The 2,2'-bipyridyl-6,6'-dicarboxylate ligand () has been shown in prior work to effectively capture the uranyl(VI) ion, UO, from aqueous solutions. However, the redox properties of the uranyl complex of this ligand have not been addressed despite the relevance of uranium-centered reduction to the nuclear fuel cycle and the presence of a bipyridyl core in , a motif long recognized for its ability to support redox chemistry. Here, the complex of UO () has been synthetically prepared and isolated under nonaqueous conditions for the study of its reductive chemical and electrochemical behavior.
View Article and Find Full Text PDFNew methods for C-N bond construction exploiting the N-centered electrophilic character of iminoquinones are reported. Iminoquinones, generated via the condensation of -vinylanilines with benzoquinones, undergo acid-catalyzed cyclization to afford -arylindoles in excellent yields. Under similar reaction conditions, homoallylic amines react analogously to afford -arylpyrroles.
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