Jaı̈rton Dupont

ORCID: 0000-0003-3237-0770
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About
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Research Areas
  • Ionic liquids properties and applications
  • Catalytic Cross-Coupling Reactions
  • Catalytic C–H Functionalization Methods
  • Advanced Photocatalysis Techniques
  • Electrochemical Analysis and Applications
  • Catalytic Processes in Materials Science
  • Asymmetric Hydrogenation and Catalysis
  • Carbon dioxide utilization in catalysis
  • Organometallic Complex Synthesis and Catalysis
  • Nanomaterials for catalytic reactions
  • Catalysis for Biomass Conversion
  • CO2 Reduction Techniques and Catalysts
  • Catalysis and Oxidation Reactions
  • TiO2 Photocatalysis and Solar Cells
  • Oxidative Organic Chemistry Reactions
  • Inorganic and Organometallic Chemistry
  • Chemical Synthesis and Reactions
  • Electrochemical sensors and biosensors
  • Synthetic Organic Chemistry Methods
  • Innovative Microfluidic and Catalytic Techniques Innovation
  • Sulfur-Based Synthesis Techniques
  • Conducting polymers and applications
  • Asymmetric Synthesis and Catalysis
  • Coordination Chemistry and Organometallics
  • Catalytic Alkyne Reactions

Universidade Federal do Rio Grande do Sul
2015-2024

Universidad de Murcia
2020-2024

University of Rio Grande and Rio Grande Community College
2014-2023

Universidade Federal do Rio Grande
2002-2023

University of Nottingham
2014-2020

Institute of Catalysis and Petrochemistry
2020

Center for Effective Philanthropy
2018

Park University
2015-2017

Jain University
2015

Universitat Autònoma de Barcelona
2015

1-n-Butyl-3-methylimidazolium hexafluorophosphate room-temperature ionic liquid is not only suitable as a medium for the preparation and stabilization of iridium nanoparticles but also ideal generation recyclable biphasic catalytic systems hydrogenation reactions. Thus, Ir(0) with mean diameter 2 nm have been prepared by reduction Ir(I) dissolved in H2. This solution can be reused several times olefins under mild reaction conditions.

10.1021/ja025818u article EN Journal of the American Chemical Society 2002-03-29

The electrochemical properties of the room temperature ionic liquids 1-butyl-3-methylimidazolium tetrafluoroborate (BMIM+BF4−), hexafluorophosphate (BMIM+PF6−) and 1-methyl-3-[2,6-(S)-dimethylocten-2-yl]imidazolium (MDIM+BF4−) as solvents have been studied using micro-samples, with a volume 10 μL, under vacuum conditions controlled gas moisture supplies. impact water—absorbed into liquid in manner from phase—on voltammetry dissolved redox systems on accessible potential window was...

10.1039/b007172m article EN New Journal of Chemistry 2000-01-01

Abstract Metal nanoparticles (MNPs) with a small diameter and narrow size distribution can be prepared by H 2 reduction of metal compounds or decomposition organometallic species dissolved in ionic liquids (ILs). MNPs dispersed ILs are catalysts for reactions under multiphase conditions. These soluble possess pronounced surfacelike rather than single‐site like catalytic properties. In other cases the not stable tend to aggregate serve as reservoirs mononuclear catalytically active species.

10.1002/chem.200601438 article EN Chemistry - A European Journal 2006-11-20

Nitrogen-, phosphorus-, and sulfur-containing palladacycles, typically containing four- or six-electron donor anionic metallated ligands, are emerging as a new family of organometallic catalyst precursors. These thermally air-stable complexes easy to handle their synthesis is often straightforward. Palladacycles now being successfully exploited in catalytic reactions ranging from classical hydrogenations enantioselective aldol-type condensations. The main recent achievements pertaining use...

10.1002/1099-0682(200108)2001:8<1917::aid-ejic1917>3.0.co;2-m article EN European Journal of Inorganic Chemistry 2001-08-01

Ionic liquids (ILs), a special group of classical molten salts, are widely used in various fields science. Historically, researchers have tested ILs out curiosity or to improve specific property particular system many areas chemistry materials However, today, far from being simple chemical curiosities and sit at the center green industrial innovation processes, where they play important roles extraction, reactive catalytic supports, spatial devices, biotransformations. In this Account, we...

10.1021/ar2000937 article EN Accounts of Chemical Research 2011-07-19

Among the various properties exhibited by ionic liquids (ILs)--especially those based on imidazolium cation-their inherent patterns, very low vapour pressure and pronounced self-organization in solid, liquid even gas phase are particularly interesting since this allows use of these fluids as alternative complementary media to classical organic solvents water many applications. Hence, reaction paths that involve charge-separated intermediates or transition states accelerated--by lowering...

10.1039/b602046a article EN Physical Chemistry Chemical Physics 2006-01-01

The reaction of 1-n-butyl-3-methylimidazolium chloride (BMI.Cl) with sodium tetrafluoroborate or hexafluorophosphate affords the molten salts BMI.X (1, X= BF4 and 2, PF6). Compounds 1 2 are viscous liquids within a wide range temperature (down to 192 K). IR, NMR, density, viscosity conductivity measurements suggest that compound behaves quasi-molecular. Compound is quasi-molecular below 279 K, but at higher temperatures probably composed imidazolium ions in an extended hydrogen-bonded network.

