Université de Haute-Alsace, CNRS, IS2M UMR 7361, F-68100 Mulhouse, France.
Université de Strasbourg, Strasbourg F-67081, France.
Molecules. 2020 Mar 31;25(7):1602. doi: 10.3390/molecules25071602.
Currently, Redox Initiating Systems (RISs) of Free Radical Polymerization (FRP) are mainly based on the interaction of aromatic amines with peroxides (e.g., dibenzoyl peroxide (BPO)) that can be both toxic and unstable. In the present work, we aim to replace these hazardous substances in new RIS that can be peroxide-free and amine-free. Our redox two components (2K) initiating system is based on diphenylsilane (DPS) as reducing agent combined with different metal complexes (Mn(acac), Cu(AAEMA) or Fe(acac)) as oxidizing agents. For the new proposed RIS, an excellent reactivity is found for the polymerization of benchmark methacrylate monomers under mild conditions (redox polymerization done under air and at room temperature); remarkably, it is also possible to finely control the gel time. Different techniques (optical pyrometry, Real-Time FTIR spectroscopy, Cyclic Voltammetry and Electron Spin Resonance (ESR)) were used to follow the polymerization processes but also to shed some light on the new redox chemical mechanisms.
目前,自由基聚合(FRP)的氧化还原引发体系(RIS)主要基于芳香胺与过氧化物(如过氧化二苯甲酰(BPO))的相互作用,而过氧化物既有毒又不稳定。在本工作中,我们旨在用无过氧化物和无胺的新 RIS 取代这些危险物质。我们的氧化还原双组分(2K)引发体系基于二苯基硅烷(DPS)作为还原剂,与不同的金属配合物(Mn(acac)、Cu(AAEMA)或 Fe(acac))作为氧化剂。对于新提出的 RIS,在温和条件下(氧化还原聚合在空气和室温下进行),发现对基准甲基丙烯酸酯单体的聚合具有优异的反应性;值得注意的是,还可以精细控制凝胶时间。使用不同的技术(光学高温计、实时傅里叶变换红外光谱、循环伏安法和电子自旋共振(ESR))来跟踪聚合过程,但也可以揭示新的氧化还原化学机制。