Computational design of next generation atom transfer radical polymerization ligands

Benchmarked density functional theory is used to design and evaluate a series of novel atom transfer radical polymerization (ATRP) catalysts with a view to identifying those which best promote a model ATRP reaction between the [LCuI](+) catalyst and methyl alpha-bromoisobutyrate in acetonitrile. Calculations were performed at the omega B97XD/Def2TZVP//omega B97XD/SDD/6-31G(d) level of theory with CPCM solvent corrections. Locating the axial N of the tetradentate ATRP ligand at a sterically unhindered quinuclidine bridgehead site, with the cage carrying three pendant 2-pyridyl arms to serve as equatorial ligands causes a significant increase in activity. The effects are greater for the CH2-linked quinuclidine cages compared with the O-linked cages, although both systems out-perform the best available ATRP ligands in current use. Inclusion of this cage structure introduces opportunities for stereoisomerism, and while all stereoisomers examined function as effective catalysts, there is significant variation in performance. Incorporation of electron donating 4-(dialkylamino) groups on the 2-pyridyl arms improves ligand activity by stabilizing Cu-II over Cu-I, however, one needs to be careful of unfavorable steric crowding, particularly for some stereoisomers. Replacing the 2-pyridyl arms with other types of neutral heterocycles, such as NHC-containing heterocycles and imidazoles, does not appear to offer an advantage over pyridine. However, ligands with negatively charged donor nitrogens could offer 10 orders of magnitude improvement in catalyst activity over the best available neutral ligands, which could help make ATRP and other small molecule processes that employ ATRP catalysts applicable to unactivated alkyl halides.

Automated summary

Benchmarked density functional theory is used to design and evaluate a series of novel atom transfer radical polymerization (ATRP) catalysts, among which the cage structure with 2-pyridyl arms performs the best. There are significant differences in catalytic performance among different stereoisomers, and the incorporation of electron donating groups improves ligand activity. Replacing 2-pyridyl arms with other neutral heterocycles does not offer much advantage, while ligands with negatively charged donor nitrogens can greatly enhance catalyst activity.