This research uncovers a novel method for creating palladium NHC complexes using triazolium salts, suggesting implications for synthetic chemistry.
We report the first example of direct C-H oxidative addition of 1,2,4-triazolium salts to Pd2(dba)3, providing a new route to palladium N-heterocyclic carbene (NHC) complexes. Three triazolium ligands, 4-benzyl-1-butyl-1,2,4-triazolium bromide, 4-benzyl-1-methyl-1,2,4-triazolium bromide and 1,4-dibutyl-1,2,4-triazolium bromide were synthesized and reacted with Pd2(dba)3. This reaction occurs in air and proceeds efficiently in 1-3 hours to afford air stable, mostly trans, [Pd(NHC)2Br2] complexes. The complexes are isolated in good yield and fully characterized. All complexes exhibit NMR evidence of rotamers (anti and syn). The structures of three complexes were confirmed by single-crystal X-ray diffraction.
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Kovacevic et al. (2025) studied this question.
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