José A. Pomposo

ORCID: 0000-0003-4620-807X
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Conducting polymers and applications
  • Advanced Polymer Synthesis and Characterization
  • Material Dynamics and Properties
  • Polymer crystallization and properties
  • Advanced Sensor and Energy Harvesting Materials
  • Polymer Nanocomposites and Properties
  • Polymer Surface Interaction Studies
  • Transition Metal Oxide Nanomaterials
  • Electrochemical sensors and biosensors
  • Pickering emulsions and particle stabilization
  • Organic Electronics and Photovoltaics
  • biodegradable polymer synthesis and properties
  • Surfactants and Colloidal Systems
  • Supramolecular Self-Assembly in Materials
  • Click Chemistry and Applications
  • Analytical Chemistry and Sensors
  • Ionic liquids properties and applications
  • Dendrimers and Hyperbranched Polymers
  • Luminescence and Fluorescent Materials
  • Synthesis and properties of polymers
  • Advanced biosensing and bioanalysis techniques
  • Gold and Silver Nanoparticles Synthesis and Applications
  • Electrochemical Analysis and Applications
  • Gas Sensing Nanomaterials and Sensors
  • Nanocluster Synthesis and Applications

Material Physics Center
2016-2025

Ikerbasque
2015-2024

University of the Basque Country
2015-2024

Donostia International Physics Center
2008-2024

Consejo Superior de Investigaciones Científicas
2011-2012

Centre for Electrochemical Technologies
1999-2009

Centre National de la Recherche Scientifique
2008

Laboratoire de Chimie des Polymères Organiques
2008

A.E. Favorsky Irkutsk Institute of Chemistry
2008

Cidete (Spain)
2002

The synthesis and radical polymerization of ionic liquids based on 1-vinyl imidiazole are described that led to a new family poly(1-vinyl-3-alkyl-imidazolium) halides. Interestingly, the solubility these polymers is easily tuned by simple anion-exchange reaction. With this method polyelectrolytes soluble in variety organic solvents such as acetone, 2-butanone, tetrahydrofuran prepared.

10.1002/pola.11015 article EN Journal of Polymer Science Part A Polymer Chemistry 2003-11-25

Different ionic liquids (ILs) have been used as dopants in conducting polymer aqueous dispersion (PEDOT:PSS) leading to films of PEDOT:PSS/IL with enhanced electrical conductivity (up 136 S cm-1). After the addition ILs, AFM images show a three-dimensional network highly PEDOT exhibiting preferred paths for charge carrier transport.

10.1021/cm070398z article EN Chemistry of Materials 2007-03-28

Three imidazolium-based ionic liquid (IL) monomers, namely, 3-(1-ethyl imidazolium-3-yl)propylmethacrylamido bromide (IL-1), 2-(1-methylimidazolium-3-yl)ethyl methacrylate (IL-2), and 2-(1-ethylimidazolium-3-yl)ethyl (IL-3), methacrylic acid (MAA) were polymerized by the reversible addition fragmentation chain transfer (RAFT) process in methanolic solutions at 70 °C, using either 2-cyanopropyl dithiobenzoate (CTA-1) or (4-cyanopentanoic acid)-4-dithiobenzoate (CTA-2) as agents (CTAs). Under...

10.1021/ma800677h article EN Macromolecules 2008-08-16

Single-chain nanoparticles (SCNPs) are unimolecular soft nano-objects, consisting of individual polymer chains collapsed to a certain degree by means intramolecular bonding. Many the potential applications SCNPs rely on their particular molecular architecture. Even if ultimate goal is produce globular protein-like nanoparticles, recent small-angle neutron scattering (SANS) and X-ray (SAXS) results-supported computer simulations-indicate that in solution actually adopt sparse configurations....

10.1021/mz500354q article EN ACS Macro Letters 2014-07-24

The development of simple, efficient, and robust strategies affording the facile construction biomimetic organocatalytic nano-objects is currently a subject great interest. Herein, new pathway to artificial organocatalysts based on partially collapsed individual soft displaying useful diverse catalytic functions reported. Single-chain polymer nanoparticles endowed with enzyme-mimetic activity synthesized following this route display (i) relatively extended morphology under good solvent...

10.1021/mz4003744 article EN ACS Macro Letters 2013-08-15

Mimicking the substrate specificity and catalytic activity of enzymes is great interest for different fields (e.g., chemistry, biology, nanomedicine). Enhanced reaction rates using artificial, enzyme-mimic catalysts based on a variety molecular structures nanoentities macrocyclic compounds, star helical polymers, dendrimers) have been previously reported. However, examples enzyme-sized soft entities displaying are certainly scarce. Herein, we report synthesis characterization single-chain...

10.1021/mz5001477 article EN ACS Macro Letters 2014-04-22

Dynamic covalent enamine cross-links facilitate the reversible structural interconversion of dynamic single-chain polymer nanoparticles into linear chains using pH as a trigger.

10.1039/c3cc48733d article EN Chemical Communications 2014-01-01

We report herein a very efficient synthesis strategy for the construction of artificial transient-binding protein-mimic nano-objects. Michael addition-mediated multidirectional self-assembly individual polymeric chains at r.t. leads to "Michael" nanocarriers that in solution resemble disordered multidomain proteins, as revealed by combination small angle neutron scattering measurements and coarse-grained molecular dynamics simulation results, whereas dry state adopt collapsed, globular...

