28 اردیبهشت 1403
قدرت محمودي

قدرت محمودی

مرتبه علمی: دانشیار
نشانی: آذربایجان شرقی، مراغه، میدان مادر، بلوار دانشگاه، دانشگاه مراغه - دانشکده علوم پایه - گروه شیمی معدنی
تحصیلات: دکترای تخصصی / شیمی معدنی
تلفن:
دانشکده: دانشکده علوم پایه

مشخصات پژوهش

عنوان
Non-covalent interactions induced supramolecular architecture of Hg(NCS)2 with 3-pyridinecarbaldehyde nicotinoylhydrazone
نوع پژوهش مقاله چاپ شده
کلیدواژه‌ها
Coordination chemistryMercuryNoncovalent interactionX-ray crystallographyDFT
سال
2020
مجله INORGANICA CHIMICA ACTA
شناسه DOI 10.1016/j.ica.2020.119700
پژوهشگران جوان ولاسکوئز ، قدرت محمودی ، اننیو زانگراندو ، باربارا میراسلو ، دمیر سفین ، جورج اچیویریا

چکیده

In this work we have synthesized and characterized a new HgII complex [Hg(HL)(NCS)2]2, fabricated from Hg(NCS)2 and 3-pyridinecarbaldehyde nicotinoylhydrazone (HL). Single-crystal X-ray crystallography reveals the formation of a dinuclear heteroleptic discrete structure with half of the molecule, [Hg(HL)(SCN)2], in the asymmetric unit. The ligand HL coordinates the HgII center in an unexpected monodentate fashion via the pyridine nitrogen of the nicotinic moiety. Molecules are aggregated through intermolecular N–H∙∙∙N hydrogen bonds and additional weak Hg∙∙∙N interactions. Molecules of complex aggregate into a 2D supramolecular layer with a four-connected uninodal sql (Shubnikov tetragonal plane net) topology due to intermolecular N–H∙∙∙N hydrogen bonds. When the Hg∙∙∙N interactions are excusively considered, a similar layer is formed revealing a three-connected uninodal hcb (Shubnikov hexagonal plane net) topology. Further considering both the intermolecular N–H∙∙∙N hydrogen bonds and Hg∙∙∙N interactions, the structure of complex can be extended into a 3D supramolecular framework with an eight-connected uninodal bcu (body centered cubic) topology. We have also applied DFT calculations as well as MEP, QTAIM, NCI and NBO analyses to shed light on interactions in the crystal structure of the complex. Among others, reciprocal n → π* interactions between the nitrogen lone pairs and empty antibonding π* C–N orbitals of the NCS– anions have been determined.