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- Detection of azo dyes using carbon dots from olive mill wastesPublication . Sousa, Diogo A.; Berberan-Santos, Mario; Prata, José VirgílioAzo dyes are widely spread in our day life, being heavily used in cosmetics, healthcare products, textile industries, and as artificial food colorants. This intense industrial activity, which inherently includes their own production, inexorably leads to uncontrolled release of dyes into the environment. As emerging pollutants, their detection, particularly in water systems, is a priority. Herein, a fluorescence-based method was employed for the sensitive and selective detection of anionic and neutral azo dyes. Carbon dots (CDs) synthesized from wet pomace (WP), an abundant semi-solid waste of olive mills, were used as probes. An outstanding capability for detection of azo dyes methyl orange (MO) and methyl red (MR) in aqueous solutions was disclosed, which reached a limit of detection (LOD) of 151 ppb for MO. The selectivity of WP-CDs for the anionic azo dye (MO) was established through competitive experiments with other dyes, either anionic (indigo carmine) or cationic (fuchsin, methylene blue, and rhodamine 6G); perchlorate salts of transition metal cations (Cu(II), Co(II), Fe(II), Fe(III), Hg(II), and Pb(II)); and sodium salts of common anions (NO3-, CO32-, Cl-, and SO42-). Evidence has been collected that supports static quenching as the main transduction event underlying the observed quenching of the probe's fluorescence, combined with a dynamic resonance energy transfer (RET) mechanism at high MO concentrations.
- Carbon dots from coffee grounds by a one-pot microwave-assisted methodPublication . Moraes, Bianca; Costa, Alexandra I.; Barata, Patrícia; Prata, José V.Carbon-based nanomaterials, particularly carbon dots (C-dots) have attracted the researchers interest due their excellent luminescence, photostability and biocompatibility, encouraging their use in several areas such as biomedicine, (bio)sensors, photocatalysis and optoelectronics. C-dots could be prepared by a variety of methods (top-down and bottom-up approaches), using a great diversity of carbon sources. Bottom-up processes based on the use of waste materials for producing C-dots are particularly attractive since an effective reduction of environmental impacts of those wastes may be foreseen, while high-valued nanomaterials can be simultaneously obtained. Coffee is one of the most consumed brews all over the world, generating large amounts of coffee waste, a source of a serious environmental problem due to the high content of organic matter such as caffeine, phenols, tannins, and sugars. Herein, we explore the valorization of coffee grounds generated from automatic and vending machines for production of C-dots through a one-pot monomode microwave-assisted method. Structural and photophysical characterization of the as-synthesized nanomaterials have been carried out, and their potential applications as sensing materials for pollutants and explosives (e.g. nitroanilines and nitroaromatics) were evaluated by fluorescence and absorption techniques.
- A solid-state fluorescence sensor for nitroaromatics and nitroanilines based on a conjugated Calix[4]arene polymerPublication . Prata, José V.; Costa, Alexandra I.; Teixeira, CarlosA new conjugated polymer possessing calix[4]arene-oxacyclophane units wired-in-series by phenyleneethynylene linkers was synthesized by a Sonogashira-Hagihara cross-coupling method in high yield. The polymer was structurally characterized by FTIR and 1H/13C/HSQC NMR techniques, and its average Mn (38.5 kDa) retrieved from GPC analysis. The polymer is highly emissive (ΦF =0.55) and exhibits a longer-than-usual excited-state lifetime (1.80 ns) for a phenyleneethynylene type polymer. Similar photo physical properties (absorption and fluorescence emission) were observed in solution and insolid-state. This stems from the presence of bulky calixarene moieties along the polymer chains which prevent interchain staking and the formation of ground-state aggregates and/or non-emissive exciplexes, both deleterious to solid-state materials envisioned for fluorescence sensing applications. Moreover, the intrinsic molecular recognition capabilities of its two rigid inner cavities (calixarene and cyclophane sub-units), allied with the high three-dimensionality of the macromolecule that creates additional interstitial voids around the molecular receptors, can boost its sensory responses towards specific analytes. A high sensitive response was observed in the detection of nitroaromatics and nitroanilines in neat vapour phases by casted films of the polymer. The largest sensitivitieswereobtainedfor2,4-dinitrotoluene (a taggant for the explosive TNT;>85% of fluorescence quenching upon 1 min exposure) and ortho-nitroaniline (90% of emission reduction in 30s).The sensory responses attained in solid-state are discussed on the basis of the electron affinities of the analytes and their electrostatic interactions with polymer films.
- Finding value in wastewaters from the cork industry: carbon dots synthesis and fluorescence for hemeprotein detectionPublication . Alexandre, Marta R.; Costa, Alexandra I.; Berberan-Santos, Mario; Prata, José V.Valorisation of industrial low-value waste residues was preconized. Hence, carbon dots (C-dots) were synthesized from wastewaters of the cork industry—an abundant and a_ordable, but environmentally-problematic industrial e_uent. The carbon nanomaterials were structurally and morphologically characterised, and their photophysical properties were analysed by an ensemble of spectroscopy techniques. Afterwards, they were successfully applied as highly-sensitive fluorescence probes for the direct detection of haemproteins. Haemoglobin, cytochrome c and myoglobin were selected as specific targets owing to their relevant roles in living organisms, wherein their deficiencies or surpluses are associated with several medical conditions. For all of them, remarkable responses were achieved, allowing their detection at nanomolar levels. Steady-state and time-resolved fluorescence, ground-state UV–Vis absorption and electronic circular dichroism techniques were used to investigate the probable mechanisms behind the fluorescence turn-o_ of C-dots. Extensive experimental evidence points to a static quenching mechanism. Likewise, resonance energy transfer and collisional quenching have been discarded as excited-state deactivating mechanisms. It was additionally found that na oxidative, photoinduced electron transfer occurs for cytochrome c, the most electron-deficient protein Besides, C-dots prepared from citric acid/ethylenediamine were comparatively assayed for protein detection and the di_erences between the two types of nanomaterials highlighted.
