Loading...
3 results
Search Results
Now showing 1 - 3 of 3
- Carbon dots synthesis from coffee grounds, and sensing of nitroanilinesPublication . Moraes, Bianca; Costa, Alexandra I.; Barata, Patrícia; Prata, José V.Fluorescent carbon dots (C-dots) were directly synthesized by a sustainable and eco friendly one-pot microwave-assisted hydrothermal carbonization method from coffee grounds waste. The coffee grounds obtained from automatic coffee machines, after being heated at 190 °C for 1–4 h in the presence of nitrogen additives, furnished the desired carbon nanomaterials. Struc tural and photophysical properties of the as-synthesized nanomaterials were evaluated by FTIR, 1H NMR, UV-Vis, and fluorescence spectroscopies. The ability of the C-dots to behave as probes for isomeric nitroanilines (ortho-, meta- and para-nitroaniline) was explored through fluorimetric titra tion experiments. High sensitivities and selectivities were obtained for the detection of nitroanilines in aqueous media.
- Carbon dots from coffee grounds: synthesis, characterization, and detection of noxious nitroanilinesPublication . Costa, Alexandra I.; Barata, Patrícia; Moraes, Bianca; Prata, José V.Coffee ground (CG) waste is generated in huge amounts all over the world, constituting a serious environmental issue owing to its low biodegradability. Therefore, processes that simultaneously aim for its valorization while reducing its environmental impact are in great demand. In the current approach, blue luminescent carbon dots (C-dots) were produced in good chemical yields from CGs following hydrothermal carbonization methods under an extended set of reaction parameters. The remarkable fluorescent properties of the synthesized C-dots (quantum yields up to 0.18) allied to their excellent water dispersibility and photostability prompted their use for the first time as sensing elements for detection of noxious nitroanilines (NAs) in aqueous media. Very high levels of NA detection were achieved (e.g., limit of detection of 68 ppb for p-nitroaniline), being the regioisomeric selectivity attributed to its higher hyperpolarizability and dipole moment. Through ground-state and time-resolved fluorescence assays, a static fluorescence quenching mechanism was established. H-1 NMR titration data also strongly suggested the formation of ground-state complexes between C-dots and NAs.
- Fluorescent bis-calix[4]arene-carbazole conjugates: synthesis and inclusion complexation studies with fullerenes C-60 and C-70Publication . Barata, Patrícia; Costa, Alexandra I.; Costa, Sérgio; Prata, José V.Supramolecular chemistry has become a central theme in chemical and biological sciences over the last decades. Supramolecular structures are being increasingly used in biomedical applications, particularly in devices requiring specific stimuli-responsiveness. Fullerenes, and supramolecular assemblies thereof, have gained great visibility in biomedical sciences and engineering. Sensitive and selective methods are required for the study of their inclusion in complexes in various application fields. With this in mind, two new fluorescent bis-calix[4]arene-carbazole conjugates (4 and 5) have been designed. Herein, their synthesis and ability to behave as specific hosts for fullerenes C-60 and C-70 is described. The optical properties of the novel compounds and their complexes with C-60 and C-70 were thoroughly studied by UV-Vis and steady-state and time-resolved fluorescence spectroscopies. The association constants (K-a) for the complexation of C-60 and C-70 by 4 and 5 were determined by fluorescence techniques. A higher stability was found for the C-70@4 supramolecule (K-a = 5.6 x 10(4) M-1; Delta G = -6.48 kcal/mol). Evidence for the formation of true inclusion complexes between the host 4 and C-60/C-70 was obtained from NMR spectroscopy performed at low temperatures. The experimental findings were fully corroborated by density functional theory (DFT) models performed on the host-guest assemblies (C-60@4 and C-70@4).