Lactate anion catalyzes aminolysis of polyesters with anilines

Author:

Wu Fengtian12ORCID,Wang Yuepeng13,Zhao Yanfei13ORCID,Tang Minhao13,Zeng Wei13,Wang Ying13,Chang Xiaoqian13,Xiang Junfeng1ORCID,Han Buxing13ORCID,Liu Zhimin13ORCID

Affiliation:

1. Beijing National Laboratory for Molecular Sciences, Key Laboratory of Colloid and Interface and Thermodynamics, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.

2. Jiangxi Province Key Laboratory of Polymer Micro/Nano Manufacturing and Devices, Jiangxi Province Key Laboratory of Synthetic Chemistry, East China University of Technology, Nanchang 330013, China.

3. University of Chinese Academy of Sciences, Beijing 100049, China.

Abstract

Chemical transformation of spent polyesters into value-added chemicals is substantial for sustainable development but still challenging. Here, we report a simple, metal-free, and efficient aminolysis strategy to upcycle polylactic acid by anilines over lactate-based ionic liquids (e.g., tetrabutylammonium lactate), accessing a series of N -aryl lactamides under mild conditions. This strategy is also effective for degradation of poly(bisphenol A carbonate), affording bisphenol A and corresponding diphenylurea derivatives. It is found that, with the assistance of water, lactate anion as hydrogen-bond donor can efficiently activate carbonyl C atom of polyesters via hydrogen bonding with carbonyl O atom; meanwhile, as hydrogen-bond acceptor, it can enhance nucleophilicity of the N atom of anilines via hydrogen bonding with amino H atom. The nucleophilic attack of N atom of anilines on carbonyl C atom of polyesters results in cleavage of C─O bond of polymers and formation of the target products.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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