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Article Abstract

An extended trisazo dipyridyl ligand, , and its copper(I) complex, [], were synthesized and fully characterized. Complex [] has five coordination geometry satisfied by ligand . has a low-lying π* orbital; thus, [] showed very facile multiple ligand-based redox events. Moreover, due to the strong π-acceptor nature of , the Cu(II)/Cu(I) redox potential of [] was anodic (0.62 V). The redox events of both and [] were characterized using various spectroscopic studies and density functional theory (DFT) calculations. Taking advantage of the multiple facile ligand-based reductions in [], the Glaser coupling reaction of terminal alkynes was explored. Various kinds of alkynes were found to be effective when using [] as a precatalyst. The mechanism of the reaction was investigated thoroughly by several controlled experiments, isolation, and characterization of the intermediates using various spectroscopic studies as well as by single-crystal X-ray structure determination. These studies showed that the in [] acted not only in the electron transfer events but also as a locus for binding the substrate, breaking and forming bonds, and, finally, releasing the product. Thus, here, the metal mainly acted as a spectator and ligand acted as an actor.

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http://dx.doi.org/10.1021/acs.inorgchem.4c03210DOI Listing

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