Olivier Coulembier

ORCID: 0000-0001-5753-7851
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About
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Research Areas
  • biodegradable polymer synthesis and properties
  • Carbon dioxide utilization in catalysis
  • Advanced Polymer Synthesis and Characterization
  • Synthetic Organic Chemistry Methods
  • Organometallic Complex Synthesis and Catalysis
  • Organic Electronics and Photovoltaics
  • Conducting polymers and applications
  • Synthesis and properties of polymers
  • Click Chemistry and Applications
  • Analytical Chemistry and Chromatography
  • Mass Spectrometry Techniques and Applications
  • Polymer Surface Interaction Studies
  • Chemical Synthesis and Analysis
  • Polymer crystallization and properties
  • Polyoxometalates: Synthesis and Applications
  • Dendrimers and Hyperbranched Polymers
  • Hydrogels: synthesis, properties, applications
  • Ion-surface interactions and analysis
  • Catalytic Cross-Coupling Reactions
  • Organoboron and organosilicon chemistry
  • Force Microscopy Techniques and Applications
  • Block Copolymer Self-Assembly
  • Nanofabrication and Lithography Techniques
  • Porphyrin and Phthalocyanine Chemistry
  • Chemical Synthesis and Reactions

University of Mons
2015-2024

Material (Belgium)
2011-2024

Ingenierie des Materiaux polymeres
2015-2022

Center for Innovation
2010-2021

University of Warwick
2013

Laboratoire de Chimie
2010

Bulgarian Academy of Sciences
2009

Institute of Polymers
2009

Stanford University
2006-2007

University of Liège
2005

The role of the molecular weight in crystallization and melt memory poly(ε-caprolactone) (PCL) was investigated. To this end, 10 PCL samples synthetic commercial origin different chain ends, covering a number-average (Mn) range between 0.48 70.5 kg/mol, were analyzed. Polarized light optical microscopy, differential scanning calorimetry, small-angle X-ray scattering (SAXS) employed for in-depth characterization. thermal transitions, morphology, kinetics, structural parameters, effects...

10.1021/acs.macromol.3c00234 article EN cc-by Macromolecules 2023-06-07

Abstract We describe the organocatalytic depolymerization of poly(ethylene terephthalate) (PET), using a commercially available guanidine catalyst, 1,5,7‐triazabicyclo[4.4.0]dec‐5‐ene (TBD). Postconsumer PET beverage bottles were used and processed with 1.0 mol % (0.7 wt %) TBD excess amount ethylene glycol (EG) at 190 °C for 3.5 hours under atmospheric pressure to give bis(2‐hydroxyethyl) terephthalate (BHET) in 78% isolated yield. The catalyst efficiency was comparable other metal...

10.1002/pola.24551 article EN Journal of Polymer Science Part A Polymer Chemistry 2011-01-11

Sowing the seeds: A simple strategy based on self-seeding allows large single crystals of long regioregular poly(3-hexylthiophene) chains to be grown from solution. When appropriately crystallized, materials differing in their degrees regioregularity and molecular weights formed monoclinic form II with interdigitated hexyl side groups (see picture). Detailed facts importance specialist readers are published as "Supporting Information". Such documents peer-reviewed, but not copy-edited or...

10.1002/anie.201205653 article EN Angewandte Chemie International Edition 2012-09-28

3D patterning by means of probe-assisted thermal decomposition has been achieved on phthalaldehyde polymer films with 1 nm vertical resolution and 40 lateral resolution. Highly efficient is enabled a self-amplified depolymerization mechanism. Pixel writing speeds the order microseconds are demonstrated.

10.1002/adma.200904386 article EN Advanced Materials 2010-04-23

Aliphatic polycarbonates are often referenced for their interesting applications due to lower tendency undergo hydrolysis, Tg, and degradation in renewable resources. Their synthesis is described using a series of metal-free catalysts allowing preparation well-defined polymers terms molecular weights structures. Additionally, some highlights regarding biomedical such as drug targeting presented.

10.1039/c0py00211a article EN Polymer Chemistry 2010-09-25

Catalysts are commonly used in polymer synthesis. Traditionally, catalysts to be metallic compounds but some studies have pointed out their toxicity for human health and environment, the removal of metal impurities from synthetic is quite expensive. Organocatalysts been intensively synthesized now widely ring-opening polymerization (ROP) reactions address these issues. However, most them, there not any evidence safety. The present study attempts assess whether well-established organo-based...

10.1021/bm5015443 article EN Biomacromolecules 2014-12-09

Despite significant advances in organocatalysis, stereoselective polymerization reactions utilizing chiral organocatalysts have received very little attention, and much about the underlying mechanisms remains unknown. Here, we report that both commercially available (R,R)- (S,S)-enantiomers of thiourea-amine Takemoto's promote efficient control high isoselectivity at room temperature ring-opening (ROP) racemic lactide by kinetic resolution, yielding highly isotactic, semicrystalline...

10.1021/acsmacrolett.8b00852 article EN publisher-specific-oa ACS Macro Letters 2018-11-19

Abstract Since the time first synthetic macrocycles were observed as academic curiosities, great advances have been made. Thanks to development of controlled polymerization processes, new catalytic systems and characterization techniques during last decades, well‐defined cyclic polymers are now readily accessible. This further permits determination their unique set properties, mainly due lack chain ends, use for industrial applications can be foreshadowed. review aims give an overview on...

