首页> 外文期刊>Acta Crystallographica Section E: Crystallographic Communications >Investigation of solid-state photochemical nitro–nitrito linkage isomerization: crystal structures of trans-bis­(ethyl­enedi­amine)(iso­thio­cyanato)­nitritocobalt(III) salts: thio­cyanate, chloride monohydrate, and perchlorate–thio­cyanate­(0.75/0.25)
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Investigation of solid-state photochemical nitro–nitrito linkage isomerization: crystal structures of trans-bis­(ethyl­enedi­amine)(iso­thio­cyanato)­nitritocobalt(III) salts: thio­cyanate, chloride monohydrate, and perchlorate–thio­cyanate­(0.75/0.25)

机译:固态光化学硝基-腈键异构化的研究:反式双(乙二胺)(异硫氰酸根)尼古巴酸(III)盐的晶体结构:硫氰酸盐,一水氯化物和高氯酸盐-硫氰酸盐(0.75 / 0.25)

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The reaction cavities of the nitro groups in the crystals of the title compounds, trans-[Co(NO2)(NCS)(C2H8N2)2]·X, X = SCN− (I), Cl−·H2O (II), and (ClO4−)0.75(SCN−)0.25 (III), have been investigated, revealing that the geometry of the inter­molecular N—H⋯O hydrogen bonds in (I) is unsuitable for nitro–nitrito photo-isomerization. The common main building block of these crystal structures is a centrosymmetric pair of complex cations connected by pairwise N—H⋯O(nitro) hydrogen bonds forming an R22(4) ring, which is a narrow diamond shape in (I) but is approximately square in (II) and (III). The structure of (I) was reported earlier [Börtin (1976). Acta Chem. Scand. A, 30, 503–506] but is described here with an improved disorder model for the thio­cyanate anions and to higher precision.
机译:标题化合物的反式-[Co(NO2)(NCS)(C2H8N2)2]·X,X = SCN-(I),Cl-·H2O(II)和已经研究了(ClO4-)0.75(SCN-)0.25(III),发现(I)中分子间N-H⋯O氢键的几何结构不适合硝化-硝基光异构化。这些晶体结构的共同主要组成部分是通过成对的N-H⋯O(硝基)氢键连接形成R22(4)环的络合阳离子的中心对称对,该环在(I)中为窄菱形,但大约为(II)和(III)中的正方形。 (I)的结构已在早期报道[Börtin(1976)。化学学报。已扫描。 [A,30,503–506],但此处以硫氰酸根阴离子的改进无序模型进行了描述,并且精度更高。

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