Department of Chemistry, Carnegie Mellon University, 4400 Fifth Avenue, Pittsburgh, Pennsylvania 15213, United States.
Faculty of Chemistry, University of Warsaw, Żwirki i Wigury 101, 02-089 Warsaw, Poland.
Acc Chem Res. 2021 Apr 6;54(7):1779-1790. doi: 10.1021/acs.accounts.1c00032. Epub 2021 Mar 22.
Atom-transfer radical polymerization (ATRP) is a well-known technique for the controlled polymerization of vinyl monomers under mild conditions. However, as with any other radical polymerization, ATRP typically requires rigorous oxygen exclusion, making it time-consuming and challenging to use by nonexperts. In this Account, we discuss various approaches to achieving oxygen tolerance in ATRP, presenting the overall progress in the field.Copper-mediated ATRP, which we first discovered in the late 1990s, uses a Cu/L activator that reversibly reacts with the dormant C(sp)-X polymer chain end, forming a X-Cu/L deactivator and a propagating radical. Oxygen interferes with activation and chain propagation by quenching the radicals and oxidizing the activator. At ATRP equilibrium, the activator is present at a much higher concentration than the propagating radicals. Thus, oxidation of the activator is the dominant inhibition pathway. In conventional ATRP, this reaction is irreversible, so oxygen must be strictly excluded to achieve good results.Over the last two decades, our group has developed several ATRP techniques based on the concept of regenerating the activator. When the oxidized activator is continuously converted back to its active reduced form, then the catalytic system itself can act as an oxygen scavenger. Regeneration can be accomplished by reducing agents and photo-, electro-, and mechanochemical stimuli. This family of methods offers a degree of oxygen tolerance, but most of them can tolerate only a limited amount of oxygen and do not allow polymerization in an open vessel.More recently, we discovered that enzymes can be used in auxiliary catalytic systems that directly deoxygenate the reaction medium and protect the polymerization process. We developed a method that uses glucose oxidase (GOx), glucose, and sodium pyruvate to very effectively scavenge oxygen and enable open-vessel ATRP. By adding a second enzyme, horseradish peroxidase (HPR), we managed to extend the role of the auxiliary enzymatic system to generating carbon-based radicals and changed ATRP from an oxygen-sensitive to an oxygen-fueled reaction.While performing control experiments for the enzymatic methods, we noticed that using sodium pyruvate under UV irradiation triggers polymerization without the presence of GOx. This serendipitous discovery allowed us to develop the first oxygen-proof, small-molecule-based, photoinduced ATRP system. It has oxygen tolerance similar to that of the enzymatic methods, exhibits superior compatibility with both aqueous media and organic solvents, and avoids problems associated with purifying polymers from enzymes. The system was able to rapidly polymerize -isopropylacrylamide, a challenging monomer, with a high degree of control.These contributions have substantially simplified the use of ATRP, making it more practical and accessible to everyone.
原子转移自由基聚合(ATRP)是一种在温和条件下可控聚合乙烯基单体的知名技术。然而,与任何其他自由基聚合一样,ATRP 通常需要严格的氧气排除,这使得非专业人士使用起来既耗时又具有挑战性。在本综述中,我们讨论了实现 ATRP 氧耐受性的各种方法,展示了该领域的整体进展。
我们在 20 世纪 90 年代末首次发现的铜介导 ATRP 使用 Cu/L 活化剂与休眠的 C(sp)-X 聚合物链末端可逆反应,形成 X-Cu/L 失活剂和增长自由基。氧气通过猝灭自由基和氧化活化剂来干扰活化和链增长。在 ATRP 平衡时,活化剂的浓度远高于增长自由基。因此,活化剂的氧化是主要的抑制途径。在传统的 ATRP 中,这个反应是不可逆的,所以必须严格排除氧气才能取得好的结果。
在过去的二十年里,我们的小组基于再生活化剂的概念开发了几种 ATRP 技术。当氧化的活化剂被连续转化回其活性还原形式时,那么催化体系本身就可以充当氧气清除剂。再生可以通过还原剂和光、电和机械化学刺激来完成。这一系列方法提供了一定程度的氧气耐受性,但它们大多数只能耐受有限量的氧气,并且不允许在开放容器中聚合。
最近,我们发现酶可以在辅助催化体系中使用,直接脱氧反应介质并保护聚合过程。我们开发了一种使用葡萄糖氧化酶 (GOx)、葡萄糖和丙酮酸钠非常有效地清除氧气并实现开放容器 ATRP 的方法。通过添加第二种酶辣根过氧化物酶 (HPR),我们设法将辅助酶系统的作用扩展到生成碳基自由基,并将 ATRP 从氧气敏感反应转变为氧气燃料反应。
在进行酶法的对照实验时,我们注意到在紫外光照射下使用丙酮酸钠会引发聚合,而无需存在 GOx。这个偶然的发现使我们能够开发出第一个氧气证明、基于小分子的光诱导 ATRP 系统。它具有与酶法相似的氧气耐受性,与水相介质和有机溶剂都具有出色的相容性,并避免了从酶中纯化聚合物所带来的问题。该系统能够快速聚合 - 异丙基丙烯酰胺,这是一种具有挑战性的单体,具有高度的可控性。
这些贡献大大简化了 ATRP 的使用,使其更实用,更易于为所有人所接受。