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Charge-Transfer Complexes as New Inhibitors/Photoinitiatorsfor On-Demand Amine/Peroxide Redox Polymerization

机译:电荷转移复合物作为新的抑制剂/光引发剂用于按需胺/过氧化物氧化还原聚合

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摘要

Redox free-radical polymerizations have widespread applications but still clearly suffer from poor time control of the reaction. Currently, the workability (delay of the gel time) in redox polymerization after mixing is possible thanks to two main types of inhibitors (radical scavengers): phenols and nitroxides. Out of this trend, we propose in this work an alternative strategy for time delaying of the redox polymerization, which is based on charge-transfer complexes (CTCs). Thanks to iodonium salt complexation, the amine (here 4-N,N-trimethylaniline) is proposed to be stored in a CTC equilibrium and is slowly released over a period of time (as a result of the consumption of free amines by peroxides). This alternative strategy allowed us to double the gel time (e.g., from 60 to 120 s) while maintaining a high polymerization efficiency (performance comparable to reference nitroxides). More interestingly, the CTCs involved in this retarding strategy are photoresponsive under visible LED@405 nm and can be used on demand as photoinitiators, allowing (i) spectacular increases in polymerization efficiencies (from 50 °C withoutlight to 120 °C under mild irradiation conditions); (ii) drasticreduction of the oxygen-inhibited layer (already 45% C=C conversionat a 2 μm distance from the top surface) compared to the nonirradiatedsample (thick inhibited layer of more than 45 μm); and (iii)external control of the redox polymerization gel time due to the possiblelight activation.
机译:氧化还原自由基聚合具有广泛的应用,但是显然仍然受反应时间控制不良的困扰。目前,由于两种主要类型的抑制剂(自由基清除剂):酚和氮氧化物,混合后氧化还原聚合的可加工性(凝胶时间的延迟)成为可能。出于这种趋势,我们在这项工作中提出了一种基于电荷转移配合物(CTC)的氧化还原聚合反应时间延迟的替代策略。由于碘鎓盐的络合,建议将胺(此处为4-N,N-三甲基苯胺)存储在四氯化碳平衡中,并在一段时间内缓慢释放(由于过氧化物消耗了游离胺)。这种替代策略使我们可以将胶凝时间加倍(例如从60秒增加到120秒),同时保持较高的聚合效率(性能可媲美参比氮氧化物)。更有趣的是,参与这种阻滞策略的四氯化碳在可见光下在405nm的LED下具有光响应性,可以按需用作光引发剂,从而使(i)聚合效率显着提高(从50°C开始,而没有在温和的照射条件下光照至120°C); (ii)激烈减少氧气抑制层(已经达到45%的C = C转化率)距顶面2μm的距离)样品(厚抑制层大于45μm);和(iii)由于可能,对氧化还原聚合凝胶时间的外部控制光激活。

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