Archives pour la catégorie Publications

Poster communication in congresses

[15] I. Miganeh, G. ChatelJournée de printemps de la Société Chimique de France, Chambéry, France, June 15, 2017. Caractérisation d’huiles alimentaires usagées et réduction du taux libres.

[14] A. Makhoufi, T. Cousin, G. Chatel, M. Draye, Journée de printemps de la Société Chimique de France, Chambéry, France, June 15, 2017. Synthèse de Butylphényléther par catalyse par transfert de phase : potentialités des ultrasons.

[13] G. Chatel, C. Monnier, N. Kardos, C. Voiron, B. Andrioletti, M. Draye, Journée de printemps de la Société Chimique de France, Chambéry, France, June 12, 2014. Oxydation verte sélective d’alcools cycliques en cétones.

[12] G. Chatel, E. Naffrechoux, J. Suptil, R. Pflieger, S. Nikitenko, C. Goux-Henry, N. Kardos, B. Andrioletti, M. Draye, Green Chemistry Gordon Conference, Lucca, Italy, July 22–27, 2012. Ionic liquid and ultrasound: A smart combination. To which extent?

[11] C. Monnier, G. Chatel, N. Kardos, C. Goux-Henry, B. Andrioletti, M. Draye, Journée de printemps de la Société Chimique de France, Lyon, France, June 7, 2012. Vers la synthèse verte de l’acide adipique dans les LI.

[10] A. Démolis, G. Chatel, N. Kardos, M. Draye, Journée de printemps de la Société Chimique de France, Lyon, France, June 7, 2012. Mise au point de voies de synthèse de liquides ioniques plus respectueuses de l’environnement.

[9] G. Bal-Fontaine, I. O. Guinea, G. Chatel, N. Kardos, M. Demeunynck, M. Draye, Journée de printemps de la Société Chimique de France, Lyon, France, June 7, 2012. Utilisation de liquides ioniques pour la synthèse de 4-hydroxyiminomethyl-1-alkylpyridinium biologiquement actifs.

[8] G. Chatel, C. Goux-Henry,  N. Kardos, E. Naffrechoux, J. Suptil, B. Andrioletti, M. Draye, 15th Annual Green Chemistry and Engineering Conference & 5th International Conference on Green and Sustainable Chemistry, Washington DC, United States, June 21–23, 2011. Ionic liquid, ultrasound and porphyrin a green combination for olefin epoxidation.

[7] A. Mirabaud, G. Chatel, C. Goux-Henry,  N. Kardos, J. Suptil, B. Andrioletti, M. Draye.. Journée de printemps de la Société Chimique de France, Chambéry, France, June 9, 2011. Ultrasound and ionic liquids: a green combination to alkene epoxidation by a manganese porphyrin.

[6] G. Chatel, M. Draye, B. Andrioletti, N. Kardos, C. Goux-Henry, Green solvents conference, Berchtesgaden, Germany, October 10–13, 2010. Ecofriendly oxidation of olefins catalyzed by transition-metal porphyrins in ionic liquid media.

[5] J. Szymczak, S. Legeai, C. Boulanger, G. Chatel, M. Draye, EUCHEM 2010, 61st Annual Meeting of the International Society of Electrochemistry, Nice, France, September 26–October 1, 2010. Study of bismuth electrochemical system in a piperidinium-based ionic liquid.

[4] G. Chatel, M. Draye, B. Andrioletti, N. Kardos, C. Goux-Henry, Symposium “Tomorrow… Towards a selected chemistry”, Villeurbanne, France, June 3–4, 2010. Oxidation of olefins catalyzed by Mn porphyrins in ionic liquids under ultrasonic activation.

[3] G. Chatel, M. Draye, B. Andrioletti, N. Kardos, C. Goux-Henry, 23ème colloque CBSO2010, Club de Bio-conversion en Synthèse Organique, Royat, France, May 25–28, 2010. Oxydation éco-compatible d’alcènes catalysée par des metallo-porphyrines dans des liquides ioniques à température ambiante.

