O. V. Loseva, T. A. Rodina, A. I. Smolentsev, S. V. Zinchenko, A. V. Ivanov
{"title":"The Tetranuclear Macrocyclic Mercury(II) Complex of [Hg4{S2CN(CH3)2}4Cl4]: Preparation, Molecular and Supramolecular Structures, and Thermal Behavior","authors":"O. V. Loseva, T. A. Rodina, A. I. Smolentsev, S. V. Zinchenko, A. V. Ivanov","doi":"10.1134/S1070328424600906","DOIUrl":null,"url":null,"abstract":"<p>The tetranuclear mercury(II) dithiocarbamatо-chloridо complex [Hg<sub>4</sub>(S<sub>2</sub>CNMe<sub>2</sub>)<sub>4</sub>Cl<sub>4</sub>] (<b>I</b>), whose molecule includes the centrosymmetric 16-membered metallacycle [Hg<sub>4</sub>S<sub>8</sub>C<sub>4</sub>], was prepared by the reaction of solutions of HgCl<sub>2</sub> and sodium dimethyldithiocarbamate (Me<sub>2</sub>Dtc). The crystal, molecular, and supramolecular structures of <b>I</b> were established using direct method of single-crystal X-ray diffraction (CCDC no. 2364847). In complex <b>I</b>, the non-equivalent μ<sub>2</sub>-bridging dithiocarbamate ligands link neighboring mercury atoms in pairs, thus forming a tetranuclear macrocyclic molecule. The intramolecular Hg···S and Hg···Cl secondary bonds stabilize the spatial configuration of this macrometallacycle. The supramolecular self-organization of the complex is due to the relatively weak, pairwise S···Cl and Hg···Cl secondary interactions, which combine the tetranuclear molecules of <b>I</b> into 2D pseudo-polymer layers; numerous non-classical C–H···Cl and C–H···S hydrogen bonds connect these layers to form a 3D framework. According to simultaneous thermal analysis data, the thermal decomposition of <b>I</b> is accompanied by the formation of HgS and release of HgCl<sub>2</sub>.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"51 1","pages":"47 - 57"},"PeriodicalIF":1.1000,"publicationDate":"2025-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Russian Journal of Coordination Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1134/S1070328424600906","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0
Abstract
The tetranuclear mercury(II) dithiocarbamatо-chloridо complex [Hg4(S2CNMe2)4Cl4] (I), whose molecule includes the centrosymmetric 16-membered metallacycle [Hg4S8C4], was prepared by the reaction of solutions of HgCl2 and sodium dimethyldithiocarbamate (Me2Dtc). The crystal, molecular, and supramolecular structures of I were established using direct method of single-crystal X-ray diffraction (CCDC no. 2364847). In complex I, the non-equivalent μ2-bridging dithiocarbamate ligands link neighboring mercury atoms in pairs, thus forming a tetranuclear macrocyclic molecule. The intramolecular Hg···S and Hg···Cl secondary bonds stabilize the spatial configuration of this macrometallacycle. The supramolecular self-organization of the complex is due to the relatively weak, pairwise S···Cl and Hg···Cl secondary interactions, which combine the tetranuclear molecules of I into 2D pseudo-polymer layers; numerous non-classical C–H···Cl and C–H···S hydrogen bonds connect these layers to form a 3D framework. According to simultaneous thermal analysis data, the thermal decomposition of I is accompanied by the formation of HgS and release of HgCl2.
期刊介绍:
Russian Journal of Coordination Chemistry is a journal that publishes reviews, original papers, and short communications on all aspects of theoretical and experimental coordination chemistry. Modern coordination chemistry is an interdisciplinary science that makes a bridge between inorganic, organic, physical, analytical, and biological chemistry.