Rémi Auvergne

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Institut Charles Gerhardt Montpellier

Rémi Auvergne
Enseignant-Chercheur - MC, Equipe IAM
ENSCM
8 Rue Ecole Normale
34296 Montpellier Cedex 5

04 67 14 43 05
remi.auvergne@enscm.fr

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2019

Yvan Ecochard, Jules Leroux, Bernard Boutevin, Rémi Auvergne and Sylvain Caillol
From multi-functional siloxane-based cyclic carbonates to hybrid polyhydroxyurethane thermosets,
Eur. Polym. J. 2019, 120, 109280
Thi-Thanh-Tam Nguyen, Sabrina Belbekhouche, Rémi Auvergne, Benjamin Carbonnier and Daniel Grande
Controlled allylation of polyelectrolytes: a deep insight into chemical aspects and their applicability as building blocks for robust multilayer coatings,
Pure Appl. Chem. 2019, 91, 983-995
Mélanie Decostanzi, Rémi Auvergne, Bernard Boutevin and Sylvain Caillol
Biobased phenol and furan derivative coupling for the synthesis of functional monomers,
Green Chem. 2019, 21, 724-747

2017

Mélanie Decostanzi, Rémi Auvergne, Emilie Darroman, Bernard Boutevin and Sylvain Caillol
Reactivity and kinetics of HDI-iminooxadiazinedione, Application to polyurethane synthesis,
Eur. Polym. J. 2017, 96, 443-451
Marine Blain, Adrien Cornille, Bernard Boutevin, Rémi Auvergne, Dominique Benazet, Bruno Andrioletti and Sylvain Caillol
Hydrogen bonds prevent obtaining high molar mass PHUs,
J. Appl. Polym. Sci. 2017, 134, 44958-44970
Adrien Cornille, Rémi Auvergne, Oleg Figovsky, Bernard Boutevin and Sylvain Caillol
A perspective approach to sustainable routes for non-isocyanate polyurethanes,
Eur. Polym. J. 2017, 87, 535-552
Adrien Cornille, Marine Blain, Rémi Auvergne, Bruno Andrioletti, Bernard Boutevin and Sylvain Caillol
A study of cyclic carbonate aminolysis at room temperature, effect of cyclic carbonate structures and solvents on polyhydroxyurethane synthesis,
Polym. Chem. 2017, 8, 592-604
Elena Dolci, Vincent Froidevaux, Guillaume Michaud, Frédéric Simon, Rémi Auvergne, Stéphane Fouquay and Sylvain Caillol
Thermoresponsive crosslinked isocyanate-free polyurethanes by Diels-Alder polymerization,
J. Appl. Polym. Sci. 2017, 134, 44408

2016

Elena Dolci, Guillaume Michaud, Frédéric Simon, Stéphane Fouquay, Rémi Auvergne and Sylvain Caillol
Diels-Alder thermoreversible isocyanate-free polyurethanes,
Green Materials 2016, 4, 160-170
Adrien Cornille, Guillaume Michaud, Frederic Simon, Stéphane Fouquay, Rémi Auvergne, Bernard Boutevin and Sylvain Caillol
Promising mechanical and adhesive properties of isocyanate-free poly(hydroxyurethane),
Eur. Polym. J. 2016, 84, 404-420
Marine Blain, Honman Yau, Ludivine Jean-Gérard, Rémi Auvergne, Dominique Benazet, Peter R. Schreiner, Sylvain Caillol and Bruno Andrioletti
Urea- and Thiourea-Catalyzed Aminolysis of Carbonates,
ChemSusChem 2016, 9, 2269-2272
Dolci Elena, Vincent Froidevaux, Christine Joly-Duhamel, Rémi Auvergne, Bernard Boutevin and Sylvain Caillol
Maleimides as a building block for the synthesis of high properties polymers,
Polym. Rev. 2016, 56, 512-556

