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Insights into the mechanism of extraction of uranium (VI) from nitric acid solution into an ionic liquid by using tri-n-butyl phosphate.

Chemphyschem : a European journal of chemical physics and physical chemistry

Gaillard DC, Boltoeva M, Billard I, Georg S, Mazan V, Ouadi A, Ternova D, Hennig C.
PMID: 26149535
Chemphyschem. 2015 Aug 24;16(12):2653-62. doi: 10.1002/cphc.201500283. Epub 2015 Jul 06.

We present new results on the liquid-liquid extraction of uranium (VI) from a nitric acid aqueous phase into a tri-n-butyl phosphate/1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (TBP/[C4 mim][Tf2 N]) phase. The individual solubilities of the ionic-liquid ions in the upper part of the...

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Gaillard DC, Boltoeva M, Billard I, et al. Insights into the mechanism of extraction of uranium (VI) from nitric acid solution into an ionic liquid by using tri-n-butyl phosphate. Chemphyschem. 2015;16(12):2653-62doi: 10.1002/cphc.201500283.
Gaillard, D. C., Boltoeva, M., Billard, I., Georg, S., Mazan, V., Ouadi, A., Ternova, D., & Hennig, C. (2015). Insights into the mechanism of extraction of uranium (VI) from nitric acid solution into an ionic liquid by using tri-n-butyl phosphate. Chemphyschem : a European journal of chemical physics and physical chemistry, 16(12), 2653-62. https://doi.org/10.1002/cphc.201500283
Gaillard, Dr Clotilde, et al. "Insights into the mechanism of extraction of uranium (VI) from nitric acid solution into an ionic liquid by using tri-n-butyl phosphate." Chemphyschem : a European journal of chemical physics and physical chemistry vol. 16,12 (2015): 2653-62. doi: https://doi.org/10.1002/cphc.201500283
Gaillard DC, Boltoeva M, Billard I, Georg S, Mazan V, Ouadi A, Ternova D, Hennig C. Insights into the mechanism of extraction of uranium (VI) from nitric acid solution into an ionic liquid by using tri-n-butyl phosphate. Chemphyschem. 2015 Aug 24;16(12):2653-62. doi: 10.1002/cphc.201500283. Epub 2015 Jul 06. PMID: 26149535.
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Copper-Catalyzed Perfluoroalkylthiolation of Alkynes with Perfluoroalkanesulfenamides.

Chemistry (Weinheim an der Bergstrasse, Germany)

Tlili A, Alazet S, Glenadel Q, Billard T.
PMID: 27334703
Chemistry. 2016 Jul 11;22(29):10230-4. doi: 10.1002/chem.201601338. Epub 2016 Jun 23.

Copper-catalyzed direct perfluoroalkylthiolation of alkynes by using the corresponding perfluoroalkanesulfenamide reagent is reported. The selective mono- and bis-perfluoroalkylthiolation of alkynes can be conducted under very mild conditions (no base, room temperature) in very good to excellent yields. This approach,...

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Tlili A, Alazet S, Glenadel Q, et al. Copper-Catalyzed Perfluoroalkylthiolation of Alkynes with Perfluoroalkanesulfenamides. Chemistry. 2016;22(29):10230-4doi: 10.1002/chem.201601338.
Tlili, A., Alazet, S., Glenadel, Q., & Billard, T. (2016). Copper-Catalyzed Perfluoroalkylthiolation of Alkynes with Perfluoroalkanesulfenamides. Chemistry (Weinheim an der Bergstrasse, Germany), 22(29), 10230-4. https://doi.org/10.1002/chem.201601338
Tlili, Anis, et al. "Copper-Catalyzed Perfluoroalkylthiolation of Alkynes with Perfluoroalkanesulfenamides." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 22,29 (2016): 10230-4. doi: https://doi.org/10.1002/chem.201601338
Tlili A, Alazet S, Glenadel Q, Billard T. Copper-Catalyzed Perfluoroalkylthiolation of Alkynes with Perfluoroalkanesulfenamides. Chemistry. 2016 Jul 11;22(29):10230-4. doi: 10.1002/chem.201601338. Epub 2016 Jun 23. PMID: 27334703.
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Polarization shaping for unidirectional rotational motion of molecules.

Physical review letters

Karras G, Ndong M, Hertz E, Sugny D, Billard F, Lavorel B, Faucher O.
PMID: 25815926
Phys Rev Lett. 2015 Mar 13;114(10):103001. doi: 10.1103/PhysRevLett.114.103001. Epub 2015 Mar 10.

