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- 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.
- Polímeros fluorescentes para a detecção de metais tóxicosPublication . Fialho, Carina B.; Barata, Patrícia; Prata, José V.; Costa, Alexandra I.As reconhecidas capacidades dos calixarenos como receptores moleculares sintéticos, capazes de interagir e formar, selectivamente, complexos com espécies moleculares e iónicas, suscitaram o nosso interesse na sua incorporação em sistemas poliméricos conjugados, perspectivando a ocorrência da amplificação do sinal de transdução em processos de detecção de explosivos [1] e biomoléculas [2]. Na presente comunicação será apresentada a síntese, caracterização e aplicação sensorial a metais tóxicos de polímeros baseados em unidades de calix[4]arenos ditópicos e dietinil-9-propil-9H-carbazoles (CALIX-OCF-PPE-2,7-CBZeCALIX-OCF-PPE-3,6-CBZ).
- Metal ion recognition induced by calix[4]arene carbazole containing polymersPublication . D. Barata, Patrícia; Costa, Alexandra; Fialho, Carina B.; Prata, José VirgílioSensing and recognition of ions and neutral molecules via synthetic receptors are of current interest in supramolecular chemistry because of their significant importance in several areas, such as chemistry, biology and environment. Compared with small molecules, polymers-based sensors displayed several importante advantages like signal amplification. In this way, the incorporation of molecular receptors such as calixarenes with conjugated polymer backbones is expected to enhance the signaling events related to a host–guest interaction. The preorganized binding sites, easy derivatization and flexible three-dimensional steric structures make calixarenes ideal construction platforms for molecular design to generate fluorescente receptors. The use of calixarenes as supramolecular scaffolds for this type of architectures has been explored and the sensing abilities of resultant polymers toward metal and molecular ions established. Based on the high sensitivity shown by the non-polymeric analogue CALIX-OCP-CBZ (notshown), to toxic metal cations, we decide two extend the sensing study to polymer materials. Herein, we report the preliminar results of the chemosensing ability of a new bicyclic calix[4]arene-carbazole-polymer (CALIX-OCP-PPE-CBZ) towards the detection of toxic metals in fluid phase.
- Linear and crosslinked copolymers of p-tert-butylcalix[4]arene derivatives and styrene: new synthetic approaches to polymer-bound calix[4]arenesPublication . Mendes, Ana R.; Gregório, Carla C.; Barata, Patrícia; Costa, Alexandra I.; Prata, José V.As an extension of our previous studies concerning the free radical copolymerisation of 25,26,27-tripropoxy-28-(4-vinyl-benzyloxy)-p-tert-butylcalix[4]arene (3) with styrylic monomers, we report herein on the synthesis and characterisation of new terpolymers derived from 3, styrene and divinylbenzene, having nominal crosslinking degrees ranging from 4% to 40% wt. The terpolymers exhibited good thermal stabilities (DSC) and were prepared in good yields. Depending on the reaction conditions (dilution degree and aqueous phase to porogen ratio), materials with identical nominal crosslinking but otherwise differentiated morphologies and swelling abilities were obtained. In a related study, the radical polymerisation of styrene was carried out in the presence of a novel calix[4]arene derivative 4, bearing two distal benzyl–vinyl groups in the lower rim. It is shown that, albeit the presence of two phenolic groups within the calixarene moiety which could have functioned as inhibitors of the free radical polymerisation, the macrocycle was able to take part in the copolymerisation reaction, yielding new soluble and crosslinked polymers. In both cases, no pendant vinyl groups were found in the polymeric materials. The probable mechanisms underlying their formation are discussed.
- Fostering protein-calixarene interactions: from molecular recognition to sensingPublication . Prata, José Virgílio; D. Barata, PatríciaTwo isomeric bis-calixarene-carbazole conjugates (CCC-1 and CCC-2) endowed with carboxylic acid functions at their lower rims have been found to display a high sensing ability (KSV up to 6 x 10(7) M-1) and selectivity toward cytochrome c, a multi-functional protein, in an aqueous-based medium. After targeting basic amino acid residues on the protein surface residing near the prosthetic heme group through electrostatic and hydrophobic interactions, a rapid photoinduced electron transfer ensues between the integrated transduction element (aryleneethynylene chromophore) of CCCs and the iron-oxidized heme of cytochrome c, enabling direct detection of the protein at nanomolar levels. Our results show that CCCs are capable of efficiently discriminating heme proteins (cytochrome c vs. myoglobin) and non-heme proteins (lysozyme) in an aqueous medium. Studies performed in two solvent systems (organic and aqueous) strongly suggest that in an organic medium a Forster-type resonance energy transfer is responsible for the observed reduction in CCCs emission upon contact with heme proteins while in an aqueous medium a specific photoinduced electron transfer mechanism prevails.
