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SERS/TERS Characterization of New Potential Therapeutics: The Influence of Positional Isomerism, Interface Type, Oxidation State of Copper, and Incubation Time on Adsorption on the Surface of Copper(I) and (II) Oxide Nanoparticles
[Image: see text] The aim of this study was to investigate how the oxidation state of copper (Cu(I) vs Cu(II)), the nature of the interface (solid/aqueous vs solid/air), positional isomerism, and incubation time affect the functionalization of the surface of copper oxide nanostructures by [(butylami...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8919263/ https://www.ncbi.nlm.nih.gov/pubmed/35230122 http://dx.doi.org/10.1021/acs.jmedchem.2c00031 |
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author | Proniewicz, Edyta Olszewski, Tomasz K. |
author_facet | Proniewicz, Edyta Olszewski, Tomasz K. |
author_sort | Proniewicz, Edyta |
collection | PubMed |
description | [Image: see text] The aim of this study was to investigate how the oxidation state of copper (Cu(I) vs Cu(II)), the nature of the interface (solid/aqueous vs solid/air), positional isomerism, and incubation time affect the functionalization of the surface of copper oxide nanostructures by [(butylamino)(pyridine)methyl]phenylphosphinic acid (PyPA). For this purpose, 2-, 3-, and 4-isomers of PyPA and the nanostructures were synthesized. The nanostructure were characterized by UV-visible spectroscopy (UV–vis), scanning electron microscopy (SEM), Raman spectroscopy (RS), and X-ray diffraction (XRD) analysis, which proved the formation of spherical Cu(2)O nanoparticles (Cu(2)ONPs; 1500–600 nm) and leaf-like CuO nanostructures (CuONSs; 80–180/400–700 nm, width/length). PyPA isomers were deposited on the surface of NSs, and adsorption was investigated by surface-enhanced Raman scattering (SERS) and tip-enhanced Raman scattering (TERS). The changes of adsorption on the surface of copper oxide NSs caused by the above-mentioned factors were described and the enhancement factor on this substrate was calculated. |
format | Online Article Text |
id | pubmed-8919263 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-89192632022-03-15 SERS/TERS Characterization of New Potential Therapeutics: The Influence of Positional Isomerism, Interface Type, Oxidation State of Copper, and Incubation Time on Adsorption on the Surface of Copper(I) and (II) Oxide Nanoparticles Proniewicz, Edyta Olszewski, Tomasz K. J Med Chem [Image: see text] The aim of this study was to investigate how the oxidation state of copper (Cu(I) vs Cu(II)), the nature of the interface (solid/aqueous vs solid/air), positional isomerism, and incubation time affect the functionalization of the surface of copper oxide nanostructures by [(butylamino)(pyridine)methyl]phenylphosphinic acid (PyPA). For this purpose, 2-, 3-, and 4-isomers of PyPA and the nanostructures were synthesized. The nanostructure were characterized by UV-visible spectroscopy (UV–vis), scanning electron microscopy (SEM), Raman spectroscopy (RS), and X-ray diffraction (XRD) analysis, which proved the formation of spherical Cu(2)O nanoparticles (Cu(2)ONPs; 1500–600 nm) and leaf-like CuO nanostructures (CuONSs; 80–180/400–700 nm, width/length). PyPA isomers were deposited on the surface of NSs, and adsorption was investigated by surface-enhanced Raman scattering (SERS) and tip-enhanced Raman scattering (TERS). The changes of adsorption on the surface of copper oxide NSs caused by the above-mentioned factors were described and the enhancement factor on this substrate was calculated. American Chemical Society 2022-03-01 2022-03-10 /pmc/articles/PMC8919263/ /pubmed/35230122 http://dx.doi.org/10.1021/acs.jmedchem.2c00031 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Proniewicz, Edyta Olszewski, Tomasz K. SERS/TERS Characterization of New Potential Therapeutics: The Influence of Positional Isomerism, Interface Type, Oxidation State of Copper, and Incubation Time on Adsorption on the Surface of Copper(I) and (II) Oxide Nanoparticles |
title | SERS/TERS Characterization
of New Potential Therapeutics:
The Influence of Positional Isomerism, Interface Type, Oxidation State
of Copper, and Incubation Time on Adsorption on the Surface of Copper(I)
and (II) Oxide Nanoparticles |
title_full | SERS/TERS Characterization
of New Potential Therapeutics:
The Influence of Positional Isomerism, Interface Type, Oxidation State
of Copper, and Incubation Time on Adsorption on the Surface of Copper(I)
and (II) Oxide Nanoparticles |
title_fullStr | SERS/TERS Characterization
of New Potential Therapeutics:
The Influence of Positional Isomerism, Interface Type, Oxidation State
of Copper, and Incubation Time on Adsorption on the Surface of Copper(I)
and (II) Oxide Nanoparticles |
title_full_unstemmed | SERS/TERS Characterization
of New Potential Therapeutics:
The Influence of Positional Isomerism, Interface Type, Oxidation State
of Copper, and Incubation Time on Adsorption on the Surface of Copper(I)
and (II) Oxide Nanoparticles |
title_short | SERS/TERS Characterization
of New Potential Therapeutics:
The Influence of Positional Isomerism, Interface Type, Oxidation State
of Copper, and Incubation Time on Adsorption on the Surface of Copper(I)
and (II) Oxide Nanoparticles |
title_sort | sers/ters characterization
of new potential therapeutics:
the influence of positional isomerism, interface type, oxidation state
of copper, and incubation time on adsorption on the surface of copper(i)
and (ii) oxide nanoparticles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8919263/ https://www.ncbi.nlm.nih.gov/pubmed/35230122 http://dx.doi.org/10.1021/acs.jmedchem.2c00031 |
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