Control of the orientation of the angular momentum of linear molecules is demonstrated by means of laser polarization shaping. For this purpose, we combine two orthogonally polarized and partially time-overlapped femtosecond laser pulses so as to produce a spinning...

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Karras G, Ndong M, Hertz E, et al. Polarization shaping for unidirectional rotational motion of molecules. Phys Rev Lett. 2015;114(10):103001doi: 10.1103/PhysRevLett.114.103001.
Karras, G., Ndong, M., Hertz, E., Sugny, D., Billard, F., Lavorel, B., & Faucher, O. (2015). Polarization shaping for unidirectional rotational motion of molecules. Physical review letters, 114(10), 103001. https://doi.org/10.1103/PhysRevLett.114.103001
Karras, G, et al. "Polarization shaping for unidirectional rotational motion of molecules." Physical review letters vol. 114,10 (2015): 103001. doi: https://doi.org/10.1103/PhysRevLett.114.103001
Karras G, Ndong M, Hertz E, Sugny D, Billard F, Lavorel B, Faucher O. Polarization shaping for unidirectional rotational motion of molecules. Phys Rev Lett. 2015 Mar 13;114(10):103001. doi: 10.1103/PhysRevLett.114.103001. Epub 2015 Mar 10. PMID: 25815926.
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Synthetic Approaches to Trifluoromethylselenolated Compounds.

Chemistry (Weinheim an der Bergstrasse, Germany)

Tlili A, Ismalaj E, Glenadel Q, Ghiazza C, Billard T.
PMID: 29072337
Chemistry. 2018 Mar 12;24(15):3659-3670. doi: 10.1002/chem.201704637. Epub 2017 Dec 12.

The association of trifluoromethyl group to chalcogens gives new fluorinated substituents with specific properties, mainly in term of lipophilicity. The trifluoromethylselenyl group is the last of the series that has been studied and despite pioneering approaches in the late...

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Tlili A, Ismalaj E, Glenadel Q, et al. Synthetic Approaches to Trifluoromethylselenolated Compounds. Chemistry. 2017;24(15):3659-3670doi: 10.1002/chem.201704637.
Tlili, A., Ismalaj, E., Glenadel, Q., Ghiazza, C., & Billard, T. (2018). Synthetic Approaches to Trifluoromethylselenolated Compounds. Chemistry (Weinheim an der Bergstrasse, Germany), 24(15), 3659-3670. https://doi.org/10.1002/chem.201704637
Tlili, Anis, et al. "Synthetic Approaches to Trifluoromethylselenolated Compounds." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 24,15 (2018): 3659-3670. doi: https://doi.org/10.1002/chem.201704637
Tlili A, Ismalaj E, Glenadel Q, Ghiazza C, Billard T. Synthetic Approaches to Trifluoromethylselenolated Compounds. Chemistry. 2018 Mar 12;24(15):3659-3670. doi: 10.1002/chem.201704637. Epub 2017 Dec 12. PMID: 29072337.
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Siderophore-Mediated Iron Dissolution from Nontronites Is Controlled by Mineral Cristallochemistry.

Frontiers in microbiology

Parrello D, Zegeye A, Mustin C, Billard P.
PMID: 27064911
Front Microbiol. 2016 Mar 31;7:423. doi: 10.3389/fmicb.2016.00423. eCollection 2016.

Bacteria living in oxic environments experience iron deficiency due to limited solubility and slow dissolution kinetics of iron-bearing minerals. To cope with iron deprivation, aerobic bacteria have evolved various strategies, including release of siderophores or other organic acids that...

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Parrello D, Zegeye A, Mustin C, et al. Siderophore-Mediated Iron Dissolution from Nontronites Is Controlled by Mineral Cristallochemistry. Front Microbiol. 2016;7:423doi: 10.3389/fmicb.2016.00423.
Parrello, D., Zegeye, A., Mustin, C., & Billard, P. (2016). Siderophore-Mediated Iron Dissolution from Nontronites Is Controlled by Mineral Cristallochemistry. Frontiers in microbiology, 7423. https://doi.org/10.3389/fmicb.2016.00423
Parrello, Damien, et al. "Siderophore-Mediated Iron Dissolution from Nontronites Is Controlled by Mineral Cristallochemistry." Frontiers in microbiology vol. 7 (2016): 423. doi: https://doi.org/10.3389/fmicb.2016.00423
Parrello D, Zegeye A, Mustin C, Billard P. Siderophore-Mediated Iron Dissolution from Nontronites Is Controlled by Mineral Cristallochemistry. Front Microbiol. 2016 Mar 31;7:423. doi: 10.3389/fmicb.2016.00423. eCollection 2016. PMID: 27064911; PMCID: PMC4814481.
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Gentle Nearest Neighbors Boosting over Proper Scoring Rules.

