Laboratoire des Interactions Moléculaires et Réactivité Chimique et Photochimique
UMR 5623


Scientific production

Publications

Xanthate-mediated synthesis of functional bis(γ-thiolactones)
Tetrahedron Letters, 2019, 60, 1522-1525
Langlais, M.; Coutelier, O.; Destarac, M.
DOI: 10.1016/j.tetlet.2019.05.004
CE/LIF from apogee to slow cruising speed, for a nice future.
Chromatography Today, 2019, 12, 28-33
Couderc, F.; Gavard, P.; Gavard, A.; Ong-Meang, V.
DOI:

1-Ethyl-3-methylimidazolium tartrate chiral ionic liquids: preparation, characterization and opportunities thereof.
New J. Chem., 2018, 42, 18739-18748
Castellan, T.; Cuyamendous, C.; Fitremann, J.; Galano, J.M.; Oger, C.; Durand, T.; Guillen, F.; Génisson, Y.
DOI: 10.1039/C8NJ03175D

Quench ionic flash nano precipitation as a simple and tunable approach to decouple growth and functionalization for the one-step synthesis of functional LnPO4 -based nanoparticles in water
Chem. Commun., 2018, 54, 9438-9441
Pinkerton, N.M.; Hadri, K.; Amouroux, B.; Behar, L.; Mingotaud, C.; Destarac, M.; Kulai, I.; Mazières, S.; Chassaing, S.; Marty, J.D.
DOI: 10.1039/C8CC04163F

Scope and limitations of ring-opening copolymerization of trimethylene carbonate with substituted γ-thiolactones.
Polym. Chem., 2018, 9, 2769-2774
Langlais, M.; Coutelier, O.; Moins, S.; De Winter, J.; Coulembier, O.; Destarac, M.
DOI: 10.1039/C8PY00127H

Scope and Limitations of Xanthate-Mediated Synthesis of Functional γ-Thiolactones
ACS Omega, 2018, 3, 17732-17742
Langlais, M.; Coutelier, O.; Destarac, M.
DOI: 10.1021/acsomega.8b02962

Simple electron donor molecules based on triphenylamine and carbazole derivatives.
Dyes Pigm., 2018, 153, 275-283
Bélières, M.; Sartor, V.; Fabre, P.L.; Poteau, R.; Bordeau, G.; Chouini-Lalanne, N.
DOI: 10.1016/j.dyepig.2018.02.022

Simple Synthetic Molecular Hydrogels from Self-Assembling Alkylgalactonamides as Scaffold for 3D Neuronal Cell Growth.
ACS Appl. Mater. Interfaces, 2018, 10, 17004-17017
Chalard, A.; Vaysse, L.; Joseph, P.; Malaquin, L.; Souleille, S.; Lonetti, B.; Sol, J.C.; Loubinoux, I.; Fitremann, J.
DOI: 10.1021/acsami.8b01365

The Chain Length Distribution of an Ideal Reversible Deactivation Radical Polymerization.
Polymers, 2018, 10, 887 (1 à 9)
Harrisson, S.
DOI: 10.3390/polym10080887

The downside of dispersity: why the standard deviation is a better measure of dispersion in precision polymerization.
Polym. Chem., 2018, 9, 1366-1370
Harrisson, S.
DOI: 10.1039/C8PY00138C

Thiolactone-Functional Reversible Deactivation Radical Polymerization Agents for Advanced Macromolecular Engineering.
Macromolecules, 2018, 51, 4315-4324
Langlais, M.; Coutelier, O.; Destarac, M.
DOI: 10.1021/acs.macromol.8b00770

Three-dimensional directionality is a pivotal structural feature for the bioactivity of Azabisphosphonate-capped poly(PhosphorHydrazone) nanodrug dendrimers.
Biomacromolecules, 2018, 19, 712-720
Hayder, M.; Garzoni, M.; Bochicchio, D.; Caminade, A.M.; Couderc, F.; Ong-Meang, V.; Davignon, J.L.; Turrin, C.O.; Pavan, G.M.; Poupot, R.
DOI: 10.1021/acs.biomac.7b01398

ω-Methylsulfanylalkyl Glucosinolates: A General Synthetic Pathway.
Molecules, 2018, 23, 786-800
Mavratzotis, M.; Cassel, S.; Montaut, S.; Rollin, P.
DOI: 10.3390/molecules23040786

A quantification of the Soai reaction.
ChemCatChem, 2018, 10, 642-648
Noble-Terán, M.E.; Cruz, J.M.; Micheau, J.C.; Buhse, T.
DOI: 10.1002/cctc.201701554

Anticyclonic eddies increase accumulation of microplastic in the North Atlantic subtropical gyre.
Mar. Pollut. Bull., 2018, 126, 191-196
Brach, L.; Deixonne, P.; Bernard, M.F.; Durand, E.; Desjean, M.C.; Perez, E.; van Sebille, E.; Halle, T.
DOI: 10.1016/j.marpolbul.2017.10.077

Asymmetric Copolymers: Synthesis, Properties, and Applications of Gradient and Other Partially Segregated Copolymers.
Macromol. Rapid Commun., 2018, 39, 1800357(1 à 22)
Zhang, J.; Farias-Mancilla, B.; Destarac, M.; Schubert, U.S.; Keddie, D.J.; Guerrero-Sanchez, C.; Harrisson, S.
DOI: 10.1002/marc.201800357