2015

V. Froideveaux, M. Borne, E. Laborde, R. Auvergne, A. Gandini and B. Boutevin
Study of the Diels–Alder and retro-Diels–Alder reaction between furan derivatives and maleimide for the creation of new materials,
RSC Adv. 2015, 5, 37742-37754
Vincent Froideveaux, Claire Negrell, Elise Laborde, Rémi Auvergne and Bernard Boutevin
Thermosetting material by a thermo responsive cross-linking using retroDiels–Alder and, in situ, Thia-Michael reactions,
Eur. Polym. J. 2015, 69, 510-522
Maxence Fache, Arnaud Viola, Rémi Auvergne, Bernard Boutevin and Sylvain Caillol
Biobased epoxy thermosets from vanillin-derived oligomers,
Eur. Polym. J. 2015, 68, 526-535
Maxence Fache, Rémi Auvergne, Bernard Boutevin and Sylvain Caillol
New vanillin-derived diepoxy monomers for the synthesis of biobased thermosets,
Eur. Polym. J. 2015, 67, 527-538
Audrey Ramone, Audrey Diouf-Lewis, Florence Delor-Jestin, Rémi Auvergne, Sylvain Caillol, Vincent Verney and Fabrice Leroux
Synthesis of Advanced Nanoreinforced Polyurethane with Thiolene Photografted Organo-Modified Layered Double Hydroxide,
Eur. J. Inorg. Chem. 20151203-1211
Emilie Darroman, Lea Bonnot, Rémi Auvergne, Bernard Boutevin and Sylvain Caillol
New aromatic amine based on cardanol giving new biobased epoxy networks with cardanol,
Eur. J. Lipid Sci. Technol. 2015, 117, 178-189

2014

Marine Blain, Ludivine Jean-Gerard, Rémi Auvergne, Dominique Benazet, Sylvain Caillol and Bruno Andrioletti
Rational investigations in the ring opening of cyclic carbonates by amines,
Green Chem. 2014, 16, 4286-4291
Fanny Jaillet, Hélène Nouailhas, Rémi Auvergne, Amédée Ratsimihety, Bernard Boutevin and Sylvain Caillol
Synthesis and characterization of novel vinylester prepolymers from cardanol,
Eur. J. Lipid Sci. Technol. 2014, 116, 928-939
Nicolas Illy, Guillaume Couture, Ghislain David, Rémi Auvergne, Sylvain Caillol and Bernard Boutevin
New prospects for the synthesis of N-alkyl phosphonate/phosphonic acid-bearing oligo-chitosan,
RSC Adv. 2014, 4, 24042-24052
Fatoumata Camara, Sofia Benyahya, Vincent Besse, Gilles Boutevin, Rémi Auvergne, Bernard Boutevin and Sylvain Caillol
Reactivity of secondary amines for the synthesis of non-isocyanate polyurethanes,
Eur. Polym. J. 2014, 55, 17-26
Maxence Fache, Emilie Darroman, Vincent Besse, Rémi Auvergne, Sylvain Caillol and Bernard Boutevin
Vanillin, a promising biobased building-block for monomer synthesis,
Green Chem. 2014, 16, 1987-1998
Myriam Desroches, Sofia Benyahya, Vincent Besse, Rémi Auvergne, Bernard Boutevin and Sylvain Caillol
Synthesis of bio-based building blocks from vegetable oils, A platform chemicals approach,
Lipid Technology 2014, 26, 35-38
Rémi Auvergne, Sylvain Caillol, Ghislain David, Bernard Boutevin and Jean-Pierre Pascault
Biobased Thermosetting Epoxy, Present and Future,
Chem. Rev. 2014, 114, 1082-1115
Nicolas Illy, Sofia Benyahya, Nelly Durand, Rémi Auvergne, Sylvain Caillol, Ghislain David and Bernard Boutevin
The influence of formulation and processing parameters on the thermal properties of a chitosan-epoxy prepolymer system,
Polym. Int. 2014, 63, 420-426
Fanny Jaillet, Emilie Darroman, Amédée Ratsimihety, Rémi Auvergne, Bernard Boutevin and Sylvain Caillol
New biobased epoxy materials from cardanol,
Eur. J. Lipid Sci. Technol. 2014, 116, 63-73
France Millet, Rémi Auvergne, Sylvain Caillol, Ghislain David, Abdelatif Manseri and Nadine Pébère
Improvement of corrosion protection of steel by incorporation of anew phosphonated fatty acid in a phosphorus-containing polymercoating obtained by UV curing,
Prog. Org. Coat. 2014, 77, 285-291
Anne-Laure Brocas, Audrey Llevot, Christos Mantzaridis, Gabriel Cendejas, Rémi Auvergne, Sylvain Caillol, Stéphane Carlotti and Henri Cramail
Epoxidized rosin acids as co-precursors for epoxy resins,
Des. Monomers Polym. 2014, 17, 301-310
Nicolas Illy, Ghislain David, Mike Robitzer, Rémi Auvergne and Sylvain Caillol
Synthesis of Water-Soluble Allyl-Functionalized Oligochitosan and Its Modification by Thiol-Ene Addition in Water,
J. Polym. Sci. Pol. Chem. 2014, 52, 39-48