IEEE transactions on pattern analysis and machine intelligence

Nock R, Ali WB, D'Ambrosio R, Nielsen F, Barlaud M.
PMID: 26353210
IEEE Trans Pattern Anal Mach Intell. 2015 Jan;37(1):80-93. doi: 10.1109/TPAMI.2014.2307877.

Tailoring nearest neighbors algorithms to boosting is an important problem. Recent papers study an approach, UNN, which provably minimizes particular convex surrogates under weak assumptions. However, numerical issues make it necessary to experimentally tweak parts of the UNN algorithm,...

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Nock R, Ali WB, D'Ambrosio R, et al. Gentle Nearest Neighbors Boosting over Proper Scoring Rules. IEEE Trans Pattern Anal Mach Intell. 2015;37(1):80-93doi: 10.1109/TPAMI.2014.2307877.
Nock, R., Ali, W. B., D'Ambrosio, R., Nielsen, F., & Barlaud, M. (2015). Gentle Nearest Neighbors Boosting over Proper Scoring Rules. IEEE transactions on pattern analysis and machine intelligence, 37(1), 80-93. https://doi.org/10.1109/TPAMI.2014.2307877
Nock, Richard, et al. "Gentle Nearest Neighbors Boosting over Proper Scoring Rules." IEEE transactions on pattern analysis and machine intelligence vol. 37,1 (2015): 80-93. doi: https://doi.org/10.1109/TPAMI.2014.2307877
Nock R, Ali WB, D'Ambrosio R, Nielsen F, Barlaud M. Gentle Nearest Neighbors Boosting over Proper Scoring Rules. IEEE Trans Pattern Anal Mach Intell. 2015 Jan;37(1):80-93. doi: 10.1109/TPAMI.2014.2307877. PMID: 26353210.
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Biology of the gametes of some teleost species.

Fish physiology and biochemistry

Billard R, Christen R, Cosson MP, Gatty JL, Letellier L, Renard P, Saad A.
PMID: 24233173
Fish Physiol Biochem. 1986 Oct;2(1):115-20. doi: 10.1007/BF02264079.

Our knowledge of the biology of fish gametes is still limited. Up to now research was short-term, aiming at solving practical questions connected with gamete storage and artificial insemination. More information on gamete biology is now available and has...

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Billard R, Christen R, Cosson MP, et al. Biology of the gametes of some teleost species. Fish Physiol Biochem. 1986;2(1):115-20doi: 10.1007/BF02264079.
Billard, R., Christen, R., Cosson, M. P., Gatty, J. L., Letellier, L., Renard, P., & Saad, A. (1986). Biology of the gametes of some teleost species. Fish physiology and biochemistry, 2(1), 115-20. https://doi.org/10.1007/BF02264079
Billard, R, et al. "Biology of the gametes of some teleost species." Fish physiology and biochemistry vol. 2,1 (1986): 115-20. doi: https://doi.org/10.1007/BF02264079
Billard R, Christen R, Cosson MP, Gatty JL, Letellier L, Renard P, Saad A. Biology of the gametes of some teleost species. Fish Physiol Biochem. 1986 Oct;2(1):115-20. doi: 10.1007/BF02264079. PMID: 24233173.
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Correction to "assessing the dual activity of a chalcone-phthalocyanine conjugate: design, synthesis, and antivascular and photodynamic properties".

Molecular pharmaceutics

Tuncel S, Trivella A, Atilla D, Bennis K, Savoie H, Albrieux F, Delort L, Billard H, Dubois V, Ahsen V, Caldefie-Chézet F, Richard C, Boyle RW, Ducki S, Dumoulin F.
PMID: 25590168
Mol Pharm. 2015 Feb 02;12(2):663. doi: 10.1021/mp5008426. Epub 2015 Jan 15.

No abstract available.

