Selective Lanthanide‐Organic Catalyzed Depolymerization of Nylon‐6 to ϵ‐Caprolactam

• Published in: Angewandte Chemie International Edition Vol. 62; no. 4; pp. e202212543 - n/a
• Main Authors: Wursthorn, Lukas, Beckett, Kristen, Rothbaum, Jacob O., Cywar, Robin M., Lincoln, Clarissa, Kratish, Yosi, Marks, Tobin J.
• Format: Journal Article
• Language: English
• Published: WEINHEIM Wiley 23.01.2023; Wiley Subscription Services, Inc
• Edition: International ed. in English
• Subjects: Caprolactam; Catalysts; Catalytic activity; Chemical Recycling; Chemistry; Chemistry, Multidisciplinary; Depolymerization; Green Chemistry; Hydrogen bonds; Lanthanides; Nylon; Physical Sciences; Plastic; Polyethylene terephthalate; Polymers; Polypropylene; Science & Technology; POLYMERS; ENERGY; Nylon; PLASTIC WASTE; Green Chemistry; Plastic; THERMAL-DEGRADATION; CIRCULAR ECONOMY; Chemical Recycling; POLYAMIDE 6; Lanthanides; KINETICS; PYROLYSIS; CYCLIC OLIGOMERS; PET
• ISSN: 1433-7851; 1521-3773
• DOI: 10.1002/anie.202212543

Nylon‐6 is selectively depolymerized to the parent monomer ϵ‐caprolactam by the readily accessible and commercially available lanthanide trisamido catalysts Ln(N(TMS)2)3 (Ln=lanthanide). The depolymerization process is solvent‐free, near quantitative, highly selective, and operates at the lowest Nylon‐6 to ϵ‐caprolactam depolymerization temperature reported to date. The catalytic activity of the different lanthanide trisamides scales with the Ln3+ ionic radius, and this process is effective with post‐consumer Nylon‐6 as well as with Nylon‐6+polyethylene, polypropylene or polyethylene terephthalate mixtures. Experimental kinetic data and theoretical (DFT) mechanistic analyses suggest initial deprotonation of a Nylon terminal amido N−H bond, which covalently binds the catalyst to the polymer, followed by a chain‐end back‐biting process in which ϵ‐caprolactam units are sequentially extruded from the chain end. Commercial and post‐consumer Nylon‐6 are selectively recycled to the ϵ‐caprolactam monomer in high yields by readily accessible lanthanide tris(amide) catalysts in a solvent‐free process. Catalytic activity scales with the lanthanide ionic radius. A chain‐end backbiting mechanism is proposed from experimental and theoretical analyses.