On-surface synthesis involving the homocoupling of aryl-alkynes affords the buildup of bisacetylene derivatives directly at surfaces, which in turn may be further used as ingredients for the production of novel functional materials. Generally, homocoupling of terminal alkynes takes place by thermal activation of molecular precursors on metal surfaces. However, the interaction of alkynes with surface metal atoms often induces unwanted reaction pathways when thermal energy is provided to the system. In this contribution we report about light-induced metal-free homocoupling of terminal alkynes on highly oriented pyrolitic graphite (HOPG). The reaction occurred with high efficiency and selectivity within a self-assembled monolayer (SAM) of aryl-alkynes and led to the generation of large domains of ordered butadiynyl derivatives. Such a photochemical uncatalyzed pathway represents an original approach in the field of topological C-C coupling at the solid/liquid interface.
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http://dx.doi.org/10.1021/jacs.6b03589 | DOI Listing |
Angew Chem Int Ed Engl
January 2025
Center of Basic Molecular Science (CBMS), Department of Chemistry, Tsinghua University, Beijing, 100084, China.
Perchlorate, initially regarded as a weakly coordinating counterion rather than a reactive oxidizing reagent due to its kinetic stability, has garnered attention for its potential in microbial systems. Under anaerobic conditions, microbes utilize perchlorate as a terminal oxidant for methane oxidation, involving two distinct stages: extraction and release of oxidizing ability. This two-phase activation process necessitates the collaborative action of multiple enzymes, a phenomenon not extensively explored in artificial systems.
View Article and Find Full Text PDFDalton Trans
November 2024
Institute for Inorganic Chemistry, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074 Würzburg, Germany.
The carbene-stabilised beryllium Grignards [(CAAC)BeBrR] (R = CAACH 1a, Dur 1b; CAAC/H = 1-(2,6-dipropylphenyl)-2,2,4,4-tetramethylpyrrolidin-2-yl/idene; Dur = 2,3,5,6-tetramethylphenyl) undergo salt metathesis with various pseudohalide salt precursors. Whereas with [NaNCS] the thiocyanato Grignards [(CAAC)Be(NCS)R] (R = CAACH 2a, Dur 2b) are obtained selectively, salt metatheses with [Na(OCP)(dioxane)] and [K(OCN)] are fraught with side reactions, in particular scrambling of both neutral and anionic ligands, leading to complex product mixtures, from which the first examples of beryllium phosphaethynolate Grignards [(thf)(CAACH)Be(OCP)] (3) and [(CAAC)Be(OCP)R] (R = CAACH 4a, Dur 4b), as well as the isocyanate-bridged hexamer [(CAAC)BrBe(1,3-μ-OCN)] (7) were determined as the main products. The complexity of possible side reactions is seen in complex 5, a byproduct of the salt metathesis of 1b with [Na(OCP)(dioxane)], which hints at radical redox processes, OCP homocoupling, OCP coupling with CAAC, as well as OCP insertion into the Be-R bond.
View Article and Find Full Text PDFJ Am Chem Soc
October 2024
Department of Physics, City University of Hong Kong, Kowloon 999077, Hong Kong SAR, China.
Formation of new chemical species has been achieved under an electric field by the use of the scanning tunneling microscope break junction technique, yet simultaneous implementation of catalytic reactions both at the organic/metal interface and in the bulk solution remains a challenging task. Herein, we show that -butyl-substituted organotin-terminated benzene undergoes both an efficient cleavage of the terminal tributyltin group to form a covalent Au-C bond and a homocoupling reaction to yield biphenyl product when subjected to an electric field in the vicinity to Au electrodes. By using ex situ characterization of high-performance liquid chromatography with an UV-vis detector, we demonstrate that the homocoupling reaction can occur with high efficiency under an extremely low tip bias voltage of ∼5 mV.
View Article and Find Full Text PDFNano Lett
August 2024
Department of Chemistry, University of Southern California, Los Angeles, California 90089, United States.
Nonpolar solvents commonly used in scanning tunneling microscope-based break junction measurements exhibit hazards and relatively low boiling points (bp) that limit the scope of solution experiments at elevated temperatures. Here we show that low toxicity, ultrahigh bp solvents such as bis(2-ethylhexyl) adipate (bp = 417 °C) and squalane (457 °C) can be used to probe molecular junctions at ≥100 °C. With these, we extend solvent- and temperature-dependent conductance trends for junction components such as 4,4'-bipyridine and thiomethyl-terminated oligophenylenes and reveal the gold snapback distance is larger at 100 °C due to increased surface atom mobility.
View Article and Find Full Text PDFACS Nano
May 2024
Center for Basic Research on Materials, National Institute for Materials Science, 1-2-1 Sengen, Tsukuba, Ibaraki 305-0047, Japan.
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