{"title":"Synthesis and crystal structure of a new isomer of poly[di-μ3-cyanido-μ-2,6-dimethylpyrazine-dicopper(I)]","authors":"Christian Näther","doi":"10.1107/S2056989025006267","DOIUrl":null,"url":null,"abstract":"<div><div>In the crystal structure of the title compound, the copper(I) cations are linked by the cyanide anions into layers that are additionally connected by the 2,6-dimethylpyrazine ligands into a 3D network. The title compound represents a new isomer of Cu<sub>2</sub>(CN)<sub>2</sub>(2,6-dimethylpyrazine), which has already been reported in the literature.</div></div><div><div>The title compound, [Cu<sub>2</sub>(CN)<sub>2</sub>(C<sub>6</sub>H<sub>8</sub>N<sub>2</sub>)]<sub><em>n</em></sub> or Cu<sub>2</sub>(CN)<sub>2</sub>(2,6-dimethylpyrazine), was prepared by the reaction of copper(I) cyanide with 2,6-dimethylpyrazine in water. Its asymmetric unit consists of two crystallographically independent copper(I) cations and cyanide anions as well as one crystallographically independent 2,6-dimethylpyrazine ligand in general positions. Each copper cation is fourfold coordinated by one N atom of the 2,6-dimethylpyrazine ligand and three cyanide anions, that are disordered so that each C and N position has mixed occupancy with a ratio between N and C of 94:6 and 77:23. The copper cations are linked by the cyanide atoms into layers that are further connected into a 3D network by the 2,6-dimethylpyrazine ligands. Powder X-ray diffraction (PXRD) proves that a pure crystalline phase has been obtained. It is noted that this crystal structure represents a new isomer of Cu<sub>2</sub>(CN)<sub>2</sub>(2,6-dimethylpyrazine), which has already been reported in the literature [Chesnut <em>et al.</em> (2001<span><span>#</span></span>). <em>J. Chem. Soc. Dalton Trans</em>. pp. 2567–2580].</div></div>","PeriodicalId":7367,"journal":{"name":"Acta Crystallographica Section E: Crystallographic Communications","volume":"81 8","pages":"Pages 714-717"},"PeriodicalIF":0.6000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Crystallographica Section E: Crystallographic Communications","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2056989025001410","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CRYSTALLOGRAPHY","Score":null,"Total":0}
引用次数: 0
Abstract
In the crystal structure of the title compound, the copper(I) cations are linked by the cyanide anions into layers that are additionally connected by the 2,6-dimethylpyrazine ligands into a 3D network. The title compound represents a new isomer of Cu2(CN)2(2,6-dimethylpyrazine), which has already been reported in the literature.
The title compound, [Cu2(CN)2(C6H8N2)]n or Cu2(CN)2(2,6-dimethylpyrazine), was prepared by the reaction of copper(I) cyanide with 2,6-dimethylpyrazine in water. Its asymmetric unit consists of two crystallographically independent copper(I) cations and cyanide anions as well as one crystallographically independent 2,6-dimethylpyrazine ligand in general positions. Each copper cation is fourfold coordinated by one N atom of the 2,6-dimethylpyrazine ligand and three cyanide anions, that are disordered so that each C and N position has mixed occupancy with a ratio between N and C of 94:6 and 77:23. The copper cations are linked by the cyanide atoms into layers that are further connected into a 3D network by the 2,6-dimethylpyrazine ligands. Powder X-ray diffraction (PXRD) proves that a pure crystalline phase has been obtained. It is noted that this crystal structure represents a new isomer of Cu2(CN)2(2,6-dimethylpyrazine), which has already been reported in the literature [Chesnut et al. (2001#). J. Chem. Soc. Dalton Trans. pp. 2567–2580].
期刊介绍:
Acta Crystallographica Section E: Crystallographic Communications is the IUCr''s open-access structural communications journal. It provides a fast, simple and easily accessible publication mechanism for crystal structure determinations of inorganic, metal-organic and organic compounds. The electronic submission, validation, refereeing and publication facilities of the journal ensure rapid and high-quality publication of fully validated structures. The primary article category is Research Communications; these are peer-reviewed articles describing one or more structure determinations with appropriate discussion of the science.