کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1310787 1499198 2012 13 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Anion sensing by rhenium(I) carbonyls with polarized N–H recognition motifs
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی معدنی
پیش نمایش صفحه اول مقاله
Anion sensing by rhenium(I) carbonyls with polarized N–H recognition motifs
چکیده انگلیسی

This article describes our recent research results on several rhenium(I) carbonyls complexes with polarized N–H recognition motifs as anion receptors. Structurally simple and easily synthesized luminescent anion receptors containing an amide-type anion binding site and a rhenium(I) tricarbonyl pyridine signaling unit have been developed, and they display outstanding sensitivity and selectivity toward a variety of anionic species. Moreover, thioamides and thiourea derivatives of 2,6-pyridinedicarbonyl dichloride, isophthaloyl dichloride and terephthaloyl dichloride have been synthesized. These ligands have been incorporated in dinuclear rhenium(I) diimine tricarbonyl complexes and provide anion recognition properties in these complexes. Furthermore, the related rhenium(I) complex featuring sulfonamide interacting sites that incorporate the highly chromophoric π-conjugated quinoxaline moiety has been prepared, characterized, and its photophysical properties were also studied.

Anion recognition and sensing has been explored by luminescent rhenium(I) carbonyls containing ligands imparted with polarized N–H groups to serve as the anion recognition motifs. The interactions between rhenium(I) carbonyls and different anions resulted in various degrees of colorimetric and/or luminescent responses that has been attributed to either hydrogen-bonding interactions or proton transfer in some extreme cases.Figure optionsDownload as PowerPoint slideHighlights
► Several rhenium(I) carbonyls complexes with polarized N–H recognition motifs have been synthesized.
► Anion recognition properties of the complexes have been studied by UV–Vis and luminescence spectroscopy.
► Hydrogen-bonding interactions and proton transfer processes have been investigated.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Inorganica Chimica Acta - Volume 389, 1 July 2012, Pages 16–28
نویسندگان
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