- 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.
- Adsorption of myoglobin on calixarenes and biocatalysis in organic mediaPublication . Semedo, Magda C.; Karmali, Amin; Barata, Patrícia; Prata, José V.Derivatives of p-tert-butylcalix[4,6,8]arene carboxylic acids were used for selective adsorption of myoglobin.Amixtureofmyoglobin,laccaseandperoxidase wasusedforextractionwithcalixarenesandonlymyoglobin was selectively extracted to organic media. Myoglobin and Mb c–calixarene exhibited pseudoactivity of peroxidase in aqueous and organic media. This protein-calixarene complex exhibited the highest specific activity of 1.37 × 10−1 U.mg protein−1 at initial pH 6.5 of myoglobin aqueous solution. Apparent kinetic parameters (V max, K m, k cat and k cat/K m) for the pseudoperoxidase activity were determined in organic media for different initial pH values of myoglobin aqueous solution by Michaelis-Menten plot. The stability of this complex was studied for different initial pH values and t1/2 values were obtained in the range of 3.5–5.2 days. The extracted Mb c in organic media was recovered into fresh aqueous solutions at alkaline pH with a recovery of pseudoperoxidase activity of over 100%.
- Synthesis, structure, and optical properties of an alternating calix[4]arene-based meta-linked phenylene ethynylene copolymerPublication . D. Barata, Patrícia; Costa, Alexandra; Ferreira, Luis F. V.; Prata, José VirgílioNovel alternating copolymers comprising biscalix[4]arene-p-phenylene ethynylene and m-phenylene ethynylene units (CALIX-m-PPE) were synthesized using the Sonogashira-Hagihara cross-coupling polymerization. Good isolated yields (60-80%) were achieved for the polymers that show M-n ranging from 1.4 x 10(4) to 5.1 x 10(4) gmol(-1) (gel permeation chromatography analysis), depending on specific polymerization conditions. The structural analysis of CALIX-m-PPE was performed by H-1, C-13, C-13-H-1 heteronuclear single quantum correlation (HSQC), C-13-H-1 heteronuclear multiple bond correlation (HMBC), correlation spectroscopy (COSY), and nuclear overhauser effect spectroscopy (NOESY) in addition to Fourier transform-Infrared spectroscopy and microanalysis allowing its full characterization. Depending on the reaction setup, variable amounts (16-45%) of diyne units were found in polymers although their photophysical properties are essentially the same. It is demonstrated that CALIX-m-PPE does not form ground-or excited-state interchain interactions owing to the highly crowded environment of the main-chain imparted by both calix[4]arene side units which behave as insulators inhibiting main-chain pi-pi staking. It was also found that the luminescent properties of CALIX-m-PPE are markedly different from those of an all-p-linked phenylene ethynylene copolymer (CALIX-p-PPE) previously reported. The unexpected appearance of a low-energy emission band at 426 nm, in addition to the locally excited-state emission (365 nm), together with a quite low fluorescence quantum yield (Phi = 0.02) and a double-exponential decay dynamics led to the formulation of an intramolecular exciplex as the new emissive species.
- 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.
- New entities for sensory chemistry based on calix[4]arene-carbazole conjugates: from synthesis to applicationsPublication . Barata, Patrícia; Prata, José VirgílioTwo new calix[4]arene-carbazole conjugates (CALIX-CBZs) comprising 2- and 3-ethynyl-substituted carbazole derivatives attached to a central bis-calix[4]arene-containing phenylene ring have been designed for fluorescence-based detection of high explosive materials and explosive markers in vapour phase. The title compounds were prepared in good isolated yields and structurally fully characterised. CALIX-CBZs are highly fluorescent compounds that largely preserve their deep blue luminescence in solid state with no notorious emissions from electronic aggregated states. The excellent optical properties exhibited by casted films of both materials, including their photochemical stability, suggested their potential use as solidstate sensors. Remarkable high and fast responses were in fact retrieved upon contact with saturated vapours of 2,4,6trinitrotoluene (TNT, a high explosive) and 2,4-dinitrotoluene (a common impurity in TNT batches, often used as its chemical marker), reaching near 80% of fluorescence quenching for the later on 30s of exposure. Experiments performed with nitroaliphatic compounds (nitromethane (NM), a liquid explosive and 2,3-dimethyl-2,3-dinitrobutane, an explosive taggant) also revealed a high level of sensitivity (up to near 40% fluorescence quenching in only 10s of exposure to NM). The quenching efficiencies were overall correlated with the extent and strength of CALIX-CBZs–analyte interactions, the vapour pressure of the analytes and the film thicknesses.
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