Poly-2-aminomethyl-3-(3,4-dihydroxyphenyl)propionamide: From Structure to Proprieties AITranslate
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The oxidative polymerization of the dopamine analogue, 2-aminomethyl-3-(3,4-dihydroxyphenyl)propionamide (DL), is presented and its polymerization product, PDL, is fully characterized both in bulk and as a coating layer on TiO2 and glass substrates. Standard oxidation conditions in 10 mM TrisCl aqueous solution at pH = 8.5 were employed for directly referencing the PDL characteristic features to those of polydopamine. These features were investigated by scanning electron microscopy (SEM)/transmission electron microscopy (TEM), atomic force microscopy (AFM), DSC/TGA, MS-ESI(+), Zeta, ss-NMR, EPR, X-ray photoelectron spectroscopy (XPS), Fourier-transform infrared (FT-IR), and ultraviolet–visible (UV–vis). Selective 13C and 15N isotopic labelling of the key chemical position in the DL side chain has facilitated the ss-NMR structural characterization of PDL and a better understanding of its polymerization mechanism. PDL shows fluorescence with a maximum 4% quantum yield when dissolved in methanol and better antibacterial effect compared to PDA, especially against Staphylococcus aureus.
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DOI:https://doi.org/10.1021/acsapm.3c00027
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The oxidative polymerization of the dopamine analogue, 2-aminomethyl-3-(3,4-dihydroxyphenyl)propionamide (DL), is presented and its polymerization product, PDL, is fully characterized both in bulk and as a coating layer on TiO2 and glass substrates. Standard oxidation conditions in 10 mM TrisCl aqueous solution at pH = 8.5 were employed for directly referencing the PDL characteristic features to those of polydopamine. These features were investigated by scanning electron microscopy (SEM)/transmission electron microscopy (TEM), atomic force microscopy (AFM), DSC/TGA, MS-ESI(+), Zeta, ss-NMR, EPR, X-ray photoelectron spectroscopy (XPS), Fourier-transform infrared (FT-IR), and ultraviolet–visible (UV–vis). Selective 13C and 15N isotopic labelling of the key chemical position in the DL side chain has facilitated the ss-NMR structural characterization of PDL and a better understanding of its polymerization mechanism. PDL shows fluorescence with a maximum 4% quantum yield when dissolved in methanol and better antibacterial effect compared to PDA, especially against Staphylococcus aureus.
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| GB/T 7714-2015 | [1] Anca Petran, Andreea Petronela Crişan, Claudia Lar, et al. ACS Applied Polymer Materials, 2023(5). DOI:10.1021/acsapm.3c00027. |
| MLA | [1] Anca Petran, et al., ACS Applied Polymer Materials, no. 5, 2023, https://doi.org/10.1021/acsapm.3c00027. |
| APA | [1] Anca Petran, Andreea Petronela Crişan, Claudia Lar, Adriana Popa, Teodora Radu, Alexandra Cioriţă, Diana Bogdan, Mihaela Silion, & Claudiu Filip. (2023). ACS Applied Polymer Materials(5). https://doi.org/10.1021/acsapm.3c00027 |
| IEEE | [1] Anca Petran, Andreea Petronela Crişan, Claudia Lar, Adriana Popa, Teodora Radu, Alexandra Cioriţă, Diana Bogdan, Mihaela Silion, and Claudiu Filip, ACS Applied Polymer Materials, no. 5, 2023, doi: 10.1021/acsapm.3c00027. keywords: {polydopamine analogues;isotopic labeling;fluorescence;surface coating;biomedical applications} |
