Visible light-induced radical polymerization of vinyl acetate mediated by organo-nickel N2O2 Schiff-base complexes

Journal of Photochemistry and Photobiology A: Chemistry

Visible light-induced radical polymerization of vinyl acetate mediated by organo-nickel N2O2 Schiff-base complexes

Abstract: Four nickel(II) complexes with symmetrically substituted N2O2 tetradentate Schiff-base ligands, prepared from the 2:1 condensation of 3-tert-butyl-salicylaldehyde, and ethylenediamine (1), o-phenylenediamine (2), 1,2-cis,trans-cyclohexyldiamine (3), or 1,3-diaminepropane (4), were synthesized. These NiII Schiff-base complexes (1–4) were used as control agents for the polymerization of vinyl acetate (VAc) photoinitiated by diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide (TPO) according to a photoinduced organometallic-mediated radical polymerization (photo-OMRP) mechanism. All complexes presented good control ability, although the polymerization mediated by 3 showed the best control over molecular weight (Mn matching Mn,th) and dispersity (Ð < 1.50). The livingness of the polymers has been confirmed by LED on and LED off experiments, the polymerization stopped immediately, and no monomer conversion was observed during the light-off period, indicating a negligible concentration of the active radical in the dark. Further, to demonstrate the living nature of this system, block copolymers of poly(vinyl acetate)-b-poly(methyl acrylate) were synthesized using the sequential visible-light-induced process. Kinetic results and computational investigations supported the activation/deactivation equilibrium exerted by complexes 1–4, which occurred on only one face of the complexes via reversible deactivation (RD) mechanism.

Author(s): Pesqueira, N. M.; Bignardi, C.; Oliveira, L. F.; Machado, A. E. H.; Carvalho-Jr, V. P.; Goi, B. E.

Journal of Photochemistry and Photobiology A: Chemistry

Published: 1 March 2023, Volume 437, 114443

DOI: https://doi.org/10.1016/j.jphotochem.2022.114443

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