65 results on '"Ronconi, Célia M."'
Search Results
52. Guanidine-functionalized Fe3O4 magnetic nanoparticles as basic recyclable catalysts for biodiesel production.
- Author
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Santos, Evelyn C. S., dos Santos, Thiago C., Guimarães, Renato B., Ishida, Lina, Freitas, Rafael S., and Ronconi, Célia M.
- Published
- 2015
- Full Text
- View/download PDF
53. Pseudorotaxanes and Rotaxanes Formed by Viologen Derivatives
- Author
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Braunschweig, Adam B., primary, Ronconi, Célia M., additional, Han, Ja‐Young, additional, Aricó, Fabio, additional, Cantrill, Stuart J., additional, Stoddart, J. Fraser, additional, Khan, Saeed I., additional, White, Andrew J. P., additional, and Williams, David J., additional
- Published
- 2006
- Full Text
- View/download PDF
54. Operating Molecular Elevators
- Author
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Badjic, Jovica D., primary, Ronconi, Célia M., additional, Stoddart, J. Fraser, additional, Balzani, Vincenzo, additional, Silvi, Serena, additional, and Credi, Alberto, additional
- Published
- 2006
- Full Text
- View/download PDF
55. Preparation and characterization of Cd2Nb2O7 thin films on Si substrates
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Ronconi, Célia M., Gonçalves, Débora, Suvorova, Nathalia, Alves, Oswaldo L., and Irene, Eugene A.
- Subjects
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THIN films , *CERAMICS , *ORGANOMETALLIC compounds , *NANOSTRUCTURES , *DIELECTRICS , *SILICON , *X-ray diffraction - Abstract
Abstract: Thin Cd2Nb2O7 films were grown on single-crystal p-type SiO2/Si substrates by the metallo-organic decomposition (MOD) technique. The films were investigated by X-ray diffraction, X-ray energy-dispersive spectroscopy, and field emission scanning electron microscopy, and showed a single phase (cubic pyrochlore), a crack-free spherical grain structure, and nanoparticles with a mean size of about 68nm. A Cauchy model was also used in order to obtain the thickness and index of refraction of the stack layers (transparent layer/SiO2/Si) by spectroscopic ellipsometry (SE). The dielectric constant (K) of the films was calculated to be about 25 from the capacitance–voltage (C–V) measurements. [Copyright &y& Elsevier]
- Published
- 2009
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56. Kinetic and mechanistic aspects for the tartaric acid oxidation by vanadium(V) in sulfuric acid medium
- Author
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Takashima, Keiko, Ziglio, Cláudio M., and Ronconi, Célia M.
- Abstract
Tartaric acid oxidation by vanadium(V) in sulfuric acid medium was investigated spectrophotometrically at 760 nm and 30°C by appearance of the vanadium(IV), as vanadyl. The reaction rate was determined under pseudo-first-order conditions with an excess of hydroxyacid over the oxidant concentration. The oxidation showed a first-order dependence with respect to vanadium(V) concentration and fractional orders with respect to tartaric acid and sulfuric acid concentrations, with no control and with constant ionic strength. The reaction rate is enhanced by an increase of ionic strength, and slightly reduced by a decrease of the dielectric constant of the medium. The activation parameters were calculated based on the rate constants determined in the 293 to 313 K interval. The proposed oxidation mechanisms and the derived rate laws are consistent with the experimental rate laws. © 1998 John Wiley & Sons, Inc. Int J Chem Kinet: 30: 5561, 1998.
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- 1998
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57. 3D Graphene‐Like Carbon Structures from Poly(Acrylic Acid): A Novel Synthetic Route.
- Author
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Simões, Ana L. A., Carvalho, Lílian A., Lago, Rochel M., Ronconi, Célia M., Vieira, Sara S., and Araujo, Maria H.