[2] G. Chatel, M. Draye, B. Andrioletti, N. Kardos, C. Goux-Henry, EUCHEM 2010, Conference on Molten Salts and Ionic Liquids, Bamberg, Germany, March 14–19, 2010. Ecofriendly oxidation of alkenes catalyzed by transition-metal porphyrins in room temperature ionic liquids.

[1] J. Szymczak, S. Legeai, C. Boulanger, G. Chatel, M. Draye, EUCHEM 2010, Conference on Molten Salts and Ionic Liquids, Bamberg, Germany, March 14–19, 2010. Bismuth electrochemistry in a piperidinium-based ionic liquid.

 

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Invited communications and seminars

Invited conferences/seminars:

  • Congrès GePhyX, Grenoble, France, June 6, 2017. Chimie verte et récentes applications en sonochimie pour la valorisation de la biomasse végétale.
  • 250th ACS National Meeting and Exposition, Boston, USA (August 17th, 2015). Investigation of sonochemistry for biomass conversion: That sounds like a good idea!
  • Laboratoire de Chimie Moléculaire et Environnement, Université de Savoie, Chambéry, February 26, 2015. Méthodes d’activation et milieux non-conventionnels pour la valorisation de la biomasse lignocellulosique.

 

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Book chapters

[2] P. N. Amaniampong, R. Behling, N.Araji, S. Valange, K. De Oliveira Vigier, G. Chatel,* In: Green chemistry for sustainable biofuel production [Apple Academic Press], 2017, in press . Sustainable biofuel and chemical production using ionic liquids.

[1] G. Chatel,* In: Sonochemistry: From basic principles to innovative applications [Springer], 2016, 374, 51. Ultrasound in Combination with Ionic Liquids: Studied Applications and Perspectives

 

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Articles in other scientific journal:

Articles published in journals dedicated to scientific community/general public (science popularization):

[15] S. Carenco, C. Oger, G. Chatel, L’Actualité Chimique, March 2017, N°416, 7. Jeunes chimistes de France, qu’attendez-vous du futur réseau international des jeunes chimistes ?

[14] S. Carenco, C. Oger, G. Chatel, Chemistry Views, DOI: 10.1002/chemv.201700007, February 2017. Expectations of Younger Chemists in France.

[13] C. Oger, G. Chatel, L’Actualité Chimique, January 2017, N°414, 8–9. Le RJ-SCF en 2017 : Vers la fin d’un mandat et (peut-être) de nouveaux projets…

[12] A. Wannebroucq, G. Chatel, L’Actualité Chimique, October 2016, N°411, 7–9. Quel emploi pour les jeunes chimistes ?

[11] D. Chambre, G. Chatel, L’Actualité Chimique, September 2016, N°410, 45–49. Comment utiliser les ultrasons au laboratoire ? Exemples et prise en main.

[10] R. Behling, N. Araji, G. Chatel, L’Actualité Chimique, September 2016, N°410, 11–20. Qu’est-ce que la sonochimie ?

[9] G. Chatel, L’Actualité Chimique, September 2016, N°410, 9–10. La sonochimie ou comment les ultrasons font vibrer la chimie ! Avant-propos

[8] C. Oger, G. Chatel, Chemistry Views, DOI: 10.1002/chemv.201600051, July 2016. French Young Chemists’ Network: Two Years Already!

[7] C. Oger, G. Chatel, L’Actualité Chimique, June-July 2016, N°408-409, 8–10. Réseau des jeunes chimistes de la SCF : deux ans déjà !

[6] M. Rossato, G. Chatel, L’Actualité Chimique, March 2016, N°405, 6–9. Qu’attendent les jeunes chimistes de la SCF ?

[5] C. Addamiano, G. Chatel, L’Actualité Chimique, December 2015, N°402, 6–7. Pourquoi adhérer à la Société Chimique de France ?

