Vincent Darcos

ORCID: 0000-0003-0031-0984
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Research Areas
  • biodegradable polymer synthesis and properties
  • Advanced Polymer Synthesis and Characterization
  • Polymer Surface Interaction Studies
  • Bone Tissue Engineering Materials
  • Radioactive element chemistry and processing
  • Nanoparticle-Based Drug Delivery
  • Click Chemistry and Applications
  • Chemical Synthesis and Characterization
  • Hydrogels: synthesis, properties, applications
  • Medical Imaging Techniques and Applications
  • Lanthanide and Transition Metal Complexes
  • Porphyrin and Phthalocyanine Chemistry
  • Molecular Sensors and Ion Detection
  • Luminescence and Fluorescent Materials
  • Graphene and Nanomaterials Applications
  • Nuclear Materials and Properties
  • Polysaccharides and Plant Cell Walls
  • Fuel Cells and Related Materials
  • Facial Trauma and Fracture Management
  • Oral health in cancer treatment
  • Advanced MRI Techniques and Applications
  • Antimicrobial agents and applications
  • Silicone and Siloxane Chemistry
  • Synthetic Organic Chemistry Methods
  • Analytical Chemistry and Chromatography

Institut des Biomolécules Max Mousseron
2015-2025

Université de Montpellier
2011-2024

Centre National de la Recherche Scientifique
2010-2024

Institut Européen des Membranes
2024

École Nationale Supérieure de Chimie de Montpellier
2016-2024

Bipar
2016

Institut des Sciences Moléculaires
2009

École Nationale Supérieure de Chimie, de Biologie et de Physique
2004

University of Warwick
2003-2004

Laboratoire de Chimie des Polymères Organiques
2004

Diffusion-ordered spectroscopy (DOSY) NMR was successfully used to characterize amphiphilic block copolymers. A triblock copolymer prepared by ring-opening polymerisation of a lactide using poly(ethylene glycol) as the initiator. The DOSY experiment is revealed be useful analytical method prove formation According map, PLA and PEG blocks exhibited same diffusion coefficient 5.623 × 10−10 m2 s−1, consistent with an efficient lactide. determination critical micelle concentration (CMC)...

10.1039/c2py20054f article EN Polymer Chemistry 2012-01-01

Amphiphilic and cationic PCL-based degradable polyester was synthesized by copper-catalyzed azide-alkyne cycloaddition (CuAAC).

10.1039/c0py00004c article EN Polymer Chemistry 2010-01-01

ADVERTISEMENT RETURN TO ISSUEPREVCommunicationNEXTSupramolecular Catalysis of Olefin [2 + 2] PhotodimerizationDario M. Bassani, Vincent Darcos, Sarah Mahony, and Jean-Pierre DesvergneView Author Information Laboratoire de Chimie Organique et Organométallique CNRS UMR 5802 Université Bordeaux 1 33405 Talence Cedex, France Cite this: J. Am. Chem. Soc. 2000, 122, 36, 8795–8796Publication Date (Web):August 24, 2000Publication History Received12 June 2000Published online24 August inissue...

10.1021/ja002089e article EN Journal of the American Chemical Society 2000-08-24

Abstract The use of DMSO as solvent for transition metal mediated living radical polymerization was investigated using copper (I) bromide/N‐( n ‐propyl)‐2‐pyridyl‐methanimine catalyst system and ethyl‐2‐bromoisobutyrate initiator. best conditions in different methacrylates (MMA, BMA, DMAEMA, HEMA) were determined. In all cases, the measured number‐average molar mass product increased linearly with monomer conversion agreement theoretical M low polydispersity products (1.16 < PDI 1.4)...

10.1002/pola.20403 article EN Journal of Polymer Science Part A Polymer Chemistry 2004-11-03

A new functional lactone, α-iodo-ε-caprolactone (αIεCL), was synthesized from ε-caprolactone by anionic activation using a non-nucleophilic strong base (lithium diisopropylamide) followed an electrophilic substitution with iodine chloride. Ring-opening (co)polymerizations of the resulting monomer were carried out tin 2-ethylhexanoate as catalyst in toluene at 100 °C. Homopolymerization αIεCL achieved, and poly(αIεCL) fully characterized SEC, (1) H NMR elemental analysis. Random...

10.1002/marc.200800596 article EN Macromolecular Rapid Communications 2008-12-23

Well-defined graft copolymers were obtained using a copper-catalysed azide–alkyne Huisgen's cycloaddition click reaction from both biocompatible and non-toxic poly(ε-caprolactone) poly(2-methyl-2-oxazoline) homopolymers. Resulting amphiphilic proved to form micelles that could be used as potential drug carriers.

10.1039/c2cc30191a article EN Chemical Communications 2012-01-01

Silicate-based bioactive glass nano/microspheres hold significant promise for bone substitution by facilitating osteointegration through the release of biologically active ions and formation a biomimetic apatite layer. Cu-doping enhances properties such as pro-angiogenic antibacterial behavior. While sol-gel methods usually yield homogeneous spherical particles pure silica or binary glasses, synthesizing poorly aggregated Cu-doped ternary nano/microparticles without secondary CuO crystalline...

