Unlocking Structurally Nontraditional Naphthyridine-Based Electron-Transporting Materials with C-H Activation-Annulation.
Sign Up to like & getrecommendations! Published in 2024 at "Journal of the American Chemical Society"
DOI: 10.1021/jacs.3c14297
Abstract: The inherent benefits of C-H activation have given rise to innovative approaches in designing organic optoelectronic molecules that depart from conventional methods. While theoretical calculations have suggested the suitability of the 2,6-naphthyridine scaffold for electron… read more here.
Keywords: unlocking structurally; activation annulation; structurally nontraditional; activation ... See more keywords
Dicopper(I) complexes of a binucleating, dianionic, naphthyridine bis(amide) ligand.
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DOI: 10.1039/d5dt00034c
Abstract: The dinucleating ligand, 1,8-naphthyridine-2,7-bis(2,6-diisopropylphenyl)carboxamide (NBDA), was synthesized by palladium-catalyzed aminocarbonylation. This ligand was treated with two equivalents of mesitylcopper(I) in the presence of [nBu4N]X (X = Cl, N3) to give the anionic complexes [nBu4N][Cu2(NBDA)(μ-Cl)] and… read more here.
Keywords: cu2 nbda; dicopper complexes; ligand; naphthyridine ... See more keywords