TY - JOUR
T1 - Advancing Recyclable Thermosets through C═C/C═N Dynamic Covalent Metathesis Chemistry
AU - Zheng, Jie
AU - Feng, Hongzhi
AU - Zhang, Xinglong
AU - Zheng, Jianwei
AU - Ng, Jeffrey Kang Wai
AU - Wang, Sheng
AU - Hadjichristidis, Nikos
AU - Li, Zibiao
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/8/7
Y1 - 2024/8/7
N2 - Thermoset polymers have become integral to our daily lives due to their exceptional durability, making them feasible for a myriad of applications; however, this ubiquity also raises serious environmental concerns. Covalent adaptable networks (CANs) with dynamic covalent linkages that impart efficient reprocessability and recyclability to thermosets have garnered increasing attention. While various dynamic exchange reactions have been explored in CANs, many rely on the stimuli of active nucleophilic groups and/or catalysts, introducing performance instability and escalating the initial investment. Herein, we propose a new direct and catalyst-free C═C/C═N metathesis reaction between α-cyanocinnamate and aldimine as a novel dynamic covalent motif for constructing recyclable thermosets. This chemistry offers mild reaction conditions (room temperature and catalyst-free), ensuring high yields and simple isolation procedures. By incorporating dynamic C═C/C═N linkages into covalently cross-linked polymer networks, we obtained dynamic thermosets that exhibit both malleability and reconfigurability. The resulting tunable dynamic properties, coupled with the high thermal stability and recyclability of the C═C/C═N linkage-based networks, enrich the toolbox of dynamic covalent chemistry.
AB - Thermoset polymers have become integral to our daily lives due to their exceptional durability, making them feasible for a myriad of applications; however, this ubiquity also raises serious environmental concerns. Covalent adaptable networks (CANs) with dynamic covalent linkages that impart efficient reprocessability and recyclability to thermosets have garnered increasing attention. While various dynamic exchange reactions have been explored in CANs, many rely on the stimuli of active nucleophilic groups and/or catalysts, introducing performance instability and escalating the initial investment. Herein, we propose a new direct and catalyst-free C═C/C═N metathesis reaction between α-cyanocinnamate and aldimine as a novel dynamic covalent motif for constructing recyclable thermosets. This chemistry offers mild reaction conditions (room temperature and catalyst-free), ensuring high yields and simple isolation procedures. By incorporating dynamic C═C/C═N linkages into covalently cross-linked polymer networks, we obtained dynamic thermosets that exhibit both malleability and reconfigurability. The resulting tunable dynamic properties, coupled with the high thermal stability and recyclability of the C═C/C═N linkage-based networks, enrich the toolbox of dynamic covalent chemistry.
UR - http://www.scopus.com/inward/record.url?scp=85199488261&partnerID=8YFLogxK
U2 - 10.1021/jacs.4c05346
DO - 10.1021/jacs.4c05346
M3 - Article
C2 - 39046371
AN - SCOPUS:85199488261
SN - 0002-7863
VL - 146
SP - 21612
EP - 21622
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 31
ER -