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Program Scientific Program
POS1-1665

Controlled C–N Bond Construction in Polymers via Post-Polymerization Amidation Strategies

Topic

S1. Polymer Synthesis

When and Where

Sep 30, 2026   08:30 - 09:30
Room 301 (Grand Ballroom)

Session Chairs

Heesuk KIM
Jinhye BAE

Presenter(s)

Seung Beom Baek (Institute for Basic Science)

Co-Author(s)

Beomsoon Park (Institute for Basic Science), Youngho Kim (Korea Advanced Institute of Science and Technology), Myungeun Seo (Korea Advanced Institute of Science and Technology), Sukbok Chang (Institute for Basic Science)

Abstract

Post-polymerization modification (PPM) offers a versatile platform for introducing chemical functionality into established polymer architectures, providing opportunities to tailor polymer properties beyond the structural constraints of conventional polymer synthesis. However, achieving efficient functionalization while maintaining the structural integrity and molecular characteristics of the parent polymer remains a fundamental challenge.

Herein, we investigate amidation-based strategies for the controlled construction of C–N bonds in diverse polymer architectures. By exploiting complementary chemical reactivities of polymer backbones and functional groups, selective incorporation of amide functionalities can be achieved under mild reaction conditions. The developed approaches enable molecular-level modification of polymers while minimizing undesired structural changes, providing access to functionalized materials with tunable chemical and physical properties.

In this work, two complementary approaches are explored for C–N bond construction through post-polymerization amidation. The first approach enables the direct amidation of C–H bonds within polyether backbones, providing a means to introduce nitrogen-containing functionalities at otherwise inert polymer sites while preserving the underlying polymer structure. The second approach utilizes decarboxylative amidation of carboxylic acid-functionalized polymers, enabling the conversion of pre-installed functional groups into amide functionalities with controlled degrees of modification. Together, these strategies highlight the versatility of amidation chemistry for molecular-level diversification of polymer structures and provide insights into balancing functionalization efficiency, chemoselectivity, and preservation of polymer molecular architecture.
Supported by
Korea Tourism Organization BUSAN TOURISM ORGANIZATION
Sponsored by
DONGWOO FINE-CHEM Co., Ltd. Korea Research Institute of Chemical Technology Advanced Materials Division Sejin CI DONGJIN SEMICHEM HAEDONG SCIENCE FOUNDATION COSMAX EcoProBM Young Eng. Sci. Doosan SAMSUNG SDI S-OIL 한국도레이과학진흥재단