Trifluoromethyl acting as stopper in [2]rotaxane

Suvankar Dasgupta; Kuo-Wei Huang; Jishan Wu

doi:10.1039/c2cc31009k

Trifluoromethyl acting as stopper in [2]rotaxane

Suvankar Dasgupta, Kuo-Wei Huang, Jishan Wu

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18 Scopus citations

Abstract

A modified dumbbell obtained by replacing one of the phenyl groups of the dibenzylammonium with a strong electron-withdrawing trifluoromethyl group templated the synthesis of the smallest [2]rotaxane reported so far. The trifluoromethyl group not only enhances the templating effect of the dumbbell but also acts as the stopper to prevent dethreading of a [20]crown ether macrocycle. © 2012 The Royal Society of Chemistry.

Original language	English (US)
Pages (from-to)	4821
Journal	Chemical Communications
Volume	48
Issue number	40
DOIs	https://doi.org/10.1039/c2cc31009k
State	Published - Mar 24 2012

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https://repository.kaust.edu.sa/bitstream/10754/235442/1/Trifluoromethyl%20acting%20as%20stopper%20in%20%5b2%5drotaxanew.pdf

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abstract = "A modified dumbbell obtained by replacing one of the phenyl groups of the dibenzylammonium with a strong electron-withdrawing trifluoromethyl group templated the synthesis of the smallest [2]rotaxane reported so far. The trifluoromethyl group not only enhances the templating effect of the dumbbell but also acts as the stopper to prevent dethreading of a [20]crown ether macrocycle. {\textcopyright} 2012 The Royal Society of Chemistry.",

author = "Suvankar Dasgupta and Kuo-Wei Huang and Jishan Wu",

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doi = "10.1039/c2cc31009k",

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AU - Dasgupta, Suvankar

AU - Huang, Kuo-Wei

AU - Wu, Jishan

N1 - KAUST Repository Item: Exported on 2020-10-01

PY - 2012/3/24

Y1 - 2012/3/24

N2 - A modified dumbbell obtained by replacing one of the phenyl groups of the dibenzylammonium with a strong electron-withdrawing trifluoromethyl group templated the synthesis of the smallest [2]rotaxane reported so far. The trifluoromethyl group not only enhances the templating effect of the dumbbell but also acts as the stopper to prevent dethreading of a [20]crown ether macrocycle. © 2012 The Royal Society of Chemistry.

AB - A modified dumbbell obtained by replacing one of the phenyl groups of the dibenzylammonium with a strong electron-withdrawing trifluoromethyl group templated the synthesis of the smallest [2]rotaxane reported so far. The trifluoromethyl group not only enhances the templating effect of the dumbbell but also acts as the stopper to prevent dethreading of a [20]crown ether macrocycle. © 2012 The Royal Society of Chemistry.

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VL - 48

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JO - Chemical Communications

JF - Chemical Communications

IS - 40

ER -

Trifluoromethyl acting as stopper in [2]rotaxane

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