Coskun Halil Ibrahim, De Luca Bossa Ferdinando, Hu Xiaolei, Jockusch Steffen, Sobieski Julian, Yilmaz Gorkem, Matyjaszewski Krzysztof
Department of Chemistry, Carnegie Mellon University, 4400 Fifth Avenue, Pittsburgh, Pennsylvania 15213, United States.
Department of Chemistry and Center for Photochemical Sciences, Bowling Green State University, Bowling Green, Ohio 43403, United States.
J Am Chem Soc. 2024 Oct 23;146(42):28994-29005. doi: 10.1021/jacs.4c09927. Epub 2024 Oct 10.
In atom transfer radical polymerization (ATRP), dormant alkyl halides are intermittently activated to form growing radicals in the presence of a Cu/L/X-Cu/L (activator/deactivator) catalytic system. Recently developed very active copper complexes could decrease the catalyst concentration to ppm level. However, unavoidable radical termination results in irreversible oxidation of the activator to the deactivator species, leading to limited monomer conversions. Therefore, successful ATRP at a low catalyst loading requires continuous regeneration of the activators. Such a regenerative ATRP can be performed with various reducing agents under milder reaction conditions and with catalyst concentrations diminished in comparison to conventional ATRP. Photoinduced ATRP (PhotoATRP) is one of the most efficient methods of activator regeneration. It initially employed UV irradiation to reduce the air-stable excited X-Cu/L deactivators to the activators in the presence of sacrificial electron donors. Photocatalysts (PCs) can be excited after absorbing light at longer wavelengths and, due to their favorable redox potentials, can reduce X-Cu/L to Cu/L. Herein, we present the application of three commercially available xanthene dyes as ATRP PCs: rose bengal (RB), rhodamine B (RD), and rhodamine 6G (RD-6G). Even at very low Cu catalyst concentrations (50 ppm), they successfully controlled PhotoATRP. Well-defined polymers with preserved livingness were prepared under green LED irradiation, with subppm concentrations ([PC] ≥ 10 ppb) of RB and RD-6G or 5 ppm of RD. Interestingly, these PCs efficiently controlled ATRP at wavelengths longer than their absorption maxima but required higher loadings. Polymerizations proceeded with high initiation efficiencies, yielding polymers with narrow molecular weight distributions and high chain-end fidelity. UV-vis, fluorescence, and laser flash photolysis studies helped to elucidate the mechanism of the processes involved in the dual-catalytic systems, comprising parts per million of Cu complexes and parts per billion of PCs.
在原子转移自由基聚合(ATRP)中,在Cu/L/X-Cu/L(活化剂/钝化剂)催化体系存在下,休眠的卤代烷会间歇性地活化形成增长自由基。最近开发的活性非常高的铜配合物能够将催化剂浓度降低到ppm水平。然而,不可避免的自由基终止会导致活化剂不可逆地氧化为钝化剂物种,从而导致单体转化率受限。因此,在低催化剂负载量下成功进行ATRP需要活化剂的连续再生。这种再生ATRP可以在比传统ATRP更温和的反应条件下,使用各种还原剂进行,且催化剂浓度降低。光引发原子转移自由基聚合(PhotoATRP)是活化剂再生最有效的方法之一。它最初采用紫外线照射,在牺牲电子供体存在下,将空气稳定的激发态X-Cu/L钝化剂还原为活化剂。光催化剂(PCs)在吸收更长波长的光后可以被激发,并且由于其有利的氧化还原电位,可以将X-Cu/L还原为Cu/L。在此,我们展示了三种市售的呫吨染料作为ATRP光催化剂的应用:孟加拉玫瑰红(RB)、罗丹明B(RD)和罗丹明6G(RD-6G)。即使在非常低的铜催化剂浓度(50 ppm)下,它们也成功地控制了PhotoATRP。在绿色LED照射下,使用亚ppm浓度([PC]≥10 ppb)的RB和RD-6G或5 ppm的RD制备了具有保留活性的结构明确的聚合物。有趣的是,这些光催化剂在比其吸收最大值更长的波长下有效地控制了ATRP,但需要更高的负载量。聚合反应具有高引发效率,得到分子量分布窄且链端保真度高的聚合物。紫外可见光谱、荧光光谱和激光闪光光解研究有助于阐明双催化体系中所涉及过程的机理,该体系包含百万分之几的铜配合物和十亿分之几的光催化剂。