Photocatalytic Direct Decarboxylation of Carboxylic Acids to Derivatize or Degrade Polymers

被引:59
|
作者
Adili, Alafate [1 ]
Korpusik, Angie B. [2 ]
Seidel, Daniel [1 ]
Sumerlin, Brent S. [2 ]
机构
[1] Univ Florida, Ctr Heterocycl Cpds, Dept Chem, Gainesville, FL 32611 USA
[2] Univ Florida, Ctr Macromol Sci & Engn, Dept Chem, George & Josephine Butler Polymer Res Lab, Gainesville, FL 32611 USA
基金
美国国家科学基金会;
关键词
Acridine; Decarboxylation; Degradation; Photocatalysis; Polymers; RING-OPENING POLYMERIZATION; POLAR MONOMERS; COPOLYMERIZATION; OLEFINS; LIMITATIONS; ETHYLENE;
D O I
10.1002/anie.202209085
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Visible light-mediated direct decarboxylation of carboxylic acids with an acridine photocatalyst is a convenient and powerful method to generate carbon-centered radicals in polymer chains. Advantageously, this process proceeds under mild conditions, without preactivation of the acid groups. We utilize decarboxylation in the presence of a hydrogen atom donor to form statistical acrylate-ethylene and acrylate-propylene copolymers, which are challenging to obtain by direct polymerization. We additionally show that decarboxylation of methacrylic acid units within polymethacrylates can trigger degradation of the polymer backbones. Moreover, a dual catalytic approach, which combines the function of an acridine photocatalyst with that of a cobaloxime catalyst, is leveraged to furnish unique copolymers with pendent alkenes. Our work indicates that direct decarboxylation is a versatile technique for the synthesis of functional materials with tailored compositions and properties.
引用
收藏
页数:7
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