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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2019
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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. |
format | Online Article Text |
id | pubmed-6648563 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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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