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RDF description of Triazine-Carbon Nanotubes: New Platforms for the Design of Flavin Receptors - http://orbis.uaslp.mx/vivo/individual/scopus4712
rights: termsOfUse
date: 2026-08-24T04:43:32
publisher: vivo
type: Document

European Regional Development Fund, FEDER: PEII-2014-002A
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funding vehicle for: Triazine-Carbon Nanotubes: New Platforms for the Design of Flavin Receptors

Article
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2010N3T9M4
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funding vehicle for: Triazine-Carbon Nanotubes: New Platforms for the Design of Flavin Receptors

Document
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Triazine-Carbon Nanotubes: New Platforms for the Design of Flavin Receptors
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has funding vehicle: European Regional Development Fund, FEDER: PEII-2014-002A
related by: authorship_27671
type: Article
chemicalscas: riboflavin, 83-88-5; Nanotubes, Carbon; Riboflavin; Triazines
related by: authorship_27661
related by: authorship_27666
type: Information Content Entity
related by: authorship_27672
related by: authorship_27667
has funding vehicle: 2010N3T9M4
issue: 26
related by: authorship_27670
crisid: 4713
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date time value: article date 4713
related by: authorship_27664
estado: published
most specific type: Article
type: Generically Dependent Continuant
related by: authorship_27665
volume: 22
origen: scopus
has funding vehicle: Universidad de Castilla-La Mancha, UCLM
page end: 8888
has funding vehicle: Ministerio de Economía y Competitividad, MINECO: CTQ2011-22410, CTQ2014-53600-R
freetext keyword: donor–acceptor systems; molecular recognition; nanotubes; noncovalent interactions; receptors Hydrogen bonds; Ions; Microwave irradiation; Molecular recognition; Nanotubes; Single-walled carbon nanotubes (SWCN); Artificial receptors; Association constant; Control of the interaction; Functionalised carbon nanotubes; Non-covalent interaction; receptors; Spectroscopic technique; Triazine derivatives; Multiwalled carbon nanotubes (MWCN); carbon nanotube; riboflavin; triazine derivative; catalysis; chemistry; hydrogen bond; microwave radiation; spectrofluorometry; thermogravimetry; transmission electron microscopy; ultraviolet spectrophotometry; X ray photoelectron spectroscopy; Catalysis; Hydrogen Bonding; Microscopy, Electron, Transmission; Microwaves; Nanotubes, Carbon; Photoelectron Spectroscopy; Riboflavin; Spectrometry, Fluorescence; Spectrophotometry, Ultraviolet; Thermogravimetry; Triazines
e iscopus: 2-s2.0-84966508481
doi: 10.1002/chem.201600630
related by: authorship_27669
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. © 2016 WILEY-VCH Verlag GmbH %26 Co. KGaA, Weinheim
page start: 8879
type: Continuant
related by: authorship_27662
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. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
related by: authorship_27663
related by: authorship_27660
type: Document
has publication venue: Chemistry - A European Journal
related by: authorship_27668
pmid: 27168484
related by: authorship_27673

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Universidad de Castilla-La Mancha, UCLM
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type: BFO_0000020
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funding vehicle for: Triazine-Carbon Nanotubes: New Platforms for the Design of Flavin Receptors

Ministerio de Economía y Competitividad, MINECO: CTQ2011-22410, CTQ2014-53600-R
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type: BFO_0000020
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funding vehicle for: Triazine-Carbon Nanotubes: New Platforms for the Design of Flavin Receptors

Chemistry - A European Journal
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publication venue for: Triazine-Carbon Nanotubes: New Platforms for the Design of Flavin Receptors
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Information Content Entity
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