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  • Carbon dots from coffee grounds by a one-pot microwave-assisted method
    Publication . 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.
  • Carbon nanodots from olive mill wastewater: a sustainable route
    Publication . Sousa, D. A.; Costa, Alexandra; Alexandre, M. R.; Prata, José Virgílio
    Olive oils are obtained from the fruit of the olive tree (Olea europaea L.) by combined mechanical and physical operations. Portugal has a significant production of olive oil (76 k tonnes/year over the last 5 years, 2010-2015) [1]. Olive oil is typically obtained by two main processes: batch press and continuous centrifugation. Depending on the particular process used, 200-1600 L of olive mill wastewater (OMWW) is produced per tonne of processed olives. Taken the lowest of these values, an estimate points to around 15 million L of OMWW may be produced each year in Portugal. The OMWW exhibits very low biodegradability parameters which pose serious issues for its treatment. Sustainable production of high-valued carbon materials from industrial lowvalued and problematic wastes is particularly appealing and highly desirable.
  • Polímeros fluorescentes para a detecção de metais tóxicos
    Publication . 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).
  • A solid-state fluorescence sensor for nitroaromatics and nitroanilines based on a conjugated Calix[4]arene polymer
    Publication . Prata, José V.; Costa, Alexandra I.; Teixeira, Carlos
    A 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.
  • Metal ion recognition induced by calix[4]arene carbazole containing polymers
    Publication . D. Barata, Patrícia; Costa, Alexandra; Fialho, Carina B.; Prata, José Virgílio
    Sensing 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]arenes
    Publication . 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.
  • Solid-state sensory properties of Calix-Poly(Phenylene Ethynylene)s toward nitroaromatic explosives
    Publication . Costa, Alexandra; Pinto, Hugo D.; Ferreira, Luís F. V.; Prata, José Virgílio
    This study is primarily focused in establishing the solid-state sensory abilities of several luminescent polymeric calix[4]arene-based materials toward selected nitroaromatic compounds (NACs), creating the foundations for their future application as high performance materials for detection of high explosives. The phenylene ethynylene-type polymers possessing bis-calix[4]arene scaffolds in their core were designed to take advantage of the known recognition abilities of calixarene compounds toward neutral guests, particularly in solid-state, therefore providing enhanced sensitivity and selectivity in the sensing of a given analyte. It was found that all the calix[4]arene-poly(para-phenylene ethynylene)s here reported displayed high sensitivities toward the detection of nitrobenzene, 2,4-dinitrotoluene and 2,4,6-trinitrotoluene (TNT). Particularly effective and significant was the response of the films (25-60 nm of thickness) upon exposure to TNT vapor (10 ppb): over 50% of fluorescence quenching was achieved in only 10 s. In contrast, a model polymer lacking the calixarene units showed only reduced quenching activity for the same set of analytes, clearly highlighting the relevance of the macrocyclics in promoting the signaling of the transduction event. The films exhibited high photostability (less than 0.5% loss of fluorescence intensity up to 15 min of continuous irradiation) and the fluorescence quenching sensitivity could be fully recovered after exposure of the quenched films to saturated vapors of hydrazine (the initial fluorescence intensities were usually recovered within 2-5 min of exposure to hydrazine).
  • Finding value in wastewaters from the cork industry: carbon dots synthesis and fluorescence for hemeprotein detection
    Publication . 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.
  • Chiroptical and emissive properties of a calix[4]arene-containing chiral poly (P-phenylene ethynylene) with enantioselective recognition ability
    Publication . Prata, José Virgílio; Costa, Alexandra; Pescitelli, Gennaro; Pinto, Hugo D.
    Supramolecular chirality was achieved in solutions and thin films of a calixarene-containing chiral aryleneethynylene copolymer. The observed chiroptical activity, which is primarily allied with the formation of aggregates of high molecular weight polymer chains, is the result of a combination of intrachain and interchain effects. The former arises by the adoption of an induced helix-sense by the polymer main-chain while the latter comes from the exciton coupling of aromatic backbone transitions. The co-existence of bulky bis-calixKlarene units and chiral side-chains on the polymer skeleton prevents efficient pi-stacking of neighbouring chains, keeping the chiral assembly highly emissive. In contrast, for a model polymer lacking calixarene moieties, the chiroptical activity is dominated by strong interchain exciton couplings as a result of more favourable packing of polymer chains, leading to a marked decrease of photoluminescence in the aggregate state. The enantiomeric recognition abilities of both polymers towards (R)- and (S)-alpha-methylbenzylamine were examined. It was found that a significant enantiodiscrimination is exhibited by the calixarene-based polymer in the aggregate state.
  • Carbon dots synthesis from coffee grounds, and sensing of nitroanilines
    Publication . 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.