Triazine‐Carbon Nanotubes: New Platforms for the Design of Flavin Receptors. Issue 26 (11th May 2016)
- Record Type:
- Journal Article
- Title:
- Triazine‐Carbon Nanotubes: New Platforms for the Design of Flavin Receptors. Issue 26 (11th May 2016)
- Main Title:
- Triazine‐Carbon Nanotubes: New Platforms for the Design of Flavin Receptors
- Authors:
- Lucío, María Isabel
Pichler, Federica
Ramírez, José Ramón
de la Hoz, Antonio
Sánchez‐Migallón, Ana
Hadad, Caroline
Quintana, Mildred
Giulani, Angela
Bracamonte, Maria Victoria
Fierro, Jose L. G.
Tavagnacco, Claudio
Herrero, María Antonia
Prato, Maurizio
Vázquez, Ester - Abstract:
- 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. Abstract : Receptors on rods : Artificial receptors of flavins are synthesised by the functionalisation of carbon nanotubes with 1, 3, 5‐triazines (see figure). The ability of the nanotubes to recognise riboflavin is analysed by different techniques and the results highlight the major role of hydrogen bonds in the process. The possibility of modifying flavins and carbon nanotubes paves the way for the designAbstract: 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. Abstract : Receptors on rods : Artificial receptors of flavins are synthesised by the functionalisation of carbon nanotubes with 1, 3, 5‐triazines (see figure). The ability of the nanotubes to recognise riboflavin is analysed by different techniques and the results highlight the major role of hydrogen bonds in the process. The possibility of modifying flavins and carbon nanotubes paves the way for the design of specific receptors in catalytic processes. … (more)
- Is Part Of:
- Chemistry. Volume 22:Issue 26(2016)
- Journal:
- Chemistry
- Issue:
- Volume 22:Issue 26(2016)
- Issue Display:
- Volume 22, Issue 26 (2016)
- Year:
- 2016
- Volume:
- 22
- Issue:
- 26
- Issue Sort Value:
- 2016-0022-0026-0000
- Page Start:
- 8879
- Page End:
- 8888
- Publication Date:
- 2016-05-11
- Subjects:
- donor–acceptor systems -- molecular recognition -- nanotubes -- noncovalent interactions -- receptors
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.201600630 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1803.xml