Direct Synthesis of Poly(adipate)Esters via Catalytic Isomerizing Dual Hydroesterificative Polymerization of 1,3‐Butadiene

S Shen Gao (Frontiers Science Center for Transformative Molecules, State Key Laboratory of Synergistic Chem-Bio Synthesis, Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, School of Chemistry and Chemical Engineering) L Lei Su X Xuehe Lu (Frontiers Science Center for Transformative Molecules, Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, State Key Laboratory of Synergistic Chem‐Bio Synthesis, School of Chemistry and Chemical Engineering Shanghai Jiao Tong University Shanghai 200240 China) H Huiwen Yang J Jiaming Zou (Frontiers Science Center for Transformative Molecules, State Key Laboratory of Synergistic Chem-Bio Synthesis, Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, School of Chemistry and Chemical Engineering) X Xi Yang S Shan Tang (Frontiers Science Center for Transformative Molecules, School of Chemistry and Chemical Engineering) J Jiawang Liu (Frontiers Science Center for Transformative Molecules, State Key Laboratory of Synergistic Chem-Bio Synthesis, Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, School of Chemistry and Chemical Engineering)

Abstract

Abstract Aliphatic polyesters, such as poly(adipate)esters, are attracting substantial attention as sustainable materials due to their degradability, recyclability, and versatility in various applications. However, the conventional production of poly(adipate)esters relies on energy‐intensive processes and petroleum‐derived adipic acid (AA), whose synthesis poses environmental concerns, including nitrous oxide emissions. Herein, we introduce a novel Pd‐catalyzed isomerizing dual hydroesterificative polymerization (IDHP) strategy for direct poly(adipate)ester synthesis from readily available feedstocks of 1,3‐butadiene, diols, and carbon monoxide. Key to success lay in the utilization of an electron‐rich phosphine ligand with bulky steric hindrance, which efficiently facilitated linear‐selective isomerizing hydroesterification. Mechanistic investigations revealed that the isomerizing hydroesterificative polymerization exhibited remarkable efficiency in producing poly(adipate)esters. The resulting poly(adipate)esters possess a similar structure compared to those produced by traditional polycondensation. With abundant feedstocks and atom‐economy, this methodology provides a practical and eco‐friendly approach to the production of poly(adipate)esters with varied microstructures.

Article Details

Volume / Issue Vol. 64, Issue 27
Published July 01, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (8)

S

Shen Gao

Frontiers Science Center for Transformative Molecules, State Key Laboratory of Synergistic Chem-Bio Synthesis, Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, School of Chemistry and Chemical Engineering

L

Lei Su

X

Xuehe Lu

Frontiers Science Center for Transformative Molecules, Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, State Key Laboratory of Synergistic Chem‐Bio Synthesis, School of Chemistry and Chemical Engineering Shanghai Jiao Tong University Shanghai 200240 China

H

Huiwen Yang

J

Jiaming Zou

Frontiers Science Center for Transformative Molecules, State Key Laboratory of Synergistic Chem-Bio Synthesis, Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, School of Chemistry and Chemical Engineering

X

Xi Yang

S

Shan Tang

Frontiers Science Center for Transformative Molecules, School of Chemistry and Chemical Engineering

J

Jiawang Liu

Frontiers Science Center for Transformative Molecules, State Key Laboratory of Synergistic Chem-Bio Synthesis, Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, School of Chemistry and Chemical Engineering