Flexible Porous Organic Polymers with α,β-Enone-Linkage via AlCl <sub>3</sub> -Catalyzed Horner–Wadsworth–Emmons Polymerization for Pd Recovery

In this work, highly porous organic polymers with α,β-enone-linkage were synthesized via the Horner–Wadsworth–Emmons (H-W-E) polymerization in 10–20 g, and the catalytic amount of AlCl 3 was found to increase the BET surface area of the as-prepared BIT-POP-120 and BIT-POP-121 dramatically (up to 716 m 2 g –1 ), much higher than that of enone-liked porous organic polymers (POPs) reported. More importantly, this H-W-E polymerization of triphsophonate 4 with 2,5-hexanedione 6 provided a powerful way to offer 18% flexible moiety in BIT-POP-121 based on low-field NMR. Very high Pd/Pt selectivity of 3.54 and 28 was observed for BIT-POP-121 respectively, based on the adsorption capacity and K d value using a binary solution of Pd 2+ and Pt 2+ . This is very promising for the Pd recovery from the spent automotive catalytic converters in the future. The powerful strategy for making flexible POPs by H–W-E polymerization using easily available and stable aliphatic diketones will lead the development of high-performance flexible POPs for broad applications including recovery of precious metals in the near future.

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Journal
ACS Macro Letters
Published
2026-06-30
DOI
https://doi.org/10.1021/acsmacrolett.6c00261
Primary Topic
Covalent Organic Framework Applications
Type
article
Field-Weighted Citation Impact
0.00

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article

Flexible Porous Organic Polymers with α,β-Enone-Linkage via AlCl 3 -Catalyzed Horner–Wadsworth–Emmons Polymerization for Pd Recovery

Xiang‐Guo Hu, Hanyuan Chen, Mu‐Hua Huang, Yue Wang et al.
ACS Macro Letters
Covalent Organic Framework Applications
article

Flexible Porous Organic Polymers with α,β-Enone-Linkage via AlCl 3 -Catalyzed Horner–Wadsworth–Emmons Polymerization for Pd Recovery

Xiang‐Guo Hu, Hanyuan Chen, Mu‐Hua Huang, Yue Wang, Boya Kuang, Y Huang, Ze-Rui Meng, Ze-Shuai Qi, Guo-Qing Ren
article en

Abstract

In this work, highly porous organic polymers with α,β-enone-linkage were synthesized via the Horner–Wadsworth–Emmons (H-W-E) polymerization in 10–20 g, and the catalytic amount of AlCl 3 was found to increase the BET surface area of the as-prepared BIT-POP-120 and BIT-POP-121 dramatically (up to 716 m 2 g –1 ), much higher than that of enone-liked porous organic polymers (POPs) reported. More importantly, this H-W-E polymerization of triphsophonate 4 with 2,5-hexanedione 6 provided a powerful way to offer 18% flexible moiety in BIT-POP-121 based on low-field NMR. Very high Pd/Pt selectivity of 3.54 and 28 was observed for BIT-POP-121 respectively, based on the adsorption capacity and K d value using a binary solution of Pd 2+ and Pt 2+ . This is very promising for the Pd recovery from the spent automotive catalytic converters in the future. The powerful strategy for making flexible POPs by H–W-E polymerization using easily available and stable aliphatic diketones will lead the development of high-performance flexible POPs for broad applications including recovery of precious metals in the near future.

ACS Macro Letters
Beijing Institute of Technology (CN), Advanced Materials Corporation (United States) (US), Chemical Synthesis Lab (SG), Jiangxi Normal University (CN)
National Natural Science Foundation of China, Beijing Municipal Natural Science Foundation
Openalex Percentile: Top 16%
Covalent Organic Framework Applications
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