Jokin Carrillo

ORCID: 0000-0001-9867-5628
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About
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Research Areas
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • Polymer Nanocomposites and Properties
  • Synthetic Organic Chemistry Methods
  • Ionic liquids properties and applications
  • Force Microscopy Techniques and Applications
  • Material Dynamics and Properties
  • Synthesis of heterocyclic compounds
  • Carbohydrate Chemistry and Synthesis
  • Advanced Polymer Synthesis and Characterization
  • Quantum Dots Synthesis And Properties
  • Chemical synthesis and pharmacological studies
  • Marine Sponges and Natural Products
  • Synthesis and biological activity
  • Luminescence and Fluorescent Materials
  • Gold and Silver Nanoparticles Synthesis and Applications
  • Surfactants and Colloidal Systems
  • Carbon Nanotubes in Composites
  • nanoparticles nucleation surface interactions
  • Organoboron and organosilicon chemistry
  • Nanotechnology research and applications
  • Electrohydrodynamics and Fluid Dynamics
  • Pickering emulsions and particle stabilization
  • Phosphorus compounds and reactions
  • Cellular Mechanics and Interactions

Oak Ridge National Laboratory
2017-2025

University of Sheffield
2016

Universitat de Barcelona
2011-2014

Abstract Ten borylated bipyridines (BOBIPYs) have been synthesized and selected structural modifications made that allow useful structure–optical property relationships to be gathered. These systems further investigated using DFT calculations spectroscopic measurements, showing blue green fluorescence with quantum yields up 41 %. They full mapping of the structure determine where functionalities can implemented, tune optical properties or incorporate linking groups. The best derivative was...

10.1002/chem.201601915 article EN Chemistry - A European Journal 2016-07-28

Abstract Amphiphilic charged oligomers (oligodimethylsiloxane – methylimidazolium cation, ODMS‐MIM (+) ), assemble into bilayers using the droplet interface bilayer (DIB) platform, possess similar size and functionality as phospholipid bilayers, but exhibit increased stability. The oligomer ionic headgroups (MIM ) are covalently bound to monodisperse, short‐chain ( n = 13) hydrophobic tails (ODMS). These self‐assemble monolayer brushes at oil–aqueous of water droplets that influenced by both...

10.1002/macp.202400337 article EN cc-by-nc Macromolecular Chemistry and Physics 2025-04-08

Abstract The self‐assembly of amphiphilic bottlebrush block copolymers (BCPs), featuring backbones densely grafted with two types side chains, is less well understood compared to linear BCPs. In particular, the solution tapered BCPs—cone‐shaped BCPs hydrophilic or hydrophobic tips—remains unexplored. This study investigates eight and four cylindrical varied ratios polystyrene (PS) poly(acrylic acid) (PAA) synthesized via sequential addition macromonomers using ring‐opening metathesis...

10.1002/anie.202500771 article EN cc-by-nc Angewandte Chemie International Edition 2025-04-25

Abstract The self‐assembly of amphiphilic bottlebrush block copolymers (BCPs), featuring backbones densely grafted with two types side chains, is less well understood compared to linear BCPs. In particular, the solution tapered BCPs—cone‐shaped BCPs hydrophilic or hydrophobic tips—remains unexplored. This study investigates eight and four cylindrical varied ratios polystyrene (PS) poly(acrylic acid) (PAA) synthesized via sequential addition macromonomers using ring‐opening metathesis...

10.1002/ange.202500771 article EN cc-by-nc Angewandte Chemie 2025-04-25

Aberrant activation of NLRP3 due to persistent tissue damage, misfolded proteins or crystal deposits has been linked multiple chronic inflammatory disorders such as cryopyrin-associated periodic syndrome (CAPS), neurodegenerative diseases, gouty arthritis, and numerous others. Hence, there an increasing interest in inhibitors therapeutics. A first generation bearing a sulfonylurea core MCC950 (developed by Pfizer) were discovered phenotypic screening, however their mode action was only...

10.1021/acs.jmedchem.4c01376 article EN Journal of Medicinal Chemistry 2024-11-25
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