- 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).
- Novel C-dots/titanate nanotubular hybrid materials with enhanced optical and photocatalytic propertiesPublication . Alves, D. M.; Prata, José Virgílio; Silvestre, António Jorge; Monteiro, O. C.Advanced nanomaterials with enhanced optical and photocatalytic properties for the photodegradation of organic pollutants, in particular pharmaceuticals and personal care products (PPCPs), were successfully prepared by a swift one-pot synthesis. Nanostructured materials were synthesized through an integrated hydrothermal procedure which generates titanate nanotubes (TNTs) with different carbon dots (C-dots) contents, from an amorphous titanium oxide-based source and cork industry wastewaters (CIWW) as carbon source. Their structural, microstructural, morphological, and optical properties were studied by XRD, TEM, XPS, UV-Vis diffuse reflectance and photoluminescence spectroscopies. As aimed, the hybrid C-dots/ TNT nanomaterials extend their light absorption towards the red, in comparison to pristine TNT, prompting them for a more efficient use of light in photocatalysis by widening the TNT energy uptake range. The decrease of bandgap energy with increasing sample's C-dots content seems to be originated from energy intermediate states formed within the TNTs' forbidden band resulting from Ti-O-C bonds established between the TNTs and the C-dots that form tails of states.The as-synthesized C-dots/TNT samples were tested in the photodegradation of caffeine as a pollutant model for PPCPs. Rewarding results were obtained, with the hybrid C-dots/TNT nanomaterials showing significant enhanced photocatalytic ability toward caffeine degradation in comparison to pristine TNTs. Photocatalysis assays in the presence of scavengers and/or in the absence of oxygen were also performed aiming to characterize the most reactive species formed during the semiconductor photo-activation process and thus assessing to possible reactive pathways underpinning the photocatalytic activity of the hybrid C-dots/TNT nanomaterials.
- Highly sensitive and selective fluorescent probes for Cu(II) detection based on calix[4]arene-oxacyclophane architecturesPublication . Costa, Alexandra I.; Barata, Patrícia; Fialho, Carina; Prata, José V.A new topological design of fluorescent probes for sensing copper ion is disclosed. The calix[4]arene-oxacyclophane (Calix-OCP) receptor, either wired-in-series in arylene-alt-ethynylene conjugated polymers or standing alone as a sole molecular probe, display a remarkable a_nity and selectivity for Cu(II). The unique recognition properties of Calix-OCP system toward copper cation stem from its pre-organised cyclic array of O-ligands at the calixarene narrow rim, which is kept in a conformational rigid arrangement by a tethered oxacyclophane sub-unit. The magnitude of the binding constants (Ka = 5.30 8.52 _ 104 M1) and the free energy changes for the inclusion complexation (DG = 27.0 28.1 kJmol1), retrieved from fluorimetric titration experiments, revealed a high sensitivity of Calix-OCP architectures for Cu(II) species. Formation of supramolecular inclusion complexes was evidenced from UV-Vis spectroscopy. The new Calix-OCP-conjugated polymers (polymers 4 and 5), synthesized in good yields by Sonogashira–Hagihara methodologies, exhibit high fluorescence quantum yields (_F = 0.59 0.65). Density functional theory (DFT) calculations were used to support the experimental findings. The fluorescence on–o_ behaviour of the sensing systems is tentatively explained by a photoinduced electron transfer mechanism.
- Fluorescent calix[4]arene-carbazole-containing polymers as sensors for nitroaromatic explosivesPublication . Barata, Patrícia; Prata, José VirgílioTwo highly fluorescent calix[4]arene-containing phenylene-alt-ethynylene-carbazolylene polymers (Calix-PPE-CBZs) were used in the detection of explosives from the nitroaromatic compounds (NACs) family, in solution and in vapour phases. Both fluorophores exhibit high sensitivity and selectivity towards NACs detection. The quenching efficiencies in solution, assessed through static Stern-Volmer constants (K-SV), follow the order picric acid (PA) >> 2,4,6-trinitrotoluene (TNT) > 2,4-dinitrotoluene > (2,4-DNT) > nitrobenzene (NB). These correlate very well with the NACs electron affinities, as evaluated from their lowest unoccupied molecular orbitals (LUMOs) energies, indicating a photo-induced electron transfer as the dominant mechanism in fluorescence quenching. Moreover, and most interesting, detection of TNT, 2,4-DNT and NB vapours via thin-films of Calix-PPE-CBZs revealed a remarkably sensitive response to these analytes, comparable to state-of-the-art chemosensors. The study also analyses and compares the current results to previous disclosed data on the detection of NACs by several calix[4]arene-based conjugated polymers and non-polymeric calix[4]arenes-carbazole conjugates, overall highlighting the superior role of calixarene and carbazole structural motifs in NACs' detection performance. Density functional theory (DFT) calculations performed on polymer models were used to support some of the experimental findings.