- Subjects
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EMERGING contaminants , *CARBON-based materials , *ACTIVATED carbon , *WATER purification , *ADSORPTION capacity - Abstract
Emerging contaminants, such as the hormone 17α‐ethynylestradiol (EE), in aquatic environments pose a serious risk to both human and environmental health, making efficient removal essential. This study evaluated the effectiveness of three‐dimensional porous carbon structures derived from poly(acrylic acid) (PAAc, Carbopol 990) as adsorbents for removing EE from aqueous solutions. Activated carbon materials were prepared using varying ratios of KOH as an activating agent (PAAc : KOH; 1 : 0 AAC, 1 : 1 AC1, 1 : 2 AC2, and 1 : 3 AC3). Adsorption tests were conducted by adding 10 mg of the adsorbent to 40 mL of an EE solution (100 ppm, 20 % acetonitrile in water). Analyses including TGA, XRD, and Raman spectroscopy were performed to evaluate the materials’ structural properties and adsorption capacities. Among the materials, AC3 exhibited the highest adsorption capacity for EE (238 mg g−1), followed by AC2 (153 mg g−1) and AC1 (82 mg g−1). The superior efficiency of AC3 can be attributed to its larger surface area and pore volume, enabling greater interaction with EE molecules. These materials demonstrated higher adsorption capacities compared to commercial activated carbons and single‐walled carbon nanotubes. This work opens new possibilities for developing efficient adsorbents, contributing to more effective and sustainable solutions for water purification and environmental protection. [ABSTRACT FROM AUTHOR]
- Published
- 2024
- Full Text
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58. CO2and H2adsorption on 3D nitrogen-doped porous graphene: Experimental and theoretical studies
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dos Santos, Thiago C., Mancera, Rafael C., Rocha, Marcus V.J., da Silva, Aline F.M., Furtado, Isabelle O., Barreto, Jade, Stavale, Fernando, Archanjo, Braulio S., de M. Carneiro, José Walkimar, Costa, Luciano T., and Ronconi, Célia M.
- Published
- 2021
- Full Text
- View/download PDF
59. Reversible single-crystal to single-crystal phase transformation between a new werner clathrate and its apohost†
- Author
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SFI, European Union (EU), CNPq (Conselho Nacional de Desenvolvimento Científico e Tecnológico – www.cnpq.br), Matos, Catiúcia R. M. O., Sanii, Rana, Wang, Shi-Qiang, Ronconi, Célia M., Zaworotko, Michael J., SFI, European Union (EU), CNPq (Conselho Nacional de Desenvolvimento Científico e Tecnológico – www.cnpq.br), Matos, Catiúcia R. M. O., Sanii, Rana, Wang, Shi-Qiang, Ronconi, Célia M., and Zaworotko, Michael J.
- Abstract
peer-reviewed, In this work, we report the synthesis and structural characterisation of the ligand 2(pyridin-3-yl)-benzo [de]isoquinoline-1,3(2H)-dione, 5, its isostructural Werner complexes ML4(NCS)2 (L = 5; M = Co(II) and Ni (II)), and five clathrates with three aromatic guests, ML4(NCS)2·2G (M = Co(II) and Ni(II), G = nitrobenzene (NB); M = Co, G = 1,2 dichlorobenzene (1,2-DCB); M = Co(II) and Ni(II), G = o-xylene (OX)). 5 was pre-pared in high yield by condensation in the solid-state (C3S3, Cocrystal Controlled Solid-State Synthesis). The Werner complexes ML4(NCS)2 (M = Co(II) and Ni(II)) (apohosts) were prepared by reacting M(NCS)2 (M = Co(II) and Ni(II)) and 5 in 1-butanol at 60 °C for 24 h. The Werner clathrates were prepared by reacting M(NCS)2 (M = Co(II) and Ni(II)), G and 5 in 1-butanol at 60 °C for 48–96 h. The clathrates were observed to transform to the apohost ML4(NCS)2 upon heating. CoL4(NCS)2·2NB was subsequently regenerated by exposing CoL4(NCS)2 to liquid NB at 60 °C for 48 h. This phase change occurred as a single-crystal to single-crystal phase transformation and was studied by single crystal X-ray diffraction, powder X-ray diffraction and thermal analyses. Structural analyses of the apohost CoL4(NCS)2 and its Werner clathrate CoL4(NCS)2·2NB indicated that rotational freedom of the Co-N bonds together with torsional flexibility of the ligand between the imide bond and the pyridine moiety are key to enabling the structural switching induced by exposure to NB or its removal
