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A novel Pd-metalated porous organic phenanthroline-based polymer for heterogeneous cyanation of aryl halides.

Created on 20 Oct 2026

Authors

Xuan Lai, Sanqi Liang, Wu Zhang, Jie Lin, Jiale Huang, Shunmin Ding, Shengjun Deng

Published in

Dalton transactions (Cambridge, England : 2003). Oct 20, 2026. Epub Oct 20, 2026.

Abstract

The construction of porous organic phenanthroline-based polymers without functional groups is meaningful but also challenging, as they could offer a novel, single-site, stable platform for diverse catalytic applications. In this study, a unique strategy was devised to construct porous organic phenanthroline-based polymers (POP-Phen-X) without reactive/coordinating functional groups in the polymer skeleton. The polymers POP-Phen-X with high BET surface areas were synthesized using a solvent knitting Friedel-Crafts polymerization method. The well-defined and isolated phenanthroline sites of POP-Phen-X can serve as a platform for the immobilization of metal catalysts via coordination bonds. The post-synthetic metalation of POP-Phen-A with palladium(II) acetate afforded a selective heterogeneous Pd catalyst for the cyanation of aryl halides. The resulting Pd/POP-Phen-A exhibited effective catalytic performance towards the cyanation of aryl halides with a TON of 200 and good recyclability.

PMID:
42898041
Bibliographic data and abstract were imported from PubMed on 20 Oct 2026.

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