10.1021/mz400173c article EN ACS Macro Letters 2013-05-20

This review summarizes the opportunities offered by internal and external confinement of single-chain nanoparticles (SCNPs) in catalysts, drug delivery, sensing, other emerging potential applications.

10.1039/d0mh00846j article EN Materials Horizons 2020-01-01

Photocatalyzed reactions of organic substances in aqueous media are challenging transformations, often because scarce solubility substrates and catalyst deactivation. Herein, we report single-chain nanoparticles, SCNPs, capable efficiently catalyzing four different "in water" by employing visible light as the only external energy source. Specifically, decorated a high-molecular-weight copolymer, poly(OEGMA300-r-AEMA), with iridium(III) cyclometalated complex pendants at varying content...

10.1021/jacs.4c02718 article EN cc-by Journal of the American Chemical Society 2024-04-19

Abstract Summary: In this work, we report the synthesis of a great variety polycations with varying counter‐anions. These new polymers were obtained by simple anion exchange reaction facilitated phase separation resulting products. This strategy has been successfully applied to three different polycations, poly(1‐vinyl‐3‐ethylimidazolium bromide) poly(ViEtIm + Br − ), poly(1‐ethyl‐4‐vinylpyridinium poly(ViEtPy and poly(methacryloyloxyethyltrimethylammonium chloride) poly(EMTMA Cl seven...

10.1002/macp.200400411 article EN Macromolecular Chemistry and Physics 2005-01-17

Novel epoxy-based blends containing 30 wt % star styrene-b-butadiene block copolymers epoxidized at several degrees (SepB) have been investigated in order to analyze the effect of epoxidation degree on ability these produce nanostructures inside epoxy matrix as well their network structure matrix. For neat styrene−butadiene (SB) and SepB15-modified systems, macroscopic phase separation was observed. The SepB 40−76 mol %, however, yielded hexagonally ordered formed by PS cylinders arranged...

10.1021/ma0515477 article EN Macromolecules 2006-02-22

Carbon nanotubes, gold nanorods, and silver nanoparticles can be transferred from water to organic solvents back again by using polymeric ionic liquids (PILs) as vehicles (see scheme). The PILs are able trap several nano-objects during their anion-exchange-induced precipitation in water. This reversible process provides a PIL/nano-object composite that is fully redispersible solvents.

10.1002/smll.200500373 article EN Small 2006-03-01

Abstract A highly efficient room‐temperature synthetic route to bioconjugable polymeric nanoparticles in the 5–20 nm size range based on single‐chain intramolecular click cycloaddition is described. It illustrated by preparing cross‐linked NPs from poly[MMA‐ co ‐(3‐azidopropyl methacrylate)‐ ‐(3‐trimethylsilyl‐propyn‐1‐yl methacrylate)] terpolymers using a one‐pot procedure and continuous addition technique. For with an excess of azide groups, aminoacid/PMMA were easily obtained performing...

10.1002/marc.200700877 article EN Macromolecular Rapid Communications 2008-03-27

We investigate, by means of computer simulations, the formation soft nanoparticles irreversible intramolecular cross-linking homofunctional polymer precursors in good solvent. Simulations reveal that early and intermediate stages process are dominated bonding at short contour distances. Because initial self-avoiding character precursor, long distances, which is efficient mechanism for global compactation, a rare event essentially occurs late stage cross-linking. Thus, with identical...

10.1021/ma4021399 article EN Macromolecules 2013-12-03

The added value behind reversible bonds is the possibility to develop responsive structurally dynamic materials, which can adapt their constitution and, hence, properties external stimuli. In recent years, much effort has been devoted design and synthesis of single‐chain polymer nanoparticles (SCNPs) that be reversibly assembled or disassembled in response environmental changes even structure through simple exchange reactions. Here, evolution relatively new field SCNPs constructed via...

10.1002/ppsc.201300245 article EN Particle & Particle Systems Characterization 2013-11-29

Inspired by the multifunctionality of vitamin D‐binding protein and multiple transient‐binding behavior some intrinsically disordered proteins (IDPs), a polymeric platform is designed, prepared, characterized for combined delivery dermal protective anticancer bioactive cargos on basis artificial single‐chain nano‐objects mimicking IDPs. For first time ever, simultaneous folic acid or B 9 , hinokitiol, relevant natural compound that exhibits activity against human malignant melanoma cells,...

10.1002/marc.201300562 article EN Macromolecular Rapid Communications 2013-09-23

We report a new strategy for the rapid, efficient synthesis of single-chain polymer nanoparticles (SCNPs) having nearly globular morphology in solution, by employing photoactivated radical-mediated thiol–yne coupling (TYC) reaction as driving force chain folding/collapse. Confirmation SCNP formation was carried out means combination complementary experimental techniques. Size exclusion chromatography (SEC), small-angle X-ray scattering (SAXS), and dynamic light (DLS) measurements revealed...

10.1021/ma5017133 article EN Macromolecules 2014-11-26

Abstract Single‐chain nanoparticles ( SCNPs ) are polymeric soft nano‐objects constructed via individual chain compaction which envisioned as versatile building blocks for the construction of future smart, biofunctional nanodevices. According to their morphology in solution, can be classified (i) sparse resembling intrinsically disordered proteins having local compact zones connected by flexible spacers and (ii) globular a more akin that found native, (i.e. enzymes). The objective this...

10.1002/pi.5078 article EN Polymer International 2016-01-23
Coming Soon ...