CH⋅⋅⋅O Hydrogen Bonding Induced Triazole Foldamers: Efficient Halogen Bonding Receptors for Organohalogens | Zendy

You LiYan | Zendy; Chen ShiGui | Zendy; Zhao Xin | Zendy; Liu Yi | Zendy; Lan WenXian | Zendy; Zhang Ying | Zendy; Lu HaoJie | Zendy; Cao ChunYang | Zendy; Li ZhanTing | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

CH⋅⋅⋅O Hydrogen Bonding Induced Triazole Foldamers: Efficient Halogen Bonding Receptors for Organohalogens

Author(s) -

You LiYan,

Chen ShiGui,

Zhao Xin,

Liu Yi,

Lan WenXian,

Zhang Ying,

Lu HaoJie,

Cao ChunYang,

Li ZhanTing

Publication year - 2012

Publication title -

angewandte chemie international edition

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 5.831

H-Index - 550

eISSN - 1521-3773

pISSN - 1433-7851

DOI - 10.1002/anie.201106996

Subject(s) - intramolecular force , hydrogen bond , halogen bond , triazole , halogen , chemistry , ring (chemistry) , crystallography , combinatorial chemistry , stereochemistry , molecule , organic chemistry , alkyl

Into the fold : Intramolecular CH⋅⋅⋅O hydrogen bonding has been utilized to create new aromatic triazole foldamers. Remarkably, all the triazole units of the foldamers are guided to orientate inward to form a nitrogen ring. As a result, they can efficiently bind neutral tri‐ and didentate organohalogens through multiple N⋅⋅⋅X (X=Cl, Br, I) halogen bonds to form stable 1:1 complexes.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research