화학공학소재연구정보센터
검색결과 : 21건
No. Article
1 Recognizing alchemy
Lattes A
Chemical & Engineering News, 94(23), 4, 2016
2 Gelled oil particles: A new approach to encapsulate a hydrophobic metallophthalocyanine
Siqueira-Moura MP, Franceschi-Messant S, Blanzat M, Re MI, Perez E, Rico-Lattes I, Lattes A, Tedesco AC
Journal of Colloid and Interface Science, 401, 155, 2013
3 Functionalized Vesicles Based on Amphiphilic Boronic Acids: A System for Recognizing Biologically Important Polyols
Savsunenko O, Matondo H, Franceschi-Messant S, Perez E, Popov AF, Rico-Lattes I, Lattes A, Karpichev Y
Langmuir, 29(10), 3207, 2013
4 Assessment of biogas potential hazards
Naja GM, Alary R, Bajeat P, Bellenfant G, Godon JJ, Jaeg JP, Keck G, Lattes A, Leroux C, Modelon H, Moletta-Denat M, Ramalho O, Rousselle C, Wenisch S, Zdanevitch I
Renewable Energy, 36(12), 3445, 2011
5 Study of hydrogen bonding in liquid crystalline solvent by Fourier transform infrared spectroscopy
Palaprat G, Marty JD, Routaboul C, Lattes A, Mingotaud AF, Mauzac M
Journal of Physical Chemistry A, 110(47), 12887, 2006
6 Complexes between beta-cyclodextrin and aliphatic guests as new noncovalent amphiphiles: Formation and physicochemical studies
Bojinova T, Coppel Y, Lauth-de Viguerie N, Milius A, Rico-Lattes I, Lattes A
Langmuir, 19(13), 5233, 2003
7 Aggregation behavior in aqueous solutions of a new class of asymmetric bipolar amphiphiles investigated by surface tension measurements
Gouzy MF, Guidetti B, Andre-Barres C, Rico-Lattes I, Lattes A, Vidal C
Journal of Colloid and Interface Science, 239(2), 517, 2001
8 Reactivity at the interface of chiral amphiphilic dendrimers. High asymmetric reduction by NaBH4 of various prochiral ketones
Schmitzer AR, Franceschi S, Perez E, Rico-Lattes I, Lattes A, Thion L, Erard M, Vidal C
Journal of the American Chemical Society, 123(25), 5956, 2001
9 Aggregation behavior of urocanic acid bolaamphiphiles
Sirieix J, Lauth-de Viguerie N, Riviere M, Lattes A
Langmuir, 16(24), 9221, 2000
10 New catanionic glycolipids. 1. Synthesis, characterization, and biological activity of double-chain and gemini catanionic analogues of galactosylceramide (gal beta(1)cer)
Blanzat M, Perez E, Rico-Lattes I, Prome D, Prome JC, Lattes A
Langmuir, 15(19), 6163, 1999