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Phe–Phe Di-Peptide Nanostructure Self-Assembling Modulated by Luminescent Additives

[Image: see text] In this work, supramolecular l-l-diphenylalanine (Phe–Phe) nanostructures were self-assembled in solvents of distinct polarity and in the presence of luminescent additives of distinct conjugation length that physically adhere to the nanostructures to provide growth environments of...

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Autores principales: Ribeiro, Antonio C. C., Souza, Geovany A., Pereira, Douglas Henrique, Cordeiro, Diericon S., Miranda, Ramon S., Custódio, Rogério, Martins, Tatiana D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648563/
https://www.ncbi.nlm.nih.gov/pubmed/31459351
http://dx.doi.org/10.1021/acsomega.8b02732
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author Ribeiro, Antonio C. C.
Souza, Geovany A.
Pereira, Douglas Henrique
Cordeiro, Diericon S.
Miranda, Ramon S.
Custódio, Rogério
Martins, Tatiana D.
author_facet Ribeiro, Antonio C. C.
Souza, Geovany A.
Pereira, Douglas Henrique
Cordeiro, Diericon S.
Miranda, Ramon S.
Custódio, Rogério
Martins, Tatiana D.
author_sort Ribeiro, Antonio C. C.
collection PubMed
description [Image: see text] In this work, supramolecular l-l-diphenylalanine (Phe–Phe) nanostructures were self-assembled in solvents of distinct polarity and in the presence of luminescent additives of distinct conjugation length that physically adhere to the nanostructures to provide growth environments of distinct properties. When the additive is poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene], an electron donor polymer, and solvent is tetrahydrofuran (THF), Phe–Phe vesicle-like structures are obtained, whereas in water and in the presence of a similar additive in structure, poly[5-methoxy-2-(3-sulfopropoxy)-1,4-phenylenevinylene], nanotubes are formed. In contrast, when 9-vinyl-carbazole, an electron acceptor additive is used, nanotubes are formed even when THF is the solvent. The same structures are obtained when the additive is the macromolecule poly(vinyl carbazole). The morphologies of these self-assembled structures were observed by scanning electron microscopy, and their photophysical behavior was determined by steady-state fluorescence spectroscopy and time-resolved fluorescence spectroscopy. These data analyzed altogether inform about the formation mechanisms of such structures and about the influence that distinct interactions exert on self-assembling and charge-transfer processes through formation of complexes between the luminescent additives and the Phe–Phe nano- and microstructures.
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spelling pubmed-66485632019-08-27 Phe–Phe Di-Peptide Nanostructure Self-Assembling Modulated by Luminescent Additives Ribeiro, Antonio C. C. Souza, Geovany A. Pereira, Douglas Henrique Cordeiro, Diericon S. Miranda, Ramon S. Custódio, Rogério Martins, Tatiana D. ACS Omega [Image: see text] In this work, supramolecular l-l-diphenylalanine (Phe–Phe) nanostructures were self-assembled in solvents of distinct polarity and in the presence of luminescent additives of distinct conjugation length that physically adhere to the nanostructures to provide growth environments of distinct properties. When the additive is poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene], an electron donor polymer, and solvent is tetrahydrofuran (THF), Phe–Phe vesicle-like structures are obtained, whereas in water and in the presence of a similar additive in structure, poly[5-methoxy-2-(3-sulfopropoxy)-1,4-phenylenevinylene], nanotubes are formed. In contrast, when 9-vinyl-carbazole, an electron acceptor additive is used, nanotubes are formed even when THF is the solvent. The same structures are obtained when the additive is the macromolecule poly(vinyl carbazole). The morphologies of these self-assembled structures were observed by scanning electron microscopy, and their photophysical behavior was determined by steady-state fluorescence spectroscopy and time-resolved fluorescence spectroscopy. These data analyzed altogether inform about the formation mechanisms of such structures and about the influence that distinct interactions exert on self-assembling and charge-transfer processes through formation of complexes between the luminescent additives and the Phe–Phe nano- and microstructures. American Chemical Society 2019-01-09 /pmc/articles/PMC6648563/ /pubmed/31459351 http://dx.doi.org/10.1021/acsomega.8b02732 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Ribeiro, Antonio C. C.
Souza, Geovany A.
Pereira, Douglas Henrique
Cordeiro, Diericon S.
Miranda, Ramon S.
Custódio, Rogério
Martins, Tatiana D.
Phe–Phe Di-Peptide Nanostructure Self-Assembling Modulated by Luminescent Additives
title Phe–Phe Di-Peptide Nanostructure Self-Assembling Modulated by Luminescent Additives
title_full Phe–Phe Di-Peptide Nanostructure Self-Assembling Modulated by Luminescent Additives
title_fullStr Phe–Phe Di-Peptide Nanostructure Self-Assembling Modulated by Luminescent Additives
title_full_unstemmed Phe–Phe Di-Peptide Nanostructure Self-Assembling Modulated by Luminescent Additives
title_short Phe–Phe Di-Peptide Nanostructure Self-Assembling Modulated by Luminescent Additives
title_sort phe–phe di-peptide nanostructure self-assembling modulated by luminescent additives
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648563/
https://www.ncbi.nlm.nih.gov/pubmed/31459351
http://dx.doi.org/10.1021/acsomega.8b02732
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