[4] M. Rossato, G. Chatel, L’Actualité Chimique, October-November 2015, N°400-401, 8–9. Que pensent-ils donc de L’Actualité Chimique ?

[3] C. Oger, G. Chatel, L’Actualité Chimique, June-July 2015, N°397-398, 7. D’une visibilité nationale vers une visibilité internationale.

[2] C. Oger, G. Chatel, Chemistry Views, DOI: 10.1002/chemv.201400139, June 2015. French Young Chemists’ Network Created.

[1] G. Chatel, L’Actualité Chimique, April 2015, N°395, 4. Un nouveau réseau… une nouvelle rubrique !

 

 

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Academic theses:

Academic Theses:

[1] G. Chatel, Master’s Internship (1st year), 2008 Université de Savoie, Laboratoire de Chimie Moléculaire et Environnment (LCME), France Thesis Title: One-pot syntheses of ionic liquidsAdvisor: Prof. Micheline DRAYEThesis pdf available here (in French)

[2] G. Chatel, Master’s Internship (2nd year), 2009 Université Laval, Département de Chimie, Canada Thesis Title: New catalytic methods in green chemistry Advisor: Prof. Thierry OLLEVIER Thesis pdf available here (in French)

[3] G. Chatel, PhD in Chemistry, 2012 Université de Savoie, Laboratoire de Chimie Moléculaire et Environnement (LCME) and Université Claude Bernard Lyon 1, Laboratoire de Catalyse, Synthèse et Environnement, France Thesis Title: Ionic liquids and ultrasound assisted epoxidation: a green and synergic combination Advisors: Prof. Micheline DRAYE and Prof. Bruno ANDRIOLETTI Thesis pdf available here (in French)

 

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2017 2016 2015 2014 2013 2012

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Articles published in 2012

2012

[5] G. Chatel, L. Leclerc, E. Naffrechoux, C. Bas, N. Kardos, C. Goux-Henry, B. Andrioletti, M. Draye, J. Chem. Eng. Data 2012, 57, 3385−3390. Ultrasonic properties of hydrophobic bis(trifluoromethylsulfonyl)imide-based ionic liquids. http://pubs.acs.org/doi/abs/10.1021/je300377a

[4] J. Szymczak, S. Legeai, S. Diliberto, S. Migot, N. Stein, C. Boulanger, G. Chatel, M. Draye, Electrochem. Commun. 2012, 24, 57–60. Template-free electrodeposition of tellurium nanostructures in a room-temperature ionic liquid. http://www.sciencedirect.com/science/article/pii/S138824811200344X

[3] G. Chatel, C. Goux-Henry, A. Mirabaud, T. Rossi, N. Kardos, B. Andrioletti, M. Draye, J. Catal. 2012, 291, 127–132. H2O2/NaHCO3 mediated enantioselective epoxidation of olefins in NTf2 based ionic liquids and under ultrasound. http://www.sciencedirect.com/science/article/pii/S002195171200125X

[2] S. Viboud, N. Papaiconomou, A. Cortesi, G. Chatel, M. Draye, D. Fontvieille, J. Hazard. Mat. 2012, 215216, 40–48. Correlating the structure and composition of ionic liquids with their toxicity on Vibrio fischeri: a systematic study. http://www.sciencedirect.com/science/article/pii/S0304389412001653

[1] G. Chatel, C. Goux-Henry, N. Kardos, J. Suptil, B. Andrioletti, M. Draye, Ultrason. Sonochem.  2012, 19, 390–394. Ultrasound and ionic liquid: an efficient combination to tune the mechanism of alkenes epoxidation. http://www.sciencedirect.com/science/article/pii/S1350417711002100 

