RESUMO
The synthesis of TBA-DASA-POM-DASA, the first photoactive covalent hybrid polyoxometalate (POM) incorporating a donor-acceptor Stenhouse adduct (DASA) reverse photochrome, is presented. It has been evidenced that in solution the equilibrium between the colorless cyclopentenone and the highly colored triene conformers is strongly dependent not only on the nature of the solvent but also the countercations, allowing to tune its optical properties. This complex has been further associated to photochromic spironaphtoxazine cations, resulting in a material which can be activated by two distinct optical stimuli. Moreover, when combined with N-methyldiethanolamine, TBA-DASA-POM-DASA constitutes a performing photoinitiating system for polyethylene glycol diacrylate polymerization and under visible light irradiation, a promising result in a domain scarcely developed in POM chemistry.
RESUMO
Photoinitiating systems combining 2,6-diaminoanthraquinone (AQD), iodonium salt (Iod), and benzyl alcohol derivatives have been developed to efficiently initiate the cationic polymerization of epoxy monomers upon light exposure. Electron spin resonance spin-trapping (ESR ST) experiments, fluorescence investigations, and steady-state photolysis have demonstrated that a dye-sensitized reaction occurs between AQD and the benzyl alcohol derivatives through a hydrogen abstraction mechanism upon light illumination, followed by reduction of Iod. The inâ situ liberation of protic acids promotes the cationic photopolymerization of epoxy monomers concomitantly with hydrolysis and condensation of the reactive methoxysilanes of an organic-inorganic precursor, for example, 3-glycidyloxypropyltrimethoxysilane (GPTMS). Nanoindentation experiments and scratch resistance tests proved that the resulting GPTMS coatings exhibit very good resistance to brittle fracture and excellent adherence to stainless-steel substrates. Interestingly, antibacterial tests of the GPTMS coatings showed efficient antifouling and biocide properties against E.â coli and S.â aureus.