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Tuncel S, Trivella A, Atilla D, et al. Correction to "assessing the dual activity of a chalcone-phthalocyanine conjugate: design, synthesis, and antivascular and photodynamic properties". Mol Pharm. 2015;12(2):663doi: 10.1021/mp5008426.
Tuncel, S., Trivella, A., Atilla, D., Bennis, K., Savoie, H., Albrieux, F., Delort, L., Billard, H., Dubois, V., Ahsen, V., Caldefie-Chézet, F., Richard, C., Boyle, R. W., Ducki, S., & Dumoulin, F. (2015). Correction to "assessing the dual activity of a chalcone-phthalocyanine conjugate: design, synthesis, and antivascular and photodynamic properties". Molecular pharmaceutics, 12(2), 663. https://doi.org/10.1021/mp5008426
Tuncel, Sinem, et al. "Correction to "assessing the dual activity of a chalcone-phthalocyanine conjugate: design, synthesis, and antivascular and photodynamic properties"." Molecular pharmaceutics vol. 12,2 (2015): 663. doi: https://doi.org/10.1021/mp5008426
Tuncel S, Trivella A, Atilla D, Bennis K, Savoie H, Albrieux F, Delort L, Billard H, Dubois V, Ahsen V, Caldefie-Chézet F, Richard C, Boyle RW, Ducki S, Dumoulin F. Correction to "assessing the dual activity of a chalcone-phthalocyanine conjugate: design, synthesis, and antivascular and photodynamic properties". Mol Pharm. 2015 Feb 02;12(2):663. doi: 10.1021/mp5008426. Epub 2015 Jan 15. PMID: 25590168.
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New stable reagents for the nucleophilic trifluoromethylation. 1. Trifluoromethylation Of carbonyl compounds with N-formylmorpholine derivatives.

Organic letters

Billard T, Bruns S, Langlois BR.
PMID: 10891240
Org Lett. 2000 Jul 13;2(14):2101-3. doi: 10.1021/ol005987o.

A new stable equivalent of the trifluoromethyl anion has been synthesized from fluoroform. It reacts with nonenolizable carbonyl compounds such as the Ruppert's reagent.

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Billard T, Bruns S, Langlois BR. New stable reagents for the nucleophilic trifluoromethylation. 1. Trifluoromethylation Of carbonyl compounds with N-formylmorpholine derivatives. Org Lett. 2000;2(14):2101-3doi: 10.1021/ol005987o.
Billard, T., Bruns, S., & Langlois, B. R. (2000). New stable reagents for the nucleophilic trifluoromethylation. 1. Trifluoromethylation Of carbonyl compounds with N-formylmorpholine derivatives. Organic letters, 2(14), 2101-3. https://doi.org/10.1021/ol005987o
Billard, et al. "New stable reagents for the nucleophilic trifluoromethylation. 1. Trifluoromethylation Of carbonyl compounds with N-formylmorpholine derivatives." Organic letters vol. 2,14 (2000): 2101-3. doi: https://doi.org/10.1021/ol005987o
Billard T, Bruns S, Langlois BR. New stable reagents for the nucleophilic trifluoromethylation. 1. Trifluoromethylation Of carbonyl compounds with N-formylmorpholine derivatives. Org Lett. 2000 Jul 13;2(14):2101-3. doi: 10.1021/ol005987o. PMID: 10891240.
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A synthetic entry to furo[2,3-b]pyridin-4(1H)-ones and related furoquinolinones via iodocyclization.

Organic letters

Aillaud I, Bossharth E, Conreaux D, Desbordes P, Monteiro N, Balme G.
PMID: 16524281
Org Lett. 2006 Mar 16;8(6):1113-6. doi: 10.1021/ol053048w.

[reaction: see text] N-Methyl-4-alkoxy-3-alkynylpyridin-2(1H)-ones readily undergo iodine-promoted 5-endo-heteroannulation under mild conditions to 3-iodofuropyridinium triiodide salts in moderate to good yields. The latter may be dealkylated in situ upon exposure to an iodide anion to provide the corresponding 3-iodofuro[2,3-b]pyridin-4(1H)-ones. The...

