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Triazine-Carbon Nanotubes: New Platforms for the Design of Flavin Receptors.

Authors :
Lucío MI
Pichler F
Ramírez JR
de la Hoz A
Sánchez-Migallón A
Hadad C
Quintana M
Giulani A
Bracamonte MV
Fierro JL
Tavagnacco C
Herrero MA
Prato M
Vázquez E
Source :
Chemistry (Weinheim an der Bergstrasse, Germany) [Chemistry] 2016 Jun 20; Vol. 22 (26), pp. 8879-88. Date of Electronic Publication: 2016 May 11.
Publication Year :
2016

Abstract

The synthesis of functionalised carbon nanotubes as receptors for riboflavin (RBF) is reported. Carbon nanotubes, both single-walled and multi-walled, have been functionalised with 1,3,5-triazines and p-tolyl chains by aryl radical addition under microwave irradiation and the derivatives have been fully characterised by using a range of techniques. The interactions between riboflavin and the hybrids were analysed by using fluorescence and UV/Vis spectroscopic techniques. The results show that the attached functional groups minimise the π-π stacking interactions between riboflavin and the nanotube walls. Comparison of p-tolyl groups with the triazine groups shows that the latter have stronger interactions with riboflavin because of the presence of hydrogen bonds. Moreover, the triazine derivatives follow the Stern-Volmer relationship and show a high association constant with riboflavin. In this way, artificial receptors in catalytic processes could be designed through specific control of the interaction between functionalised carbon nanotubes and riboflavin.<br /> (© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Details

Language :
English
ISSN :
1521-3765
Volume :
22
Issue :
26
Database :
MEDLINE
Journal :
Chemistry (Weinheim an der Bergstrasse, Germany)
Publication Type :
Academic Journal
Accession number :
27168484
Full Text :
https://doi.org/10.1002/chem.201600630