接触是晶格的主要稳定因素。利用分子对接工具评价配合物1′和2′的生物活性。这两种复合物均与MexB蛋白相互作用,从结合能值可以看出复合物2′具有较高的结合亲和力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synthesis, characterization and biological activity of binuclear palladium(II) complexes

Synthesis, characterization and biological activity of binuclear palladium(II) complexes
Two N,N,N′,N′-tetramethylethylenediamine (tmeda) protected palladium(II) complexes 1 and 2 were synthesized using two amide functionalized ligands L1 and L2 respectively. Complexes 1 and 2 were characterized by 1H, 13C NMR, HH COSY, CH COSY and ESI-MS. Molecular structures of both the complexes were confirmed by single crystal X-ray diffraction of analogous complexes 1′ and 2′. Molecular packing in the crystal lattice was evaluated using Hirshfeld surface analysis. It was found that the H…H interaction is the major contributor to the molecular packing in complex 1′. However, in complex 2′, O…H/H…O short contact is the major stabilising factor of the crystal lattice. The biological activity of complexes 1′ and 2′ were evaluated using molecular docking tool. Both the complexes were found to interact with MexB protein and complex 2′ having higher binding affinity as evident from the binding energy values.
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来源期刊
Results in Chemistry
Results in Chemistry Chemistry-Chemistry (all)
CiteScore
2.70
自引率
8.70%
发文量
380
审稿时长
56 days
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