60. Polyviologen dendrimers as hosts and charge-storing devices
- Author
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Massimo Baroncini, Paola Ceroni, Vincenzo Balzani, Margherita Venturi, Carlo Giansante, Célia M. Ronconi, J. Fraser Stoddart, C.M. Ronconi, J.F. Stoddart, V. Balzani, M. Baroncini, P. Ceroni, C. Giansante, M. Venturi, Ronconi, Célia M, Stoddart, J. Fraser, Balzani, Vincenzo, Baroncini, Massimo, Ceroni, Paola, Giansante, Carlo, and Venturi, Margherita
- Subjects
Chemistry ,Stereochemistry ,Dendrimer ,Organic Chemistry ,General Chemistry ,Medicinal chemistry ,Signal amplification ,Catalysis - Abstract
Two dendrimers were designed and synthesized that contain a 1,3,5-trisubstituted benzenoid core and incorporate 9 and 21 viologen (4,4′-bipyridinium) units in their branches in addition to hydrophilic (aryloxy) terminal groups. For comparison purposes, model compounds containing one and two viologen units were also studied. These polycationic dendrimers form strong host–guest complexes with the dianionic form of the red dye eosin in dilute CH2Cl2 solutions. Titration experiments, based on fluorescence measurements, showed that each viologen unit in the dendritic structures becomes associated with an eosin dianion. Electrochemical (in MeCN) and photosensitization (in CH2Cl2) experiments revealed that only a fraction of the viologen units present in the dendritic structures can be reduced. This fraction corresponds to the number of viologen units present in the outer shells of the dendrimers. The reasons for incomplete charge pooling are discussed. Comparison with the behavior of polyviologen dendrimers that are terminated with bulky tetraarylmethane groups and were studied previously enabled the role played by the terminal groups in the redox and hosting properties to be elucidated. Sono stati progettati e sintetizzati due dendrimeri contenenti un'unita benzenica sostituita nelle posizioni 1,3,5 come core, 9 e 21 unita viologeno (4,4′-dipiridinio), rispettivamente, nelle ramificazioni e gruppi idrofilici di tipo arilossi come unita periferiche. In CH2Cl2 questi dendrimeri policationici interagiscono con la forma dianionica dell'eosina dando complessi host–guest in cui, come mostrato chiaramente dalle titolazioni basate su misure di fluorescenza, ogni unita viologeno contenuta nella struttura dendritica si associa con un anione eosina. Esperimenti di riduzione elettrochimica (in MeCN) e fotochimica (in CH2Cl2 e in presenza di un opportuno fotosensibilizzatore) hanno inoltre messo in evidenza che non tutte le unita viologeno contenute nei dendrimeri possono essere ridotte; in particolare, sembra che siano riducibili solo quelle presenti nel guscio dendritico piu esterno. Il confronto con il comportamento di composti modello, contenenti una e due unita viologeno, e di dendrimeri precedentemente investigati, che differiscono da quelli discussi in questo lavoro per la presenza di gruppi terminali piu ingombranti di tipo tetraarilmetano, ha fatto luce sui motivi che inibiscono la riduzione di tutte le unita viologeno contenute nelle strutture dendritiche e ha chiarito se e come la natura dei gruppi terminali influenza le proprieta redox e complessanti di questi dendrimeri.
