Cation−Anion−CO2 Interactions in Imidazolium-Based Ionic Liquid Sorbents

Autor: Hubert Stassen, Graciane Marin, Jairton Dupont, Anne-Lise Girard, Marcileia Zanatta, Jessé Neumann, Nathalia M. Simon

Publikováno v: ChemPhysChem. 19:2879-2884

A series of functionalized N-alkylimidazolium based ionic liquids (ImILs) were designed, through anion (carboxylates and halogenated) and cation (N-alkyl side chains) structural modifications, and studied as potential sorbents for CO2 . The sorption

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::72c96d8403170d20bcc499059216f850
https://doi.org/10.1002/cphc.201800751

Cation-Anion-CO

Autor: Nathalia M, Simon, Marcileia, Zanatta, Jessé, Neumann, Anne-Lise, Girard, Graciane, Marin, Hubert, Stassen, Jairton, Dupont

Publikováno v: Chemphyschem : a European journal of chemical physics and physical chemistry. 19(21)

A series of functionalized N-alkylimidazolium based ionic liquids (ImILs) were designed, through anion (carboxylates and halogenated) and cation (N-alkyl side chains) structural modifications, and studied as potential sorbents for CO

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3fdb37a60927a731b46f9c42a04835d2
https://pubmed.ncbi.nlm.nih.gov/30092119

Insights on recyclable catalytic system composed of task-specific ionic liquids for the chemical fixation of carbon dioxide

Autor: Anne-Lise Girard, Sandro Marmitt, Jairton Dupont, Paulo Fernando Bruno Gonçalves, Marcileia Zanatta, Nathalia M. Simon

Publikováno v: Green Chem.. 16:2815-2825

A series of imidazolium-based ionic liquids (ILs) were synthesised and used as single component and metal-free homogeneous catalysts to convert a renewable, inexpensive and non-toxic CO2 feedstock into useful products. The cycloaddition of carbon dio

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::de20ff8da3ef7d0e35c8a837ebf1f947
https://doi.org/10.1039/c4gc00127c

Influence of the Acetylenic Substituent on the Intramolecular Carbolithiation of Alkynes

Autor: Muriel Durandetti, Anne-Lise Girard, Rudy Lhermet, Catherine Fressigné, Jacques Maddaluno

Publikováno v: European Journal of Organic Chemistry
European Journal of Organic Chemistry, 2012, 2012 (15), pp.2895-2905. ⟨10.1002/ejoc.201101777⟩
European Journal of Organic Chemistry, Wiley-VCH Verlag, 2012, 2012 (15), pp.2895-2905. ⟨10.1002/ejoc.201101777⟩

The intramolecular carbolithiation of a series of propargylic ethers has been performed to evaluate the influence of the terminal substituent on the efficiency and the stereochemical outcome of the cyclization. Our results show that only 5-exo-dig cy

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d200d538be11a4e09fde9d96194fb30f
https://doi.org/10.1002/ejoc.201101777

Influence of the acetylenic substituent on the intramolecular carbolithiation of alkynes: a DFT theoretical study

Autor: Rudy Lhermet, Catherine Fressigné, Jacques Maddaluno, Muriel Durandetti, Anne-Lise Girard

Publikováno v: Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2013, 78 (19), pp.9659-9669. ⟨10.1021/jo4012893⟩

International audience; A theoretical study of the intramolecular 5-exo-dig carbolithiation of substituted propargyl o-lithioaryl ethers, leading to dihydrobenzofurans, has been performed. The results show that a DFT description of the reaction (B3P8

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69bcbe00aeb081dc429986d2e7ffa5d2
https://hal.archives-ouvertes.fr/hal-00992025