Immobilization of calix[4]arene-based glycoclusters on TiO2 nanoparticles via click Cu(I)-catalyzed azide–alkyne coupling

Lisa Moni; Stefano Rossetti; Marco Scoponi; Alberto Marra; Alessandro Dondoni

doi:10.1039/B919353G

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Chemical Communications

Issue 3, 2010

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Immobilization of calix[4]arene-based glycoclusters on TiO₂ nanoparticles via click Cu(I)-catalyzed azide–alkyne coupling

Lisa Moni , Stefano Rossetti , Marco Scoponi , Alberto Marra and Alessandro Dondoni

Chem. Commun., 2010, 46, 475-477

DOI: 10.1039/B919353G
Received 16 Sep 2009, Accepted 30 Oct 2009
First published on the web 16 Nov 2009

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Abstract
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We present the first type of tetraazide-functionalized calix[4]arene TiO₂ nanoparticles and their coupling to propargyl glycosides under Cu(I)-catalysis (click reaction), resulting in the immobilization of calix[4]arene-based glycoclusters on the TiO₂ surface.

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Syntheses and characterization data of all newcompounds
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Articles By

Lisa Moni
Stefano Rossetti
Marco Scoponi
Alberto Marra
Alessandro Dondoni

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Chemical Communications

Immobilization of calix[4]arene-based glycoclusters on TiO₂ nanoparticles via click Cu(I)-catalyzed azide–alkyne coupling

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