Interplay of Olefin Metathesis and Multiple Hydrogen Bonding Interactions: Covalently Cross-linked Zippers

被引:21
|
作者
Zeng, Jisen [1 ]
Wang, Wei [1 ]
Deng, Pengchi [1 ]
Feng, Wen [1 ]
Zhou, Jingjing [1 ]
Yang, Yuanyou [1 ]
Yuan, Lihua [1 ]
Yamato, Kazuhiro [2 ]
Gong, Bing [2 ]
机构
[1] Sichuan Univ, Inst Nucl Sci & Technol, Analyt & Testing Ctr, Coll Chem,Key Lab Radiat Phys & Technol,Minist Ed, Chengdu 610064, Peoples R China
[2] SUNY Buffalo, Dept Chem, Buffalo, NY 14260 USA
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
BONDED MOLECULAR DUPLEXES; RING-CLOSING METATHESIS; SUPRAMOLECULAR POLYMERS; HIGH-FIDELITY; RECOGNITION; COPOLYMERS; FOLDAMERS; DISCRETE; MOTIFS; MEDIA;
D O I
10.1021/ol201282d
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Hydrogen-bonded zippers bearing terminal alkene groups were treated with Grubbs' catalyst, leading to covalently cross-linked zippers without violating H-bonding sequence specificity. The yield of a cross-linked zipper depended on the stability of its H-bonded precursor, with a weakly associating pair giving reasonable yields only at high concentrations while strongly associating pairs showed nearly quantitative yields. The Integration of thermodynamic (H-bonding) and kinetic (irreversible C=C bond formation) processes suggests the possibility of developing many different covalent association units for constructing molecular structures based on a self-assembling way.
引用
收藏
页码:3798 / 3801
页数:4
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