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Articles published in 2013

2013

[6] G. Chatel,R. Pflieger, E. Naffrechoux, S. I. Nikitenko, J. Suptil, C. Goux-Henry, N. Kardos, B. Andrioletti, M. Draye, ACS Sustain. Chem. Eng.  2013, 1, 137–143. Hydrophobic bis(trifluoromethylsulfonyl)imide based ionic liquids pyrolysis: through the window of the ultrasonic reactor. http://pubs.acs.org/doi/abs/10.1021/sc300068d

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Articles published in 2014

2014

[14] D. Rinsant, G. Chatel,* F. Jérôme, ChemCatChem 2014, 6, 3355–3359. Efficient and selective oxidation of D-glucose into gluconic acid under low frequency ultrasonic irradiation http://onlinelibrary.wiley.com/doi/10.1002/cctc.201402604/abstract  

[13] G. Chatel,* D. R. MacFarlane, Chem. Sov. Rev. 2014, 43, 8132–8149. Ionic liquids and ultrasound in combination: synergies and challenges http://pubs.rsc.org/en/Content/ArticleLanding/2014/CS/C4CS00193A

[12] G. Chatel,* K. De Oliveira Vigier, F. Jérôme, ChemSusChem 2014, 7, 2774–2787. Sonochemistry: what potential for conversion of lignocellulosic biomass into platform chemicals?http://onlinelibrary.wiley.com/doi/10.1002/cssc.201402289/abstract

[11] F. Cheng, H. Wang, G. Chatel, G. Gurau, R. D. Rogers, Bioresour. Technol. 2014, 164,394–401. Facile pulping of lignocellulosic biomass using choline acetate. http://www.sciencedirect.com/science/article/pii/S0960852414006750

[10] P. D. McCrary, G. Chatel, S. A. Alaniz, O. A. Cojocaru, P. A. Beasley, L. A. Flores, S. P. Kelley, P. S. Barber, R. D. Rogers, Energy Fuels 2014, 28, 3460–3473. Evaluating ionic liquids as hypergolic fuels: Exploring reactivity from molecular structure. http://pubs.acs.org/doi/abs/10.1021/ef500264z

[9] G. Chatel, C. Monnier, C. Voiron, N. Kardos,  B. Andrioletti, M. Draye, Appl. Catal. A 2014, 478, 157–164. Green, selective and swift oxidation of cyclic alcohols to corresponding ketones. http://www.sciencedirect.com/science/article/pii/S0926860X14001860

[8] G. Chatel, J. F. B. Pereira, V. Debbeti, H. Wang, R. D. Rogers, Green Chem. 2014, 16, 2051–2083. Mixing ionic liquids – “simple mixtures” or “double salts”? (Article of themed collection: “15 Years of Green Chemistry”) http://pubs.rsc.org/en/content/articlelanding/2014/gc/c3gc41389f Pdf available – Open Access : here

[7] G. Chatel, R. D. Rogers, ACS Sustainable Chem. Eng. 2014, 2, 322–339. Review: Oxidation of lignin using ionic liquids – An innovative strategy to produce renewable chemicals. (Selected as the cover of the journal, March 2014)                           http://pubs.acs.org/doi/abs/10.1021/sc4004086

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Articles published in 2015

2015

[16] K. De Oliveira Vigier, G. Chatel,  F. Jérôme, ChemCatChem 2015, 7, 1250–1260. Contribution of deep eutectic solvents for biomass processing: opportunities, challenges, and limitations. http://onlinelibrary.wiley.com/wol1/doi/10.1002/cctc.201500134/abstract

[15] H. Wang, S. P. Kelley, J. W. Brantley III, G. Chatel, J. Shamshina, J. F. B. Pereira, V. Debbeti, A. S. Myerson, R. D. Rogers, ChemPhysChem 2015, 16, 993–1002. Ionic fluids containing both strongly and weakly interacting ions of the same charge have unique ionic and chemical environments as a function of ion concentration. http://onlinelibrary.wiley.com/doi/10.1002/cphc.201402894/abstract

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