Current opinion: What is a nanoplastic?.
Environ. Pollut., 2018, 235, 1030-1034
Gigault, J.; Halle, T.; Baudrimont, M.; Pascal, P.Y.; Gauffre, F.; Phi, T.L.; Hadri, H.El; Grassl, B.; Reynaud, S.
DOI: 10.1016/j.envpol.2018.01.024

Extended photo-induced endosome-like structures in giant vesicles promoted by block-copolymer nanocarriers.
Nanoscale, 2018, 10, 15442-15446
Montis, C.; Till, U.; Vicendo, P.; Roux, C.; Mingotaud, A.F.; Violleau, F.; Demazeau, M.; Berti, D.; Lonetti, B.
DOI: 10.1039/C8NR04355H

Hyaluronan based materials with catanionic sugar-derived surfactants as drug delivery systems.
Colloids Surf. B Biointerfaces, 2018, 164, 218-223
Roig, F.; Blanzat, M.; Solans, C.; Esquena, J.; García-Celma, M.J.
DOI: 10.1016/j.colsurfb.2018.01.037

Hybrid vesicles from lipids and block copolymers: Phase behavior from the micro- to the nano-scale.
Colloids Surf. B Biointerfaces, 2018, 168, 18-28
Magnani, C.; Montis, C.; Mangiapia, G.; Mingotaud, A.F.; Mingotaud, C.; Roux, C.; Joseph, P.; Berti, D.; Lonetti, B.
DOI: 10.1016/j.colsurfb.2018.01.042

Impact of polyacrylamide adsorption on flow through porous siliceous materials: State of the art, discussion and industrial concern.
J. Colloid Interf. Sci., 2018, 531, 693-704
Bessaies-Bey, H.; Fusier, J.; Harrisson, S.; Destarac, M.; Jouenne, S.; Passade-Boupat, N.; Lequeux, F.; de Lacaillerie, J.B. d'Espi; Sanson, N.
DOI: 10.1016/j.jcis.2018.07.103

Industrial development of reversible-deactivation radical polymerization : is the induction period over?
Polym. Chem., 2018, 9, 4947-4967
Destarac, M.
DOI: 10.1039/C8PY00970H

Influence of dermal formulation additives on the physicochemical characteristics of catanionic vesicles
Colloids Surf. A Physicochem. Eng., 2018, 558, 373-383
Richard, C.; Souloumiac, E.; Jestin, J.; Blanzat, M.; Cassel, S.
DOI: 10.1016/j.colsurfa.2018.09.007

Influence of sodium dodecyl sulfate on the kinetics and control of RAFT/MADIX polymerization of acrylamide.
J. Polym. Sci. Part A: Polym. Chem., 2018, 56, 760-765
Barthet, C.; Wilson, J.; Cadix, A.; Destarac, M.; Chassenieux, C.; Harrisson, S.
DOI: 10.1002/pola.28949

Interfacial activity and emulsifying behaviour of inclusion complexes between helical polysaccharides and flavouring molecules resulting from non-covalent interactions.
Food Res. Int., 2018, 105, 801-811
De Fenoyl, L.; Hirel, D.; Perez, E.; Lecomte, S.; Morvan, E.; Delample, M.
DOI: 10.1016/j.foodres.2017.11.064

Kinetic and copolymer composition investigations of the free radical copolymerization of 1-Octene with Glycidyl Methacrylate.
Macromol. Chem. Phys., 2018, 219, 1800084
Rosales‐Guzmán, M.; Pérez‐Camacho, O.; Torres‐Lubián, R.; Harrisson, S.; Schubert, U.S.; Guerrero‐Sánchez, C.; Saldívar‐Guerra, E.
DOI: 10.1002/macp.201800084

Marangoni-driven flower-like patterning of an evaporating drop spreading on a liquid substrate.
Nat. Commun., 2018, 9, 1-12
Wodlei, F.; Sebilleau, J.; Magnaudet, J.; Pimienta, V.
DOI: 10.1038/s41467-018-03201-3

Mechanistic Insights into Polyion Complex Associations.
Macromolecules, 2018, 51, 1427-1440
Gineste, S.; Di Cola, E.; Amouroux, B.; Till, U.; Marty, J.D.; Mingotaud, A.F.; Mingotaud, C.; Violleau, F.; Berti, D.; Parigi, G.; Luchinat, C.; Balor, S.; Sztucki, M.; Lonetti, B.
DOI: 10.1021/acs.macromol.7b02391

Mixing Time between Organometallic Precursor and Ligand: A Key Parameter Controlling ZnO Nanoparticle Size and Shape and Processable Hybrid Materials.
Chem. Mater., 2018, 30, 8959-8967
Zhao, Z.; Coppel, Y.; Fitremann, J.; Fau, P.; Roux, C.; Lepetit, C.; Lecante, P.; Marty, J.D.; Mingotaud, C.; Kahn, M.L.
DOI: 10.1021/acs.chemmater.8b04480
Nonspecific symbiosis between sophora flavescens and different rhizobia.
Mol. Plant-Microbe Interact., 2018, 31, 224-232
Liu, Y.Hui; Jiao, Y.Shan; Liu, L.Xue; Wang, D.; Tian, C.Fu; Wang, E.Tao; Wang, L.; Chen, W.Xin; Wu, S.Ying; Guo, B.Lin; Guan, Z.Gen; Poinsot, V.; Chen, W.Feng
DOI: 10.1094/MPMI-05-17-0117-R

Pages

2023 IMRCP