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一种异碲唑氮氧化物的不寻常大环六聚体通过与Fe(II)和Ni(II)的κ -O配位形成,其具有CTe O硫族元素键。

An Unusual Macrocyclic Hexamer of an Iso-Tellurazole N-Oxide Featuring CTe O Chalcogen Bonds is Formed by κ -O Complexation to Fe(II) and Ni(II).

作者信息

Wang Jin, Ho Peter C, Craig Matthew G J, Cevallos Alberto, Britten James F, Vargas-Baca Ignacio

机构信息

Department of Chemistry and Chemical Biology, McMaster University, 1280 Main Street West, Hamilton, Ontario, L8S 4M1, Canada.

出版信息

Chemistry. 2024 Jan 11;30(3):e202302538. doi: 10.1002/chem.202302538. Epub 2023 Nov 20.

Abstract

Studies of the supramolecular chemistry of iso-tellurazole N-oxides have been confined to non-polar media until now. To overcome that limitation, an iso-tellurazole N-oxide was derivatized with a primary alcohol group; the compound is soluble in polar solvents and stable in acidic to neutral aqueous media. Nickel (II) and iron (II) form macrocyclic complexes with six molecules of that iso-tellurazole N-oxide in a hitherto not-observed macrocyclic arrangement defined by CTe⋅⋅⋅O chalcogen bonds and κ -O bound to the metal ion. This behaviour is in sharp contrast with the κ -Te (n=1,2,4) complexes formed by soft metal ions.

摘要

迄今为止,异碲唑N - 氧化物的超分子化学研究一直局限于非极性介质。为了克服这一限制,一种异碲唑N - 氧化物被衍生出一个伯醇基团;该化合物可溶于极性溶剂,且在酸性至中性水性介质中稳定。镍(II)和铁(II)与六个该异碲唑N - 氧化物分子形成大环配合物,其大环排列由CTe⋅⋅⋅O硫族键和与金属离子结合的κ - O定义,这是一种迄今未被观察到的排列方式。这种行为与软金属离子形成的κ - Te(n = 1,2,4)配合物形成了鲜明对比。

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