C-I•••π Halogen Bonding Driven Supramolecular Helix of Bilateral N-Amidothioureas Bearing β-Turns

被引:106
作者
Cao, Jinlian [1 ]
Yan, Xiaosheng [1 ]
He, Wenbin [1 ]
Li, Xiaorui [1 ]
Li, Zhao [1 ]
Mo, Yirong [2 ,3 ]
Liu, Maili [4 ]
Jiang, Yun-Bao [1 ]
机构
[1] Xiamen Univ, MOE Key Lab Spectrochem Anal & Instrumentat, Collaborat Innovat Ctr Chem Energy Mat IChEM, Dept Chem,Coll Chem & Chem Engn, Xiamen 361005, Peoples R China
[2] Xiamen Univ, Dept Chem, Coll Chem & Chem Engn, Xiamen 361005, Peoples R China
[3] Western Michigan Univ, Dept Chem, Kalamazoo, MI 49008 USA
[4] Chinese Acad Sci, Wuhan Inst Phys & Math, State Key Lab Magnet Resonance & Atom & Mol Phys, Wuhan 430071, Peoples R China
关键词
MAJORITY-RULES; RECOGNITION; COMPLEXES; CHIRALITY; PEPTIDES; PROTEINS; THIOUREA; BENZENE; STACKS; CHAINS;
D O I
10.1021/jacs.6b13171
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report the first example of C-I center dot center dot center dot pi halogen bonding driven supramolecular helix in highly dilute solution of micromolar concentration, using alanine based bilateral I-substituted N-amidothioureas that contain helical fragments, the beta-turn structures. The halogen bonding interactions afford head-to-tail linkages that help to propagate the helicity of the helical fragments. In support of this action of the halogen bonding, chiral amplification was observed in the supra molecular helix formed in acetonitrile solution. The present finding provides alternative tools in the design of self-assembling macromolecules.
引用
收藏
页码:6605 / 6610
页数:6
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