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BP23C7: high-yield synthesis and application in constructing [3]rotaxanes and responsive pseudo[2]rotaxanes.

Authors :
Prakashni M
Dasgupta S
Source :
Organic & biomolecular chemistry [Org Biomol Chem] 2024 Feb 28; Vol. 22 (9), pp. 1871-1884. Date of Electronic Publication: 2024 Feb 28.
Publication Year :
2024

Abstract

A biphenyl-23-crown-7 ether (BP23C7) is synthesized in 86% yield from commercially available starting materials. BP23C7 forms pseudo[2]rotaxane with a dibenzylammonium ion (DBA <superscript>+</superscript> ), exhibiting a good association constant value ( k <subscript>a</subscript> = 1 × 10 <superscript>3</superscript> M <superscript>-1</superscript> ). Subsequently, fluorophoric properties of BP23C7 and anthracene terminated axles are blended to create responsive pseudo[2]rotaxanes. The "turn-on" fluorescence response of BP23C7 due to the addition of fluoride and chloride anions to pseudo[2]rotaxane systems has been investigated. Concomitant fluorescence quenching of the anthracene moiety of corresponding axles due to ion-pair formation has been addressed. Furthermore, two variants of [23]crown ethers, i.e. BP23C7 and o -xylene-23-crown-7 ether (X23C7), are applied for constructing homo[3]rotaxane architectures. A half-axle comprising of DBA <superscript>+</superscript> moiety and a terminal olefin is mixed separately with two [23]crown ethers and subjected to self-metathesis using Grubbs' first-generation catalyst.

Details

Language :
English
ISSN :
1477-0539
Volume :
22
Issue :
9
Database :
MEDLINE
Journal :
Organic & biomolecular chemistry
Publication Type :
Academic Journal
Accession number :
38349013
Full Text :
https://doi.org/10.1039/d3ob02094k