- Published
- 2008
61. Zika Virus NS1 Protein Detection Using Gold Nanoparticle-Assisted Dynamic Light Scattering.
- Author
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D'Amato DL, Bessa IAA, Souza ABC, Mendes-Monteiro L, Mohana-Borges R, Allonso D, Ligiero CBP, and Ronconi CM
- Subjects
- Antibodies, Monoclonal chemistry, Antibodies, Monoclonal immunology, Limit of Detection, Humans, Metal Nanoparticles chemistry, Gold chemistry, Zika Virus isolation & purification, Viral Nonstructural Proteins analysis, Viral Nonstructural Proteins immunology, Dynamic Light Scattering, Biosensing Techniques methods
- Abstract
The Zika virus (ZIKV) is a global health threat due to its rapid spread and severe health implications, including congenital abnormalities and neurological complications. Differentiating ZIKV from other arboviruses such as dengue virus (DENV) is crucial for effective diagnosis and treatment. This study presents the development of a biosensor for detecting the ZIKV non-structural protein 1 (NS1) using gold nanoparticles (AuNPs) functionalized with monoclonal antibodies employing dynamic light scattering (DLS). The biosensor named ZINS1-mAb-AuNP exhibited specific binding to the ZIKV NS1 protein, demonstrating high colloidal stability indicated by a hydrodynamic diameter (D
H ) of 140 nm, detectable via DLS. In the absence of the protein, the high ionic strength medium caused particle aggregation. This detection method showed good sensitivity and specificity, with a limit of detection (LOD) of 0.96 μg mL-1 , and avoided cross-reactivity with DENV2 NS1 and SARS-CoV-2 spike proteins. The ZINS1-mAb-AuNP biosensor represents a promising tool for the early and accurate detection of ZIKV, facilitating diagnostic and treatment capabilities for arboviral infections., (© 2024 Wiley-VCH GmbH.)- Published
- 2024
- Full Text
- View/download PDF
62. Innovating Leishmaniasis Treatment: A Critical Chemist's Review of Inorganic Nanomaterials.
- Author
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Bessa IAA, D'Amato DL, C Souza AB, Levita DP, Mello CC, da Silva AFM, Dos Santos TC, and Ronconi CM
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- Humans, Animals, Drug Delivery Systems, Leishmaniasis drug therapy, Leishmaniasis parasitology, Nanostructures therapeutic use, Leishmania drug effects, Antiprotozoal Agents therapeutic use, Antiprotozoal Agents pharmacology
- Abstract
Leishmaniasis, a critical Neglected Tropical Disease caused by Leishmania protozoa, represents a significant global health risk, particularly in resource-limited regions. Conventional treatments are effective but suffer from serious limitations, such as toxicity, prolonged treatment courses, and rising drug resistance. Herein, we highlight the potential of inorganic nanomaterials as an innovative approach to enhance Leishmaniasis therapy, aligning with the One Health concept by considering these treatments' environmental, veterinary, and public health impacts. By leveraging the adjustable properties of these nanomaterials─including size, shape, and surface charge, tailored treatments for various diseases can be developed that are less harmful to the environment and nontarget species. We review recent advances in metal-, oxide-, and carbon-based nanomaterials for combating Leishmaniasis, examining their mechanisms of action and their dual use as standalone treatments or drug delivery systems. Our analysis highlights a promising yet underexplored frontier in employing these materials for more holistic and effective disease management.
