Noncovalent Interaction-Catalyzed High Conversion of Waste PET Plastics into Organic Esters under Mild Conditions

Abstract Herein, we report a versatile esterolysis strategy, driven by noncovalent interactions (such as hydrogen bonding and electrostatic forces), that depolymerizes waste poly(ethylene terephthalate) (PET) into high-value molecular precursors under mild conditions. This strategy can be applied to a broad range of ester substrates, including carboxylates, carbonates, and silicon/titanium (Si/Ti)-based esters. A series of mechanistic studies reveal that the TBD catalyst serves a dual function. It catalyzes the in situ generation of methanol from dimethyl carbonate while simultaneously driving the cleavage of C–O bonds in PET via hydrogen bonding and electrostatic interactions. Ultimately, this work establishes a widely applicable and sustainable platform for PET upcycling, which not only enhances the valorization of plastic waste but also provides a scalable solution to the global plastic pollution crisis.

Authors

Institutions

Publication Details

Journal
Organic Letters
Published
2026-09-09
DOI
https://doi.org/10.1021/acs.orglett.6c03149
Primary Topic
Carbon dioxide utilization in catalysis
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Noncovalent Interaction-Catalyzed High Conversion of Waste PET Plastics into Organic Esters under Mild Conditions

Ni Xiong, Guoyuan Yuan, Junjie Chen, Bolin Wang et al.
Organic Letters
Carbon dioxide utilization in catalysis
article

Noncovalent Interaction-Catalyzed High Conversion of Waste PET Plastics into Organic Esters under Mild Conditions

Ni Xiong, Guoyuan Yuan, Junjie Chen, Bolin Wang, Chen Zeng, Chunhong Hu, Xiaoyu Wu
article en

Abstract

Abstract Herein, we report a versatile esterolysis strategy, driven by noncovalent interactions (such as hydrogen bonding and electrostatic forces), that depolymerizes waste poly(ethylene terephthalate) (PET) into high-value molecular precursors under mild conditions. This strategy can be applied to a broad range of ester substrates, including carboxylates, carbonates, and silicon/titanium (Si/Ti)-based esters. A series of mechanistic studies reveal that the TBD catalyst serves a dual function. It catalyzes the in situ generation of methanol from dimethyl carbonate while simultaneously driving the cleavage of C–O bonds in PET via hydrogen bonding and electrostatic interactions. Ultimately, this work establishes a widely applicable and sustainable platform for PET upcycling, which not only enhances the valorization of plastic waste but also provides a scalable solution to the global plastic pollution crisis.

Organic Letters
Chongqing University of Science and Technology (CN), Henan University of Technology (CN), Xi'an Jiaotong University (CN)
Responsible consumption and production
Openalex Percentile: Top 24%
Carbon dioxide utilization in catalysis
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.