Organobismuthines are an attractive class of organometallic reagents that can be accessed from inexpensive and nontoxic bismuth salts. Triarylbismuthines are particularly interesting due to their air and moisture stability and high functional group tolerance. We report herein a detailed study on the preparation of highly functionalized triarylbismuth reagents by triple functional group manipulation and their use in palladium- and copper-catalyzed C-, N-, and O-arylation reactions.

The synthesis of a new hydrophilic ammonium-based poly(ethylene glycol)-ionic liquid (PEG-IL) is reported; the structure was assigned by NMR ((1)H, (13)C) and MALDI mass spectrometry. The viscosity and thermal stability were also studied, as well as its polarity. Its application as an alternative solvent in the synthesis of dipeptides under microwave irradiation is also described.

This report describes the synthesis, characterization, and reactivities of the pincer-type complexes κ). These complexes were prepared by treating their Ni−Br analogues with excess AgF at rt (2a and 2b) or excess AgF and Me 3 SiCF 3 (3a and 3b) at 45 °C. The Ni−F derivative 2a was shown to be an intermediate for the formation of the Ni−CF 3 derivative 3a. Complexes 2a, 3a, and 3b were fully characterized by multinuclear NMR spectroscopy, cyclic voltammetry, and X-ray diffraction analysis. Variable temperature, multinuclear NMR analysis of 2a helped elucidate interaction of the fluoride ligand with hydrofluoric acid present in the reaction medium. The bromo complexes 1a or 1b catalyzed fluorination of benzyl halides at 90 °C in the presence of excess AgF, whereas the Ni−CF 3 complexes 3 failed to promote trifluoromethylation of benzyl bromide, leading instead to a direct benzylation of the aromatic reaction solvent (benzene, toluene, xylene, or bromobenzene). Possible mechanisms for this benzylation reaction have been probed and discussed.

Highly functionalized diaryl ethers were prepared by copper(II) acetate mediated O-arylation reaction of phenols using trivalent organobismuthanes. The reaction is performed under simple conditions and tolerates a wide diversity of functional groups on the phenol and on the organobismuth reagent. Substoichiometric amounts of catalyst can be used by performing the reaction under an oxygen atmosphere. The N-arylation of pyridones is also reported.

The N-arylation of indoles, indazoles, pyrroles, and pyrazoles using highly functionalized trivalent arylbismuth reagents is reported.