Journal
MACROMOLECULES
Volume 55, Issue 2, Pages 643-651Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.macromol.1c02130
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Funding
- National Natural Science Foundation of China [21801049]
- Opening Project of Key Laboratory of Polymer Processing Engineering (South China University of Technology)
- Ministry of Education [KFKT2006]
- King Abdullah University of Science and Technology
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A highly efficient and multicomponent step-growth polymerization via carbene intermediates is established by bimetallic relay catalytic systems. This method overcomes the limitation on the choice of carbene monomers and achieves high-molecular-weight polymers. The results suggest an untapped pathway for the use of metal carbene intermediates to construct new macromolecules.
A highly efficient and multicomponent step-growth polymerization via carbene intermediates is established by bimetallic relay catalytic systems. This strategy, which provides a facile synthetic pathway to novel luminescent polysulfonamides, could overcome the limitation on the choice of carbene monomers and their difficulty in achieving high-molecular-weight polymers. The polymerizations occur through a tandem Cu(I)-catalyzed click reaction and an Rh(II)-catalyzed carbene 1,3-insertion reaction. The high reactivity of Rh(II)-bonded imino carbene intermediates allows a wide range of reactivity with various carboxylic acids, alcohols, and phenols. These results point to an untapped pathway for the use of metal carbene intermediates to construct new macromolecules.
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