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具有自主后转化功能的(甲基)丙烯酸酯聚合反应的可见光光引发

Visible-Light Photoinitiation of (Meth)acrylate Polymerization with Autonomous Post-conversion.

作者信息

Kim Kangmin, Sinha Jasmine, Stansbury Jeffrey W, Musgrave Charles B

机构信息

Chemistry, University of Colorado, Boulder, Colorado 80309, United States.

Chemical and Biological Engineering, University of Colorado, Boulder, Colorado 80309, United States.

出版信息

Macromolecules. 2021 Sep 14;54(17):7702-7715. doi: 10.1021/acs.macromol.1c00761. Epub 2021 Aug 17.

Abstract

Conversion plateaus rapidly in radical photopolymerizations (RPPs) following discontinuation of irradiation due to rapid termination of reactive radicals, which restricts the wider use of RPPs in applications that involve nonuniform light access including those with attenuated light transmission or irregular surfaces. Based on our recent report of a radical dark-curing photoinitiator (DCPI) that continues polymerization beyond the cessation of irradiation by enabling latent redox initiation with photo-released amine in the presence of a suitable oxidant, we developed a new DCPI with an absorption spectrum that extends well into the visible range. Our design process involved a series of computational investigations of candidate molecules, including a systematic study of substituents and their position-dependent effects on absorption characteristics, electronic transitions, and the photochemical mechanism and its associated energetics. Our quantum chemical computations identified the target compound 5,7-dimethoxy-6-bromo-3-aroylcoumarin-DMPT/BPh and predicted that it would facilitate the dark-curing mechanism by concurrent photo-radical generation and photo-induced release of an efficient redox reductant under visible irradiation. This reductant-tethered chromophore was then synthesized and optically characterized with UV-vis spectroscopy that revealed its strong visible-light absorption with a molar absorptivity of 5710 M cm at 405 nm and 50 M cm at 455 nm. We then demonstrated extensive dark-curing of >35% additional conversion over 25 min following brief activation of the shelf-stable one-part system by irradiation with a 455 nm LED that was ceased at 20% conversion. In contrast, shuttering irradiation of the control formulation at that same point resulted in immediate cessation of conversion, which plateaued at 20%. We determined a remarkable initiator efficiency of 2.82 that results from the additional redox-generated radicals with a 77% photo-reductant generation quantum yield. The combination of superior photo- and dark-curing efficiencies of this new visible DCPI is expected to open new application opportunities in RPP, especially those involving resins that are highly light attenuating, surfaces that possess irregular features that produce uneven irradiance, and production lines where continued dark-curing downstream of the light activation step enhances line efficiencies.

摘要

在自由基光聚合反应(RPPs)中,由于活性自由基的快速终止,光照停止后转化率会迅速达到平稳状态,这限制了RPPs在涉及光入射不均匀的应用中的更广泛使用,包括那些光传输衰减或表面不规则的应用。基于我们最近关于一种自由基暗固化光引发剂(DCPI)的报道,该引发剂通过在合适的氧化剂存在下利用光释放的胺实现潜在的氧化还原引发,从而在光照停止后继续聚合反应,我们开发了一种新的DCPI,其吸收光谱很好地延伸到了可见光范围。我们的设计过程涉及对候选分子的一系列计算研究,包括对取代基及其位置依赖性对吸收特性、电子跃迁、光化学机理及其相关能量学的系统研究。我们的量子化学计算确定了目标化合物5,7-二甲氧基-6-溴-3-芳酰基香豆素-DMPT/BPh,并预测它将通过在可见光照射下同时产生光自由基和光诱导释放高效氧化还原还原剂来促进暗固化机理。然后合成了这种连接有还原剂的发色团并用紫外-可见光谱对其进行了光学表征,结果表明它在405 nm处具有5710 M cm的摩尔吸光率,在455 nm处具有50 M cm的摩尔吸光率,对可见光有强烈吸收。然后我们证明了,在用455 nm发光二极管照射使稳定的单组分体系短暂活化后,在25分钟内额外转化率超过35%的广泛暗固化,在转化率达到20%时停止照射。相比之下,在同一时间点对对照配方进行遮光照射会导致转化率立即停止,在20%时达到平稳状态。我们确定了2.82的显著引发剂效率,这是由额外的氧化还原产生的自由基以及77%的光还原剂产生量子产率导致的。这种新型可见光DCPI优异的光固化和暗固化效率的结合,有望在RPP中开辟新的应用机会,特别是那些涉及高透光衰减树脂、具有产生不均匀辐照度的不规则特征表面以及在光活化步骤下游继续暗固化可提高生产线效率的生产线的应用。

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