10.1002/pol.20200236 article EN Journal of Polymer Science 2020-05-26

Alcohol adducts of the N-heterocyclic carbene, 1,3,4-triphenyl-4,5-dihydro-1H-1,2-triazol-5-ylidene (NHC), function as excellent single-component catalyst/initiators for ring-opening polymerization lactide and β-butyrolactone. Their reversible dissociation at elevated temperatures generates alcohol triazolylidene carbene to provide a facile entry cyclic esters on demand. Under optimum conditions, adverse transesterification reactions are minimized, importantly, upon complete consumption...

10.1021/ma0611366 article EN Macromolecules 2006-07-26

It's all about control: Alcohol adducts of stable N-heterocyclic carbenes function as excellent single-component catalysts/initiators for the ring-opening polymerization lactide (see scheme). This can be reversibly terminated simply by modulating temperature. The use multifunctional macroinitiators enables synthesis more complex polymer architectures. Supporting information this article is available on WWW under http://www.wiley-vch.de/contents/jc_2002/2005/z500723_s.pdf or from author....

10.1002/anie.200500723 article EN Angewandte Chemie International Edition 2005-07-11

Abstract Verwechslung ausgeschlossen : Ein Wasserstoffbrückenmotiv, das auf hexafluorierten Alkoholfunktionen beruht (siehe Bild; rot O, gelb F), aktiviert elektrophile Substrate. Die katalytische Aktivität des Systems wurde an der Ringöffnungspolymerisation einer Vielzahl gespannter Heterocyclen demonstriert. Polymere mit vorhersagbarem Molekulargewicht, niedriger Polydispersität und verlässlichen Endgruppen wurden erhalten. magnified image

10.1002/ange.200901006 article DE Angewandte Chemie 2009-06-15

Ring closure click chemistry methods have been used to produce cyclic c-PLLA and c-PDLA of a number-average molecular weight close 10 kg/mol. The effects stereochemistry the polymer chains their topology on structure, nucleation, crystallization were studied in detail employing wide-angle X-ray scattering (WAXS), small-angle (SAXS), polarized light optical microscopy (PLOM), standard advanced differential scanning calorimetry (DSC). crystal structures linear PLAs are identical each other, no...

10.1021/acs.macromol.7b02638 article EN Macromolecules 2018-02-20

ADVERTISEMENT RETURN TO ISSUEPREVNoteNEXTProbe-Based Nanolithography: Self-Amplified Depolymerization Media for Dry LithographyOlivier Coulembier†, Armin Knoll‡*, David Pires‡, Bernd Gotsmann‡, Urs Duerig‡, Jane Frommer§, Robert D. Miller§, Philippe Dubois†, and James L. Hedrick§*View Author Information† Laboratory of Polymeric Composite Materials, Center Innovation Research in Materials Polymers (CIRMAP), University Mons, Place du Parc 23, 7000 Belgium‡ IBM Zurich Laboratory, Säumerstrasse...

10.1021/ma9019152 article EN Macromolecules 2009-12-11

The ability of ICl<sub>3</sub> to activate electrophilic substrates through halogen bonding and its catalytic activity towards the ring-opening polymerization L-lactide is demonstrated in this communication. Association techniques highlights production narrowly dispersed PLA predictable molecular weights from commercially available molecule.

10.1039/c0py00013b article EN Polymer Chemistry 2010-01-01

Abstract Nowadays, numerous experimental and theoretical studies are devoted to the research field of polythiophenes other electroconjugated polymers due huge potentialities those conducting polymers. Synthetic procedures now developed reach highest control over both polymerization analytical methodologies allowing an in‐depth straightforward characterization polymer samples without any required doubt. Mass spectrometry in particular MALDI‐ToF measurements definitively suitable meet...

10.1002/jms.1886 article EN Journal of Mass Spectrometry 2011-03-01

A polylactide-block-(dimethyl β-malic acid-co-β-butyrolactone)-block-polylactide (PLA-b-P(dMMLA-co-BL)-b-PLA) triblock copolymer has been synthesized according to a totally original three-step strategy. In first step, the ring-opening polymerization (ROP) of dimethyl benzyl β-malolactonate (dMMLABz) and β-butyrolactone (BL) carried out in toluene/t-BuOH solvent mixture at 80 °C by using ethylene glycol as initiator commercially available 1,3,4-triphenyl-4,5-dihydro-1H-1,2,4-triazol-5-ylidene...

10.1021/ma060552n article EN Macromolecules 2006-05-17

Abstract Well‐defined amphiphilic PCL‐ b ‐PDMAEMA block copolymers were successfully synthesized by a combination of ATRP and “click” chemistry following either commutative two‐step procedure or straightforward one‐pot process using CuBr · 3Bpy as the sole catalyst. Compared to traditional coupling method, combining click even in “one‐pot” allows preparation diblock characterized narrow molecular weight distribution quantitative conversion azides alkynes into triazole functions. Moreover,...

10.1002/marc.200700400 article EN Macromolecular Rapid Communications 2007-09-24

Novel well-defined amphiphilic poly(d-lactide)-b-poly(N,N-dimethylamino-2-ethyl methacrylate) (PDLA-b-PDMAEMA) and poly(l-lactide)-b-poly(N,N-dimethylamino-2-ethyl (PLLA-b-PDMAEMA) copolymers were obtained. The synthesis strategy consisted of a three-step procedure: (i) controlled ring-opening polymerization (ROP) (d- or l-)lactide initiated by Al(OiPr)3, followed (ii) quantitative conversion the polylactide (PLA) hydroxyl end-groups with bromoisobutyryl bromide (iii) atom transfer radical...

10.1021/bm801515c article EN Biomacromolecules 2009-03-30
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