A series of azido-dyes were synthesized through Knoevenagel reactions of an azido-BODIPY with aromatic aldehydes. The nature of the substituents allowed the fine tuning of their spectroscopic properties. The dyes were used to decorate oxidized multiwalled carbon nanotubes (ox-MWCNTs), bearing terminal triple bond groups, by CuAAC reactions, affording fluorescent materials. This decoration allowed the efficient determination of the internalization of the ox-MWCNT derivatives by different model cancer cells, such as MCF7.

Azido-Substituted BODIPY Dyes for the Production of Fluorescent Carbon Nanotubes

Giambastiani Giuliano;Tuci Giulia;
2015

Abstract

A series of azido-dyes were synthesized through Knoevenagel reactions of an azido-BODIPY with aromatic aldehydes. The nature of the substituents allowed the fine tuning of their spectroscopic properties. The dyes were used to decorate oxidized multiwalled carbon nanotubes (ox-MWCNTs), bearing terminal triple bond groups, by CuAAC reactions, affording fluorescent materials. This decoration allowed the efficient determination of the internalization of the ox-MWCNT derivatives by different model cancer cells, such as MCF7.
2015
Istituto di Chimica dei Composti OrganoMetallici - ICCOM -
BODIPY
carbon nanotubes
click reaction
fluorescent probes
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/306235
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