2013

Christos Mantzaridis, Anne-Laure Brocas, Audrey Llevot, Gabriel Cendejas, Rémi Auvergne, Sylvain Caillol, Stéphane Carlotti and Henri Cramail
Rosin acid oligomers as precursors of DGEBA-free epoxy resins,
Green Chem. 2013, 15, 3091-3098
Vincent Besse, Fatoumata Camara, Coline Voirin, Rémi Auvergne, Sylvain Caillol and Bernard Boutevin
Synthesis and applications of unsaturated cyclocarbonates,
Polym. Chem. 2013, 4, 4545-4561
Vincent Besse, Gabriel Foyer, Rémi Auvergne, Sylvain Caillol and Bernard Boutevin
Access to Nonisocyanate Poly(thio)urethanes, A Comparative Study,
J. Polym. Sci. Pol. Chem. 2013, 51, 3284-3296
Fanny Jaillet, Myriam Desroches, Rémi Auvergne, Bernard Boutevin and Sylvain Caillol
New biobased carboxylic acid hardeners for epoxy resins,
Eur. J. Lipid Sci. Technol. 2013, 115, 698-708
Vincent Besse, Rémi Auvergne, Stéphane Carlotti, Gilles Boutevin, Belkacem Otazaghine, Sylvain Caillol, Jean-Pierre Pascault and Bernard Boutevin
Synthesis of isosorbide based polyurethanes, An isocyanate free method,
React. Funct. Polym. 2013, 73, 588-594
Sylvain Caillol, Myriam Desroches, Stéphane Carlotti, Rémi Auvergne and Bernard Boutevin
Synthesis of new polyurethanes from vegetable oil by thiol-ene coupling,
Green Materials 2013, 1, 16-26

2012

Myriam Desroches, Rémi Auvergne, Bernard Boutevin and Sylvain Caillol
Synthesis of bio-based building blocks from vegetable oils, a platform chemicals approach,
Oilseeds & Craps & Lipids 20121-7
Sylvain Caillol, Myriam Desroches, Gilles Boutevin, Cedric Loubat, Rémi Auvergne and Bernard Boutevin
Synthesis of new polyester polyols from epoxidized vegetable oils and biobased acids,
Eur. J. Lipid Sci. Technol. 2012, 114, 1447-1459
Sofia Benyahya, Jean-Pierre Habas, Rémi Auvergne, Vincent Lapinte and Sylvain Caillol
Structure-property relationships in polyhydroxyurethanes produced from terephthaloyl dicyclocarbonate with various polyamines,
Polym. Int. 2012, 61, 1666-1674
Myriam Desroches, Sylvain Caillol, Stéphane Carlotti, Rémi Auvergne and Bernard Boutevin
Synthèse de polyurethane à partir d'huiles fonctionnalisées par la réaction thiol-ène,
Matériaux & Techniques 20122012
Rémi Auvergne, Myriam Desroches, Sébastien Clerc, Stéphane Carlotti, Sylvain Caillol and Bernard Boutevin
New biobased epoxy hardeners, Thiol-ene addition on oligobutadiene,
React. Funct. Polym. 2012, 72, 393
Ghislain David, Fadéla Iftene, Bernard Boutevin, Rémi Auvergne, A. Alaaeddine and Rachid Meghabar
Novel Dialkyl Vinyl Ether Phosphonate Monomers, Their Synthesis and Alternated Radical Copolymerizations with Electron-Accepting Monomers,
J. Polym. Sci. Pol. Chem. 2012, 50, 2432-2443
Myriam Desroches, Sylvain Caillol, Rémi Auvergne and Bernard Boutevin
Synthesis of pseudo-telechelic diols by transesterification and thiol-ene coupling,
Eur. J. Lipid Sci. Technol. 2012, 114, 84
Myriam Desroches, Maxime Escouvois, Rémi Auvergne, Sylvain Caillol and Bernard Boutevin
From Vegetable Oils to Polyurethanes, Synthetic Routes to Polyols and Main Industrial Products,
Polym. Rev. 2012, 52, 38

