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苯并咪唑和吡啶基咔唑衍生物的碘(I)和银(I)配合物

Iodine(I) and Silver(I) Complexes of Benzoimidazole and Pyridylcarbazole Derivatives.

作者信息

Taipale Essi, Siepmann Marcel, Truong Khai-Nghi, Rissanen Kari

机构信息

University of Jyvaskyla, Department of Chemistry, P.O. Box 35, Survontie 9B, 40014, Jyväskylä, Finland.

出版信息

Chemistry. 2021 Dec 9;27(69):17412-17419. doi: 10.1002/chem.202103152. Epub 2021 Oct 15.

Abstract

The synthesis of iodine(I) complexes with either benzoimidazole or carbazole-derived sp N-containing Lewis bases is described, as well as their corresponding silver(I) complexes. The addition of elemental iodine to the linear two-coordinate Ag(I) complexes produces iodine(I) complexes with a three-center four-electron (3c-4e) [N-I-N] bond. The H and H- N HMBC NMR studies unambiguously confirm the formation of the complexes in all cases via the [N-Ag-N] →[N-I-N] cation exchange, with the N NMR chemical shift change between 94 to 111 ppm when compared to the free ligand. The single crystal X-ray crystallographic studies on eight I complexes revealed highly symmetrical [N-I-N] bonds with I-N bond distances of 2.21-2.26 Å and N-I-N angles of 177-180°, whilst some of the corresponding Ag complexes showed a clear deviation from linearity with N-Ag-N angles of ca. 150° and Ag-N bond distances of 2.09-2.18 Å.

摘要

本文描述了碘(I)与苯并咪唑或咔唑衍生的含sp氮的路易斯碱形成的配合物,以及它们相应的银(I)配合物。向线性二配位Ag(I)配合物中加入单质碘会生成具有三中心四电子(3c-4e)[N-I-N]键的碘(I)配合物。1H和1H-15N HMBC NMR研究明确证实,在所有情况下,配合物都是通过[N-Ag-N]→[N-I-N]阳离子交换形成的,与游离配体相比,15N NMR化学位移在94至111 ppm之间变化。对八个碘配合物的单晶X射线晶体学研究表明,[N-I-N]键具有高度对称性,I-N键距离为2.21-2.26 Å,N-I-N角度为177-180°,而一些相应的银配合物则明显偏离线性,N-Ag-N角度约为150°,Ag-N键距离为2.09-2.18 Å。

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