Threading of three rings on two stations: a convergent approach to [4]rotaxane

A novel approach to efficient and selective construction of [4]rotaxane was proposed to demonstrate the superiority of H-bonded azo-macrocycles in forging higher order rotaxanes. The single crystal structure reveals the importance of the interplay of multiple non-covalent bonding interactions, parti...

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Published inChemical communications (Cambridge, England) Vol. 57; no. 99; pp. 1356 - 1359
Main Authors Zhou, Yidan, Wu, Jinyang, Liu, Zejiang, Xu, Weitao, Liu, Menglong, Jia, Along, Liu, Yuchen, Xiao, Xin, Li, Xiaowei, Yuan, Lihua
Format Journal Article
LanguageEnglish
Published England Royal Society of Chemistry 14.12.2021
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Summary:A novel approach to efficient and selective construction of [4]rotaxane was proposed to demonstrate the superiority of H-bonded azo-macrocycles in forging higher order rotaxanes. The single crystal structure reveals the importance of the interplay of multiple non-covalent bonding interactions, particularly π-stacking interactions, in stabilizing the host-guest complex. This may open an avenue to the synthesis of oligomeric mechanically interlocked molecules containing fewer stations but more rings. A novel approach to efficient and selective synthesis of [4]rotaxane with two stations was proposed to demonstrate the superiority of H-bonded azo-macrocycles in forging higher order rotaxanes.
Bibliography:10.1039/d1cc05501a
1
For ESI and crystallographic data in CIF or other electronic format see DOI
Electronic supplementary information (ESI) available: Further details of synthesis, characterization
H and 2D NMR experiments and computational modelling. CCDC
2111239
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1359-7345
1364-548X
DOI:10.1039/d1cc05501a