A quantum mechanical study on the propagation kinetics of N-methylacrylamide: Comparison with N,N-dimethylacrylamide in free radical polymerization

Abstract

In this study propagation kinetics of free radical polymerization of N-methylacrylamide (NMAAm) is studied with density functional theory calculations. The propagation rate constant ratio of N,N-dimethylacrylamide (DMAAm) and NMAAm (k<inf>NMAAm</inf>/k<inf>DMAAm</inf>) is evaluated via model reactions at dimeric stage. The most favorable modes of addition is shown to be determined by the steric effects and hydrogen bonding interactions between the reactive fragments. Gauche and trans orientations are preferred as the least energetic additions in pro-meso and pro-racemo attacks, respectively. Benchmark studies with various density functionals (M05-2X, M06-2X, MPWB1K, BMK) combined with 6-311+G(3df,2p) basis set assess the calculations. The k<inf>NMAAm</inf>/k<inf>DMAAm</inf> ratio obtained in this study is in line with the experimental value. The addition reaction barrier via dimeric associates in case of NMAAm does not yield significant difference than the barrier via monomeric species. Propagation kinetics in free radical polymerization of N,N-dimethylacrylamide and N-methylacrylamide is modeled with quantum chemical calculations at dimeric model stage. The propagation rate constant ratio of these monomers is calculated with various density functionals. Calculations shed light on the electronic and steric effects and hydrogen bonding interactions within the reactive species that co-play a role in determining the favorable modes of additions. © 2021 Elsevier B.V., All rights reserved.