10.1051/jcp:1998103 article EN Journal de Chimie Physique 1998-07-01

Stable transition-metal nanoparticles of the type [M(0)](n) are easily accessible through reduction Ir(I) or Rh(III) compounds dissolved in "dry" 1-n-butyl-3-methylimidazolium hexafluorophosphate ionic liquid by molecular hydrogen. The formation these is straightforward; they prepared dry whereas presence water causes partial decomposition with phosphates, HF and fluorides. Transmission electron microscopy (TEM) observations X-ray diffraction analysis (XRD) show [Ir(0)](n) [Rh(0)](n) 2.0-2.5...

10.1002/chem.200304753 article EN Chemistry - A European Journal 2003-07-11

Pd(0) nanoparticles with approximately 2 nm diameter, immobilized in 1-n-butyl-3-methylimidazolium hexafluorophosphate ionic liquid, are efficient catalyst precursors for coupling of aryl halides n-butylacrylate. In situ TEM analysis the liquid catalytic solution after reaction shows formation larger ( 6 nm). The palladium content organic phase during arylation was checked by ICP-AS and significant metal leaching (up 34%) from to at low substrate conversions drops 5-8% higher conversions....

10.1021/ja0430043 article EN Journal of the American Chemical Society 2005-02-18

The main "molecular" physicochemical aspects involved in the catalytic applications of "soluble" transition metal nanoparticles ionic liquids are used to explain their properties. In particular, a special view on concepts coordination catalysis is describe properties these nanoscale catalysts solution as well scope and limitations multiphase catalysis.

10.1021/cs200525e article EN ACS Catalysis 2011-12-16

Abstract 2,1,3‐Benzothiadiazole (BTD) is one of the most important nuclei used in chemistry photoluminescent compounds and applicable for light technology. The understanding its properties reactions fundamental design application these derivatives molecular organic electronic devices other technologies. As a result their potential as constituents light‐emitting diodes, solar cells, liquid crystals, dyes, photovoltaic many others, attention has been focused on BTD π‐extended with use this...

10.1002/ejoc.201201161 article EN European Journal of Organic Chemistry 2012-12-07

Several imidazolium ionic liquids display high efficiency as catalysts for the sequential oxidation of alkene and carboxylation epoxide.

10.1039/c4gc00127c article EN Green Chemistry 2014-01-01

The interplay among the properties of catalysts, substrates, products, and ionic liquids (ILs) for a desired selective reaction is presented with selected examples. A guide to select most adequate IL catalytic device proposed.

10.1039/d2gc04749g article EN Green Chemistry 2023-01-01

The reaction of Pt(2)(dba)(3) (dba = bis-dibenzylidene acetone) dispersed in room temperature 1-n-butyl-3-methylimidazolium (BMI) hexafluorophosphate ionic liquid with molecular hydrogen (4 atm) at 75 degrees C leads to stable and isolable nanometric Pt(0) particles. X-ray diffraction analysis (XRD) the material indicated that it is constituted Pt(0). Transmission electron microscopy (TEM) particles shows formation [Pt(0)](n) nanoparticles 2.0-2.5 nm diameter. A detailed examination imbibed...

10.1021/ic034453r article EN Inorganic Chemistry 2003-06-21

Palladium(II) compounds dissolved in 1-n-butyl-3-methylimidazolium tetrafluoroborate (BMI·BF4) ionic liquid are shown to be able catalyze the hydrodimerization of 1,3-butadiene. In most cases, only 1,3-butadiene dimer 1,3,6-octatriene and telomer octa-2,7-dien-1-ol have been obtained. The products' selectivity catalytic activity depend on reaction conditions. 1,3-Butadiene conversion up 28%, a turnover frequency (TOF) 118 h-1, 94% were achieved with (BMI)2PdCl4 BMI·BF4. TOF significantly...

10.1021/om970982p article EN Organometallics 1998-01-31

The nature of the interactions between 1,3-dialkylimidazolium cations and noncoordinating anions such as tetrafluoroborate, hexafluorophosphate, tetraphenylborate has been studied in solid state by X-ray diffraction analysis solution (1)H NMR spectroscopy, conductivity, microcalorimetry. In state, these compounds show an extended network hydrogen-bonded which one cation is surrounded at least three anion imidazolium cations. pure form, salts are better described polymeric supramolecules type...

10.1021/jp0452709 article EN The Journal of Physical Chemistry B 2005-02-17

NiCl(2)(PCy(3))(2) associated with PCy(3) promotes the selective cross-coupling of aryltosylates arylboronic acids under relatively mild reaction conditions, and a variety functional groups are tolerated in both arenes. This is one simplest most efficient experimental procedures for coupling aryl tosylates reported to date. Reaction: see text.

10.1021/ol016526l article EN Organic Letters 2001-08-21

Abstract The reaction of N ‐alkylimidazole with alkyl sulfonates at room temperature affords 1,3‐dialkylimidazolium alkanesulfonates as crystalline solids in high yields. alkanesulfonate anions can be easily substituted by a series other [BF 4 , PF 6 3 (CF 2 CF ) SO and N(CF ] simple anions, salts, or acids water temperature. Extraction dichloromethane, filtration through short basic alumina column solvent evaporation the desired ionic liquids 80–95% yield. purity (&gt;99.4%) these...

10.1002/adsc.200505295 article EN Advanced Synthesis & Catalysis 2006-01-01
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