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See detailSynthesis of glucose-responsive hollow capsules
Alaimo, David ULg; