Silver acetylides are among the oldest organometallics known; however, their applications in organic chemistry remained scarce until very recently. Indeed, several reactions involving silver salts as catalyst or silver acetylides have been reported in the past five years. The extreme mildness and very low basicity of these nucleophilic reagents nicely complement the behavior of other alkynyl metals, rendering them very useful in various transformations, especially in the synthesis of complex molecules. Silver acetylides are now seen as promising tools in organic chemistry. This critical review focuses on this emerging field, and, with emphasis on mechanistic aspects, cover the synthesis of silver acetylides, their applications in organic chemistry and reactions involving silver salts as catalysts where silver acetylides are probable intermediates.
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http://dx.doi.org/10.1039/b602151b | DOI Listing |
Chem Commun (Camb)
September 2024
Universite de Pau et Pays de l'Adour, E2S UPPA, CNRS, IPREM UMR 5254 Technopole Hélioparc 2 avenue du Président Pierre Angot, 64053 PAU CEDEX 09, France.
A one-step synthesis of porphyrin-silver acetylide clusters from tetra alkyne-substituted porphyrin is described. The solid-state properties of three 2D-like compounds were fully characterised using XPS and XRD while their catalytic properties under CO electroreduction reaction conditions were assessed and their faradaic efficiency quantified.
View Article and Find Full Text PDFJ Am Chem Soc
August 2023
Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa K1N 6N5, Canada.
The introduction of the copper-catalyzed azide-alkyne coupling (CuAAC) to 1,3-dipolar cycloadditions was pivotal to their popularization in synthetic chemistry and to their application to multiple other domains of science. The reaction rate enhancement observed when coinage metal acetylide intermediates are involved in the cyclization process greatly expanded the structural and conditional range in which (3 + 2) cycloadditions may take place with terminal alkynes. Herein, we report that comparable rate enhancements, in nature and level, are induced by copper and silver catalysts in the intramolecular (3 + 2) cycloaddition of terminal alkynes with "neutral" three-atom components (TACs), specifically alkynyl sulfides.
View Article and Find Full Text PDFNanomaterials (Basel)
May 2022
Institute for Applied and Physical Chemistry (IAPC), Fachbereich 2 (Chemie/Biologie), University of Bremen, Leobener Str. 5 (NW2), 28359 Bremen, Germany.
Focused electron beam induced deposition (FEBID) is a versatile tool to produce nanostructures through electron-induced decomposition of metal-containing precursor molecules. However, the metal content of the resulting materials is often low. Using different Ag(I) complexes, this study shows that the precursor performance depends critically on the molecular structure.
View Article and Find Full Text PDFChem Commun (Camb)
December 2020
DST Unit of Nanoscience (DST UNS) and Thematic Unit of Excellence (TUE), Department of Chemistry, Indian Institute of Technology Madras, Chennai 600 036, India.
We present the first example of acetylide protected silver clusters by a reaction between Ag and acetylene, conducted around atmospheric pressure. The products were obtained after dehydrogenation of acetylene in the gas phase. The observed reaction mechanism may be helpful to design new catalysts useful in organometallic chemistry.
View Article and Find Full Text PDFRSC Adv
November 2020
Leibniz-Institut für Festkörper- und Werkstoffforschung Dresden Helmholtzstr. 20 01069 Dresden Germany
A novel ruthenium-acetylide complex was synthesised and characterised in solid state and solution. Thin films of the complex were evaporated on silver and gold foils in ultra high vacuum in order to probe the electronic properties with photoemission spectroscopy. The charge transfer characteristics of the complex with the strong acceptor FTCNNQ were investigated by UV-vis absorption in solution as well as at an interface with photoemission spectroscopy.
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