Hydrogenative Depolymerization of Nylons

被引:138
作者
Kumar, Amit [1 ]
von Wolff, Niklas [2 ]
Rauch, Michael [1 ]
Zou, You-Quan [1 ]
Shmul, Guy [3 ]
Ben-David, Yehoshoa [3 ]
Leitus, Gregory [3 ]
Avram, Liat [3 ]
Milstein, David [1 ]
机构
[1] Weizmann Inst Sci, Dept Organ Chem, IL-76100 Rehovot, Israel
[2] Univ Paris, CNRS, UMR 7591, Lab Electrochim Mol, F-75013 Paris, France
[3] Weizmann Inst Sci, Dept Chem Res Support, IL-76100 Rehovot, Israel
基金
欧洲研究理事会;
关键词
CATALYTIC-HYDROGENATION; SELECTIVE HYDROGENATION; CYCLIC IMIDES; AMIDES; ALCOHOLS; AMINES; CO2; DESYMMETRIZATION; LIBERATION; MECHANISM;
D O I
10.1021/jacs.0c05675
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The widespread crisis of plastic pollution demands discovery of new and sustainable approaches to degrade robust plastics such as nylons. Using a green and sustainable approach based on hydrogenation, in the presence of a ruthenium pincer catalyst at 150 degrees C and 70 bar H-2, we report here the first example of hydrogenative depolymerization of conventional, widely used nylons and polyamides, in general. Under the same catalytic conditions, we also demonstrate the hydrogenation of a polyurethane to produce diol, diamine, and methanol. Additionally, we demonstrate an example where monomers (and oligomers obtained from the hydrogenation process can be dehydrogenated back to a poly(oligo)amide of approximately similar molecular weight, thus completing a closed loop cycle for recycling of polyamides. Based on the experimental and density functional theory studies, we propose a catalytic cycle for the process that is facilitated by metal-ligand cooperativity. Overall, this unprecedented transformation, albeit at the proof of concept level, offers a new approach toward a cleaner route to recycling nylons.
引用
收藏
页码:14267 / 14275
页数:9
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