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Aillaud I, Bossharth E, Conreaux D, et al. A synthetic entry to furo[2,3-b]pyridin-4(1H)-ones and related furoquinolinones via iodocyclization. Org Lett. 2006;8(6):1113-6doi: 10.1021/ol053048w.
Aillaud, I., Bossharth, E., Conreaux, D., Desbordes, P., Monteiro, N., & Balme, G. (2006). A synthetic entry to furo[2,3-b]pyridin-4(1H)-ones and related furoquinolinones via iodocyclization. Organic letters, 8(6), 1113-6. https://doi.org/10.1021/ol053048w
Aillaud, Isabelle, et al. "A synthetic entry to furo[2,3-b]pyridin-4(1H)-ones and related furoquinolinones via iodocyclization." Organic letters vol. 8,6 (2006): 1113-6. doi: https://doi.org/10.1021/ol053048w
Aillaud I, Bossharth E, Conreaux D, Desbordes P, Monteiro N, Balme G. A synthetic entry to furo[2,3-b]pyridin-4(1H)-ones and related furoquinolinones via iodocyclization. Org Lett. 2006 Mar 16;8(6):1113-6. doi: 10.1021/ol053048w. PMID: 16524281.
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Influence of structure on the optical limiting properties of nanotubes.

Optics letters

Izard N, Billaud P, Riehl D, Anglaret E.
PMID: 16007790
Opt Lett. 2005 Jun 15;30(12):1509-11. doi: 10.1364/ol.30.001509.

We investigate the role of carbon nanotubes structure on their optical limiting properties. Samples of different and well-characterized structural features are studied by optical limiting and pump-probe experiments. The influence of the diameter's size on the nano-object is demonstrated....

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Izard N, Billaud P, Riehl D, et al. Influence of structure on the optical limiting properties of nanotubes. Opt Lett. 2005;30(12):1509-11doi: 10.1364/ol.30.001509.
Izard, N., Billaud, P., Riehl, D., & Anglaret, E. (2005). Influence of structure on the optical limiting properties of nanotubes. Optics letters, 30(12), 1509-11. https://doi.org/10.1364/ol.30.001509
Izard, N, et al. "Influence of structure on the optical limiting properties of nanotubes." Optics letters vol. 30,12 (2005): 1509-11. doi: https://doi.org/10.1364/ol.30.001509
Izard N, Billaud P, Riehl D, Anglaret E. Influence of structure on the optical limiting properties of nanotubes. Opt Lett. 2005 Jun 15;30(12):1509-11. doi: 10.1364/ol.30.001509. PMID: 16007790.
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Extraction of lanthanides from aqueous solution by using room-temperature ionic liquid and supercritical carbon dioxide in conjunction.

Chemistry (Weinheim an der Bergstrasse, Germany)

Mekki S, Wai CM, Billard I, Moutiers G, Burt J, Yoon B, Wang JS, Gaillard C, Ouadi A, Hesemann P.
PMID: 16311989
Chemistry. 2006 Feb 08;12(6):1760-6. doi: 10.1002/chem.200500559.

For the first time, the study of a three-step extraction system of water/ionic liquid/supercritical CO2 has been performed. Extraction of trivalent lanthanum and europium from an aqueous nitric acid solution to a supercritical CO2 phase via an imidazolium-based ionic...

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Mekki S, Wai CM, Billard I, et al. Extraction of lanthanides from aqueous solution by using room-temperature ionic liquid and supercritical carbon dioxide in conjunction. Chemistry. 2006;12(6):1760-6doi: 10.1002/chem.200500559.
Mekki, S., Wai, C. M., Billard, I., Moutiers, G., Burt, J., Yoon, B., Wang, J. S., Gaillard, C., Ouadi, A., & Hesemann, P. (2006). Extraction of lanthanides from aqueous solution by using room-temperature ionic liquid and supercritical carbon dioxide in conjunction. Chemistry (Weinheim an der Bergstrasse, Germany), 12(6), 1760-6. https://doi.org/10.1002/chem.200500559
Mekki, Soufiane, et al. "Extraction of lanthanides from aqueous solution by using room-temperature ionic liquid and supercritical carbon dioxide in conjunction." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 12,6 (2006): 1760-6. doi: https://doi.org/10.1002/chem.200500559
Mekki S, Wai CM, Billard I, Moutiers G, Burt J, Yoon B, Wang JS, Gaillard C, Ouadi A, Hesemann P. Extraction of lanthanides from aqueous solution by using room-temperature ionic liquid and supercritical carbon dioxide in conjunction. Chemistry. 2006 Feb 08;12(6):1760-6. doi: 10.1002/chem.200500559. PMID: 16311989.
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Showing 1 to 12 of 247 entries