Lucas Montero de Espinosa

ORCID: 0000-0003-3616-0287
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About
Contact & Profiles
Research Areas
  • Advanced Polymer Synthesis and Characterization
  • Polymer composites and self-healing
  • Synthetic Organic Chemistry Methods
  • biodegradable polymer synthesis and properties
  • Fuel Cells and Related Materials
  • Chemical Synthesis and Analysis
  • Supramolecular Self-Assembly in Materials
  • Silicone and Siloxane Chemistry
  • Organometallic Complex Synthesis and Catalysis
  • Carbon dioxide utilization in catalysis
  • Advanced Cellulose Research Studies
  • Conducting polymers and applications
  • Synthesis and properties of polymers
  • Natural Fiber Reinforced Composites
  • Polysaccharides and Plant Cell Walls
  • Polymer Surface Interaction Studies
  • Advanced materials and composites
  • Flame retardant materials and properties
  • Polydiacetylene-based materials and applications
  • Covalent Organic Framework Applications
  • Catalytic Cross-Coupling Reactions
  • Dendrimers and Hyperbranched Polymers
  • Model-Driven Software Engineering Techniques
  • Advanced Materials and Mechanics
  • Photopolymerization techniques and applications

Adolphe Merkle Institute
2014-2020

University of Fribourg
2014-2020

Fribourg Development Agency
2015

Karlsruhe Institute of Technology
2010-2013

University of Potsdam
2010-2011

Universitat Politècnica de València
2011

Max Planck Institute of Colloids and Interfaces
2010

Max Planck Society
2010

Universitat Rovira i Virgili
2008-2010

Already for a long time, plant oils and their derivatives have been used by polymer chemists due to renewable nature, world wide availability, relatively low price, rich application possibilities. Although many different synthetic approaches used, more recent examples are pointing in the direction of catalytic transformations other efficient reactions achieve sustainable production polymers from these resources. In this context, olefin metathesis, thiol–ene additions, processes can...

10.1016/j.eurpolymj.2010.11.020 article EN cc-by-nc-nd European Polymer Journal 2010-12-10

Solvent and radical initiator-free addition of thiols to terpenes ((R)-(+)- (S)-(−)-limonene (−)-β-pinene) are described as a simple approach obtain wide range alcohol and/or ester functionalized renewable monomers. (R)-(+)-Limonene (1) (2), presenting different reactivity at the endocyclic exocyclic double bonds, have yielded monoaddition or diaddition product by variation thiol feed ratio. In same manner, (−)-β-pinene (3) derived monomers been prepared. The thus obtained characterized,...

10.1021/ma201544e article EN Macromolecules 2011-08-18

Abstract Vegetable oils are excellent renewable raw materials for thermosetting polymers. By the direct polymerization of triglyceride C=C, we obtained organic‐inorganic hybrid with promising properties optical applications by hydrosilylation alkenyl‐terminated fatty acid derivatives. The presence double bonds in triglycerides makes it possible to attach some functional groups through chemical modification, and describe various pathways functionalizing acids. Epoxidation is one most...

10.1002/ejlt.200900096 article EN European Journal of Lipid Science and Technology 2009-09-30

Cellulose nanocrystals (CNCs) are widely studied as reinforcing fillers for polymers. In many cases the mechanical properties of polymer/CNC nanocomposites do not match theoretical predictions, arguably on account CNC aggregation. This problem can be mitigated through addition a small amount judiciously selected polymeric dispersant that also serves binder among CNCs. We show 1–5% w/w poly(vinyl alcohol) (PVA) has very significant impact poly(ethylene oxide-co-epichlorohydrin)/CNC...

10.1021/acs.macromol.6b02629 article EN Macromolecules 2017-03-10

Abstract Triglycerides with acrylate functionality were prepared from a new route that involves the singlet oxygen photooxygenation of high oleic sunflower oil and further reduction resulting hydroperoxide derivatives to mixture secondary allylic alcohols. These unsaturated alcohols can be reduced saturated two hydroxyl‐containing triglycerides functionalized as esters radically crosslinked in presence different amounts pentaerythritol tetraacrylate. The crosslinking reactions followed by...

10.1002/pola.23225 article EN Journal of Polymer Science Part A Polymer Chemistry 2009-01-08

Within the current contribution, we introduce two strategies for catalyst-free, modular, ambient temperature synthesis of ABC triblock copolymers via photoinduced Diels–Alder reactions. On one hand, 2-formyl-3-methylphenoxy (FMP) moiety (a second generation photoenol precursor) was employed orthogonal polymer–polymer conjugations using terminal acrylates diblock synthesized acyclic-diene-metathesis (ADMET) polymerizations to directly prepare copolymers. other disparate reactivity...

10.1021/ma3007043 article EN Macromolecules 2012-06-07

With the goal to push mechanical properties of reconfigurable supramolecular polymers toward those thermoset resins, we prepared and investigated a new family hydrogen-bonded polymer networks that are assembled from isophthalic acid-terminated oligo(bisphenol A-co-epichlorohydrin) different bipyridines. These materials display high storage moduli up 3.9 GPa, can be disassembled upon heating form melts with viscosity as low 2.1 Pa·s, fully reassemble cooling. We show readily reconfigured,...

10.1021/acs.macromol.6b01491 article EN Macromolecules 2016-10-10

Their dynamic and stimuli-responsive nature makes supramolecular bonds useful for the design of functional polymers with adaptable properties. The combination multiple types interactions in one material permits, principle, access to multistimuli, multiresponsive polymers, but examples solid materials which different have led orthogonal responses toward stimuli are rare. Here we report a new platform that involves two orthogonally bound networks. network components based on trifunctional...

