King Eric R, Hunt Samuel B, Hamernik Levi J, Gonce Lauren E, Wiggins Jeffrey S, Azoulay Jason D
School of Polymer Science and Engineering, The University of Southern Mississippi, 118 College Drive, Hattiesburg, Mississippi 39406, United States.
JACS Au. 2021 Jul 21;1(9):1342-1347. doi: 10.1021/jacsau.1c00208. eCollection 2021 Sep 27.
Synthetic aromatic polymers are ubiquitous and indispensable to modern life, industry, and the global economy. The direct functionalization of these materials remains a considerable challenge on account of their unreactive aromatic C-H bonds and robust physical properties. Here, we demonstrate that homogeneous gold catalysis offers a mild, chemoselective, and practical approach to functionalize high-volume commodity aromatic polymers. Utilizing a gold-catalyzed intermolecular hydroarylation between a methyl ester functionalized alkyne, methyl propiolate, and nucleophilic arenes within polystyrene (PS) results in direct functionalization of phenyl rings with 1,2-substituted methyl acrylate functional groups. The reactivity and functionalization depend on the steric and electronic environment of the catalyst, counterion pairing, and method of activation. The reactivity is broad in scope, enabling the functionalization of arenes within commercial polysulfone (PSU) and waste polyethylene terephthalate (PET). These reactions open new opportunities to chemically transform aromatic polymers and modify their physical properties.
合成芳香族聚合物在现代生活、工业和全球经济中无处不在且不可或缺。由于这些材料中不活泼的芳香族碳氢键以及坚固的物理性质,其直接功能化仍然是一个巨大的挑战。在此,我们证明均相金催化为功能化大量商用芳香族聚合物提供了一种温和、化学选择性且实用的方法。利用金催化的分子间氢芳基化反应,在聚苯乙烯(PS)中,甲酯官能化的炔烃(丙酸甲酯)与亲核芳烃之间发生反应,使得苯环直接被1,2-取代的丙烯酸甲酯官能团功能化。反应活性和功能化取决于催化剂的空间和电子环境、抗衡离子配对以及活化方法。该反应活性范围广泛,能够实现商用聚砜(PSU)和废弃聚对苯二甲酸乙二酯(PET)中芳烃的功能化。这些反应为化学转化芳香族聚合物并改变其物理性质开辟了新的机会。