2011

Myriam Desroches, Sylvain Caillol, Rémi Auvergne, Bernard Boutevin and Ghislain David
Biobased cross-linked polyurethanes obtained from ester/amide pseudo-diols of fatty acid derivatives synthesized by thiol-ene coupling,
Polym. Chem. 2011, 3, 450
Sofia Benyahya, Myriam Desroches, Rémi Auvergne, Stéphane Carlotti, Sylvain Caillol and Bernard Boutevin
Synthesis of glycerin carbonate-based intermediates using thiol-ene chemistry and isocyanate free polyhydroxyurethanes therefrom,
Polym. Chem. 2011, 2, 2661-2667
Myriam Desroches, Sylvain Caillol, Vincent Lapinte, Rémi Auvergne and Bernard Boutevin
Synthesis of Biobased Polyols by Thiol-Ene Coupling from Vegetable Oils,
Macromolecules 2011, 44, 2489

2010

Rémi Auvergne, Kaewta Kaewtatip, Paul Menut, Varaporn Tanrattanakul, Marie Hélène Morel and Stephane Guilbert
Interactions of Kraft Lignin and Wheat Gluten during Biomaterial Processing, Evidence for the Role of Phenolic Groups,
J. Agric. Food Chem. 2010, 58, 4185

2008

Rémi Auvergne, Marie Hélène Morel, Paul Menut, Olivia Giani, Stephane Guilbert and Jean Jacques Robin
Reactivity of Wheat Gluten Protein during Mechanical Mixing, Radical and Nucleophilic Reactions for the Addition of Molecules on Sulfur,
Biomacromolecules 2008, 9, 664-671

2007

Rémi Auvergne, René Saint-Loup, Christine Joly-Duhamel, Jean-Jacques Robin and Bernard Boutevin
UV curing of a novel resin derived from poly(ethylene terephthalate),
J. Polym. Sci. Pol. Chem. 2007, 45, 1324-1335
Rémi Auvergne, Gael Colomines, Jean Jacques Robin and Bernard Boutevin
Synthesis and Characterization of UV-Curable Resins from the Glycolysis of PET, Vinyl Ether/Maleate UV-Curing System,
Macromol. Chem. Phys. 2007, 208, 690-701

2013

Bernard Boutevin, Rémi Auvergne and Ghislain David
Thiol-ene radical coupling, a powerful technique for the synthesis of polymer precursors, block copolymers and graft copolymers, 217-235
Thiol-X chemistries in Polymer and Materials Science, , 2013.

espaceur 2015

Binders for cork moldings based on polyhydroxyurethanes
S. Caillol, R. Auvergne, B. Boutevin, E. Darroman, C. Balbusquier, C. Loisel
WO2015107113(2015)
Déposé par: DIAM Bouchage, CNRS, ENSCM, UM2
Binders based on epoxy resins for cork molding
S. Caillol, R. Auvergne, B. Boutevin, E. Darroman, C. Balbusquier; C. Loisel
WO2015107114(2015)
Déposé par: DIAM Bouchage, CNRS, ENSCM, UM2

Institut Charles Gerhardt Montpellier - Direction

UMR 5253 - CNRS/UM/ENSCM

Université de Montpellier
Place Eugène Bataillon
CC 1700 - Bâtiment 17 -1er étage
Tel: +33 (0)4 67 14 93 50
Email: direction@icgm.fr

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