10.1016/j.actbio.2024.05.003 article EN cc-by-nc-nd Acta Biomaterialia 2024-05-07

A first generation phosphorus-containing dendrimer with twelve terminal benzyl dithiobenzoate functions was designed and subsequently used as a multifunctional agent to derive hybrid star copolymers consisting of dendritic core surrounded by polystyrene branches reversible addition-fragmentation chain transfer (RAFT).

10.1039/b407508k article EN Chemical Communications 2004-01-01

A new functional dilactone, 3-(2-propynyl)-1,4-dioxane-2,5-dione (4), was synthesized from ethyl glyoxalate and propargyl bromide via a 4-step reaction sequence. Ring-opening (co)polymerisation of the alkyne-functionalised monomer 4 with L-lactide carried out in dichloromethane at 30 °C using N,N-dimethylaminopyridine as catalyst benzyl alcohol an initiator. The resulting copolyesters were characterized by 1H NMR, size exclusion chromatography (SEC) MALDI-TOF spectroscopy. Azide...

10.1039/c3py00375b article EN Polymer Chemistry 2013-01-01

A straightforward approach based on thiol–ene click chemistry was used to prepare novel functional polyesters containing amino groups. First, a series of well-defined alkene-functional poly(ε-caprolactone)s were prepared by ring-opening polymerization α-allyl-ε-caprolactone with ε-caprolactone in toluene and bulk using tin 2-ethylhexanoate as catalyst. These fully characterized 1H NMR, GPC, MALDI-TOF MS. The resulting random copolyesters obtained wide range molar masses from 3000 50 000 g...

10.1039/c1py00414j article EN Polymer Chemistry 2011-11-21

Cancer vaccines are considered to be a promising tool for cancer immunotherapy. However, well-designed vaccine should combine tumor-associated antigen (TAA) with the most effective immunomodulatory agents and/or delivery system provoke intense immune responses against TAA. In present study, we introduced new approach by conjugating molecule LD-indolicidin hydrophilic chain end of polymeric emulsifier poly(ethylene glycol)-polylactide (PEG-PLA), allowing located close surface resulting...

10.1021/acs.biomac.5b01150 article EN Biomacromolecules 2015-10-16

ABSTRACT Novel thermo‐responsive poly( N ‐isopropylacrylamide)‐ block ‐poly( l ‐lactide)‐ ‐isopropylacylamide) (PNIPAAm‐ b ‐PLLA‐ ‐PNIPAAm) triblock copolymers were successfully prepared by atom transfer radical polymerization of NIPAAm with Br‐PLLA‐Br macroinitiator, using a CuCl/tris(2‐dimethylaminoethyl) amine (Me 6 TREN) complex as catalyst at 25 °C in , ‐dimethylformamide/water mixture. The molecular weight the ranges from 18,000 to 38,000 g mol −1 and dispersity 1.10 1.28. Micelles are...

10.1002/pola.26721 article EN Journal of Polymer Science Part A Polymer Chemistry 2013-05-16

Thermo-responsive P(NIPAAm-<italic>co</italic>-DMAAm)-<italic>b</italic>-PLLA-<italic>b</italic>-P(NIPAAm-<italic>co</italic>-DMAAm) triblock copolymers are synthesized <italic>via</italic> combination of ring-opening polymerization and atom transfer radical polymerization.

10.1039/c3tb21793k article EN Journal of Materials Chemistry B 2014-01-01

Abstract Novel 5‐ Z ‐amino‐δ‐valerolactone (5‐NHZ‐VL) was synthesized with an aim to prepare degradable polyesters and copolyesters having amino pendant groups. Following a straightforward efficient synthetic pathway, 5‐NHZ‐VL obtained in only two steps up 50% yield. The monomer fully characterized by 1 H NMR, 13 C ESI mass spectrometry, HPLC. Various conventional conditions were tested for this lactone ring‐opening polymerization led the novel corresponding poly(5‐NHZ‐VL) ( M n = 7000...

10.1002/pola.24400 article EN Journal of Polymer Science Part A Polymer Chemistry 2010-11-03

API-ILs were encapsulated into biocompatible PLLA. The morphology and crystallinity of the resulting membranes can be tuned by varying IL nature content leading to controlled release.

10.1039/c4tb00264d article EN Journal of Materials Chemistry B 2014-01-01

Hydrophobic macromolecular contrast agents (MMCAs) are highly desirable to provide safe and efficient magnetic resonance (MR) visibility implantable medical devices. In this study, we report on the synthesis evaluation of novel biodegradable poly(ε-caprolactone)-based MMCAs. Poly(α-propargyl-ε-caprolactone-co-ε-caprolactone)s containing 2, 5, 10 mol % propargyl groups have been prepared by ring-opening copolymerization ε-caprolactone corresponding propargylated lactone. parallel, a diazido...

10.1021/bm400978a article EN Biomacromolecules 2013-09-05

Abstract In situ Fourier transform near infrared (FTNIR) spectroscopy was successfully used to monitor monomer conversion during copper mediated living radical polymerization with N ‐( n ‐propyl)‐2‐pyridylmethanimine as a ligand. The of vinyl protons in methacrylic monomers (methyl methacrylate, butyl and ‐hydroxysuccinimide methacrylate) methylene the polymer monitored an inert fiber‐optic probe. monitoring poly(butyl methacrylate‐ b ‐methyl ‐butyl triblock copolymer has also been reported...

10.1002/pola.20308 article EN Journal of Polymer Science Part A Polymer Chemistry 2004-08-26
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