- Published
- 2024
- Full Text
- View/download PDF
63. A Carbocationic Triarylmethane-Based Porous Covalent Organic Network.
- Author
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Freitas SKS, Oliveira FL, Dos Santos TC, Hisse D, Merlini C, Ronconi CM, and Esteves PM
- Abstract
A thermally stable carbocationic covalent organic network (CON), named RIO-70 was prepared from pararosaniline hydrochloride, an inexpensive dye, and triformylphloroglucinol in solvothermal conditions. This nanoporous organic material has shown a specific surface area of 990 m
2 g-1 and pore size of 10.3 Å. The material has CO2 uptake of 2.14 mmol g-1 (0.5 bar), 2.7 mmol g-1 (1 bar), and 6.8 mmol g-1 (20 bar), the latter corresponding to 3 CO2 molecules adsorbed per pore per sheet. It is shown to be a semiconductor, with electrical conductivity (σ) of 3.17×10-7 S cm-1 , which increases to 5.26×10-4 S cm-1 upon exposure to I2 vapor. DFT calculations using periodic conditions support the findings., (© 2020 Wiley-VCH GmbH.)- Published
- 2021
- Full Text
- View/download PDF
64. Degradation of magnetic nanoparticles mimicking lysosomal conditions followed by AC susceptibility.
- Author
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Gutiérrez L, Romero S, da Silva GB, Costo R, Vargas MD, Ronconi CM, Serna CJ, Veintemillas-Verdaguer S, and Del Puerto Morales M
- Subjects
- Biomimetic Materials chemistry, Biomimetic Materials radiation effects, Body Fluids chemistry, Coated Materials, Biocompatible chemistry, Coated Materials, Biocompatible radiation effects, Electric Impedance, Kinetics, Magnetite Nanoparticles radiation effects, Materials Testing, Particle Size, Temperature, Citric Acid chemistry, Lysosomes chemistry, Lysosomes ultrastructure, Magnetite Nanoparticles chemistry, Magnetite Nanoparticles ultrastructure, Phosphonoacetic Acid chemistry
- Abstract
Background: A deeper knowledge on the effects of the degradation of magnetic nanoparticles on their magnetic properties is required to develop tools for the identification and quantification of magnetic nanoparticles in biological media by magnetic means., Methods: Citric acid and phosphonoacetic acid-coated magnetic nanoparticles have been degraded in a medium that mimics lysosomal conditions. Magnetic measurements and transmission electron microscopy have been used to follow up the degradation process., Results: Particle size is reduced significantly in 24 h at pH 4.5 and body temperature. These transformations affect the magnetic properties of the compounds. A reduction of the interparticle interactions is observed just 4 h after the beginning of the degradation process. A strong paramagnetic contribution coming from the degradation products appears with time., Conclusions: A model for the in vivo degradation of magnetic nanoparticles has been followed to gain insight on the changes of the magnetic properties of iron oxides during their degradation. The degradation kinetics is affected by the particle coating, in our case being the phosphonoacetic acid-coated particles degraded faster than the citric acid-coated ones.
- Published
- 2015
- Full Text
- View/download PDF
65. Polyviologen dendrimers as hosts and charge-storing devices.
- Author
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Ronconi CM, Stoddart JF, Balzani V, Baroncini M, Ceroni P, Giansante C, and Venturi M
- Abstract
Two dendrimers were designed and synthesized that contain a 1,3,5-trisubstituted benzenoid core and incorporate 9 and 21 viologen (4,4'-bipyridinium) units in their branches in addition to hydrophilic (aryloxy) terminal groups. For comparison purposes, model compounds containing one and two viologen units were also studied. These polycationic dendrimers form strong host-guest complexes with the dianionic form of the red dye eosin in dilute CH(2)Cl(2) solutions. Titration experiments, based on fluorescence measurements, showed that each viologen unit in the dendritic structures becomes associated with an eosin dianion. Electrochemical (in MeCN) and photosensitization (in CH(2)Cl(2)) experiments revealed that only a fraction of the viologen units present in the dendritic structures can be reduced. This fraction corresponds to the number of viologen units present in the outer shells of the dendrimers. The reasons for incomplete charge pooling are discussed. Comparison with the behavior of polyviologen dendrimers that are terminated with bulky tetraarylmethane groups and were studied previously enabled the role played by the terminal groups in the redox and hosting properties to be elucidated.
- Published
- 2008
- Full Text
- View/download PDF
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