Sequentially Hetero-functional, Topological Polymers by Step-growth Thiol-yne Approach

被引:40
作者
Han, Jin [1 ]
Zheng, Yaochen [1 ,2 ]
Zhao, Bo [1 ]
Li, Sipei [1 ]
Zhang, Yuanchao [1 ]
Gao, Chao [1 ]
机构
[1] Zhejiang Univ, MOE Key Lab Macromol Synth & Functionalizat, Dept Polymer Sci & Engn, Hangzhou 310027, Zhejiang, Peoples R China
[2] Yantai Univ, Coll Chem & Chem Engn, Yantai 264005, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
DNA-TEMPLATED POLYMERIZATION; HYPERBRANCHED POLYMERS; SEQUENCE; COPOLYMERS; EFFICIENT;
D O I
10.1038/srep04387
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Sequence-controlled polymers (SCPs) such as DNA and proteins play an important role in biology. Many efforts have been devoted to synthesize SCPs in the past half a century. However, to our knowledge, the artificial sequences containing independently functional groups have never been reported. Here, we present a facile and scalable approach based on radical-initiated step-growth polymerization to synthesize sequence-controlled functional polymers (SCFPs) with various topologies, covering from linear to random and hyperbranched polymers. The functional groups, such as OH/NH2, OH/COOH, and NH2/N-3, alternately arranged along the chain, which were further selectively functionalized to achieve DNA-mimic and hetero-multifunctional SCPs. This user-friendly strateg y exhibits advantages of commercially available monomers, catalyst-free process, fast reaction, high yield and water solvent, opening a general approach to facile and scalable synthesis of SCFPs.
引用
收藏
页数:8
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