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具有较重硫属元素次膦酸酯供体位点的对称P-立体中心二茂铁配体。

-Symmetric P-Stereogenic Ferrocene Ligands with Heavier Chalcogenophosphinous Acid Ester Donor Sites.

作者信息

Franz Roman, Bruhn Clemens, Pietschnig Rudolf

机构信息

Institute for Chemistry and CINSaT, University of Kassel, Heinrich Plett-Straße 40, 34132 Kassel, Germany.

出版信息

Molecules. 2021 Mar 27;26(7):1899. doi: 10.3390/molecules26071899.

Abstract

-Butyl-substituted diphospha[2]ferrocenophane was used as a stereochemically confined diphosphane to investigate the addition of various dichalcoganes (R2Ch2; Ch = S, Se, Te and R = Me, Ph). Bischalcogenophosphinous acid esters bearing four soft donor sides were obtained as a mixture of and diastereomers and characterized by means of multinuclear NMR and X-ray analysis. The coordination chemistry of multidentate ligand was explored toward d coinage metal centers (Cu(I), Ag(I), and Au(I)), yielding various bimetallic complexes.

摘要

-丁基取代的二磷杂[2]二茂铁烯被用作立体化学受限的二膦,以研究各种二硫属元素化合物(R2Ch2;Ch = S、Se、Te且R = Me、Ph)的加成反应。得到了具有四个软供体侧的双硫属元素次膦酸酯,它是一对非对映异构体的混合物,并通过多核核磁共振和X射线分析对其进行了表征。研究了多齿配体与d族货币金属中心(Cu(I)、Ag(I)和Au(I))的配位化学,得到了各种双金属配合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8a9/8037359/102689f7c311/molecules-26-01899-sch001.jpg

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