Cargando…

Hybrid Sol–Gel Matrices Doped with Colorimetric/Fluorimetric Imidazole Derivatives †

Organic–inorganic hybrids (OIH) are materials that can be easily synthesized by the sol–gel method and combine the advantages of organic and inorganic moieties within a single polymeric matrix. Imidazole derivatives are versatile organic compounds that can change their optical properties with the va...

Descripción completa

Detalles Bibliográficos
Autores principales: Sousa, Rui P. C. L., Figueira, Rita B., Gomes, Bárbara R., Sousa, Sara, Ferreira, R. Cristina M., Costa, Susana P. G., Raposo, M. Manuela M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8705321/
https://www.ncbi.nlm.nih.gov/pubmed/34947750
http://dx.doi.org/10.3390/nano11123401
_version_ 1784621917280403456
author Sousa, Rui P. C. L.
Figueira, Rita B.
Gomes, Bárbara R.
Sousa, Sara
Ferreira, R. Cristina M.
Costa, Susana P. G.
Raposo, M. Manuela M.
author_facet Sousa, Rui P. C. L.
Figueira, Rita B.
Gomes, Bárbara R.
Sousa, Sara
Ferreira, R. Cristina M.
Costa, Susana P. G.
Raposo, M. Manuela M.
author_sort Sousa, Rui P. C. L.
collection PubMed
description Organic–inorganic hybrids (OIH) are materials that can be easily synthesized by the sol–gel method and combine the advantages of organic and inorganic moieties within a single polymeric matrix. Imidazole derivatives are versatile organic compounds that can change their optical properties with the variation of pH due to the protonation or deprotonation of the nitrogen atoms. This work reports the preparation of different OIHs doped with different contents of two imidazole compounds (3a,b). The obtained materials were characterized structurally by FTIR, and the dielectric properties were studied by electrochemical impedance spectroscopy. The optical properties were studied by UV-Vis absorption and fluorescence spectroscopies. The FTIR analysis showed that the presence of the imidazole does not change the structural properties of the matrices. The normalized resistance values obtained for the doped matrices ranged between 8.57 and 9.32 Ω cm(2), all being higher than the undoped matrix. The σ ranged between 9.49 and 10.28 S cm(−1), being all higher than the pure OIH samples. Compound 3a showed a maximum absorption peak at 390 nm, which is present in the OIH spectra, proving the presence of the compound. In the case of compound 3b, a maximum absorption wavelength at 412 nm was found, and the compound peak was not clear, which may indicate that an interaction between the compound and the matrix occurred. A synergetic effect between the intrinsic emission of the matrix and the fluorescence of 3a is found on the OIH-doped matrices.
format Online
Article
Text
id pubmed-8705321
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-87053212021-12-25 Hybrid Sol–Gel Matrices Doped with Colorimetric/Fluorimetric Imidazole Derivatives † Sousa, Rui P. C. L. Figueira, Rita B. Gomes, Bárbara R. Sousa, Sara Ferreira, R. Cristina M. Costa, Susana P. G. Raposo, M. Manuela M. Nanomaterials (Basel) Article Organic–inorganic hybrids (OIH) are materials that can be easily synthesized by the sol–gel method and combine the advantages of organic and inorganic moieties within a single polymeric matrix. Imidazole derivatives are versatile organic compounds that can change their optical properties with the variation of pH due to the protonation or deprotonation of the nitrogen atoms. This work reports the preparation of different OIHs doped with different contents of two imidazole compounds (3a,b). The obtained materials were characterized structurally by FTIR, and the dielectric properties were studied by electrochemical impedance spectroscopy. The optical properties were studied by UV-Vis absorption and fluorescence spectroscopies. The FTIR analysis showed that the presence of the imidazole does not change the structural properties of the matrices. The normalized resistance values obtained for the doped matrices ranged between 8.57 and 9.32 Ω cm(2), all being higher than the undoped matrix. The σ ranged between 9.49 and 10.28 S cm(−1), being all higher than the pure OIH samples. Compound 3a showed a maximum absorption peak at 390 nm, which is present in the OIH spectra, proving the presence of the compound. In the case of compound 3b, a maximum absorption wavelength at 412 nm was found, and the compound peak was not clear, which may indicate that an interaction between the compound and the matrix occurred. A synergetic effect between the intrinsic emission of the matrix and the fluorescence of 3a is found on the OIH-doped matrices. MDPI 2021-12-15 /pmc/articles/PMC8705321/ /pubmed/34947750 http://dx.doi.org/10.3390/nano11123401 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sousa, Rui P. C. L.
Figueira, Rita B.
Gomes, Bárbara R.
Sousa, Sara
Ferreira, R. Cristina M.
Costa, Susana P. G.
Raposo, M. Manuela M.
Hybrid Sol–Gel Matrices Doped with Colorimetric/Fluorimetric Imidazole Derivatives †
title Hybrid Sol–Gel Matrices Doped with Colorimetric/Fluorimetric Imidazole Derivatives †
title_full Hybrid Sol–Gel Matrices Doped with Colorimetric/Fluorimetric Imidazole Derivatives †
title_fullStr Hybrid Sol–Gel Matrices Doped with Colorimetric/Fluorimetric Imidazole Derivatives †
title_full_unstemmed Hybrid Sol–Gel Matrices Doped with Colorimetric/Fluorimetric Imidazole Derivatives †
title_short Hybrid Sol–Gel Matrices Doped with Colorimetric/Fluorimetric Imidazole Derivatives †
title_sort hybrid sol–gel matrices doped with colorimetric/fluorimetric imidazole derivatives †
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8705321/
https://www.ncbi.nlm.nih.gov/pubmed/34947750
http://dx.doi.org/10.3390/nano11123401
work_keys_str_mv AT sousaruipcl hybridsolgelmatricesdopedwithcolorimetricfluorimetricimidazolederivatives
AT figueiraritab hybridsolgelmatricesdopedwithcolorimetricfluorimetricimidazolederivatives
AT gomesbarbarar hybridsolgelmatricesdopedwithcolorimetricfluorimetricimidazolederivatives
AT sousasara hybridsolgelmatricesdopedwithcolorimetricfluorimetricimidazolederivatives
AT ferreirarcristinam hybridsolgelmatricesdopedwithcolorimetricfluorimetricimidazolederivatives
AT costasusanapg hybridsolgelmatricesdopedwithcolorimetricfluorimetricimidazolederivatives
AT raposommanuelam hybridsolgelmatricesdopedwithcolorimetricfluorimetricimidazolederivatives