RETRACTED: Catalytic living ring-opening metathesis polymerization (Retracted article. See vol. 10, pg. 573, 2018)

被引:0
|
作者
Nagarkar, Amit A. [1 ]
Kilbinger, Andreas F. M. [1 ]
机构
[1] Univ Fribourg, Dept Chem, CH-1700 Fribourg, Switzerland
基金
瑞士国家科学基金会;
关键词
HCV PROTEASE INHIBITOR; CATHEPSIN K-INHIBITOR; RUTHENIUM BY-PRODUCTS; LARGE-SCALE SYNTHESIS; OLEFIN METATHESIS; CLOSING METATHESIS; FUNCTIONALIZED POLY(NORBORNENE)S; RADICAL POLYMERIZATION; CONVENIENT METHOD; BLOCK-COPOLYMERS;
D O I
10.1038/NCHEM.2320
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In living ring-opening metathesis polymerization (ROMP), a transition-metal-carbene complex polymerizes ring-strained olefins with very good control of the molecular weight of the resulting polymers. Because one molecule of the initiator is required for each polymer chain, however, this type of polymerization is expensive for widespread use. We have now designed a chain-transfer agent (CTA) capable of reducing the required amount of metal complex while still maintaining full control over the living polymerization process. This new method introduces a degenerative transfer process to ROMP. We demonstrate that substituted cyclohexene rings are good CTAs, and thereby preserve the 'living' character of the polymerization using catalytic quantities of the metal complex. The resulting polymers show characteristics of a living polymerization, namely narrow molecular-weight distribution, controlled molecular weights and block copolymer formation. This new technique provides access to well-defined polymers for industrial, biomedical and academic use at a fraction of the current costs and significantly reduced levels of residual ruthenium catalyst.
引用
收藏
页码:718 / 723
页数:6
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