10.1021/acs.macromol.8b00555 article EN Macromolecules 2018-07-26

Abstract The acyclic diene metathesis (ADMET) polymerization of a phosphorus‐containing α, ω ‐diene prepared from plant oil derived building block is reported. Different ruthenium based catalysts and conditions were tested to optimize the ADMET this monomer. Undecylenyl undecenoate was used as fully renewable comonomer obtain polyesters with different phosphorus contents increase content final polymers. Copolymerization caused marked variations in molecular weights leading 6 38 KDa. effect...

10.1002/pola.23620 article EN Journal of Polymer Science Part A Polymer Chemistry 2009-09-28

Abstract An α,ω‐diene containing hydroxyl groups was prepared from plant oil‐derived platform chemicals. The acyclic diene metathesis copolymerization (ADMET) of this monomer with a phosphorus‐containing (DOPO II), also oil derived, afforded series phosphorus linear polyesters, which have been fully characterized. backbone hydroxyls these polyesters acrylated and radically polymerized to produce crosslinked polymers. thermomechanical mechanical properties, the thermal stability, flame...

10.1002/pola.23887 article EN Journal of Polymer Science Part A Polymer Chemistry 2010-02-18

Control over molecular architectures obtained viaADMET polymerization is limited by the step-growth nature of this technique. A new approach to polycondensation method described allowing for synthesis diblock and star-shaped polymers with weight control using selectivity olefin cross-metathesis between acrylates terminal olefins.

10.1039/c0cc04161k article EN Chemical Communications 2010-12-07

Abstract An increasing number of reports on the syntheses carbohydrate‐ and plant oil‐based polymers has been published in ongoing efforts to produce plastic materials from renewable resources. Although many these are biodegradable this is a desirable property for certain applications, some cases non‐degradable needed long‐term use purposes. Polyolefins one most important classes that have already taken their places our daily life. On other hand, production relies fossil Therefore, within...

10.1002/marc.201100280 article EN Macromolecular Rapid Communications 2011-06-24

A new family of sulfur-containing plasticizers derived from fatty acids has been developed. The synthetic approach is based on the thiol–ene addition alkyl thiols to double bond technical oleic acid, followed by oxidation sulfide group either sulfoxide or sulfone groups. It found that both and derivatives are not suitable as due their unpleasant odor limited thermal stabilities. However, odorless, thermally stable, show plasticizing properties similar those established PVC such...

10.1039/c3gc42172d article EN Green Chemistry 2013-11-15

The stimuli responsiveness of supramolecular polymers has recently been exploited for the development adhesives that can be (de)bonded on demand when heated or exposed to UV light. However, it remains difficult combine competitive solid-state mechanical properties and very low melt viscosity in one material. Here we report a new polymer platform based soybean oil as multifunctional low-molecular-weight monomer (∼1500 g/mol) isophthalic acid (IPA) groups show hydrogen bonding promote...

10.1021/acsapm.9b00175 article EN publisher-specific-oa ACS Applied Polymer Materials 2019-04-29

Abstract A novel triglyceride containing α,β‐unsaturated ketone was prepared through photoperoxidation from high oleic sunflower oil by two steps one pot environmentally friendly procedure. This new enone‐containing crosslinked with diaminodiphenylmethane (DDM) via aza‐Michael addition. kinetic study of the reaction p ‐toluidine either methyl oleate or epoxidized oleate, as model compounds, allowed us to establish higher reactivity former, thus confirming this curing system an alternative...

10.1002/pola.22992 article EN Journal of Polymer Science Part A Polymer Chemistry 2008-09-15

Heck coupling reactions are introduced as a modular, very efficient and highly orthogonal method for polymer–polymer conjugation. Several diblock triblock copolymers (5200 Da ≤ Mn 17300 Da, 1.08 PDI 1.33) were prepared via of acrylate-terminated aryliodide-terminated polymers. The performed using the so-called Jeffery's conditions, which allowed use equimolar amounts reacting polymers low reaction temperatures. Acrylated poly(ethylene glycol) monomethyl ether (PEG), poly(ε-caprolactone)...

10.1039/c2sc20402a article EN Chemical Science 2012-01-01

A modular approach for the design of two-component supramolecular polymer (SMP) networks is reported. series materials was prepared by blending two (macro)monomers based on trifunctional poly(propylene oxide) (PPO) cores that were end-functionalized with hydrogen-bonding 2-ureido-4[1H]pyrimidinone (UPy) groups. One monomer a PPO core number-average molecular weight (Mn) 440 g mol-1. The SMP formed this building block glassy, brittle material glass transition temperature (Tg) about 86 °C....

10.1021/acsmacrolett.9b00710 article EN publisher-specific-oa ACS Macro Letters 2019-10-24

Cellulose nanocrystals (CNCs) are widely used as reinforcing fillers in polymers due to their exceptionally high stiffness and strength because the biological species from which they isolated represent renewable resources. However, aggregation of CNCs, is concomitant with limited reinforcement, often difficult avoid. One-component nanocomposites (OCNs) based on polymer-grafted nanoparticles can solve this problem approach affords, by design, materials no such possible. At same time, chain...

10.1021/acs.macromol.9b01612 article EN Macromolecules 2020-01-28

The Passerini three‐component reaction is applied to synthesize, in a one‐step procedure, diverse asymmetric α,ω‐dienes containing an acrylate and terminal olefin. Such monomers are well known undergo head‐to‐tail acyclic diene metathesis (ADMET) polymerization due the high cross‐metathesis selectivity between acrylates olefins. Additionally, amphiphilic block copolymers synthesized using monofunctional PEG 480 monoacrylate, which acts as selective chain‐transfer agent during process. Thus,...

10.1002/macp.201300517 article EN Macromolecular Chemistry and Physics 2013-10-17
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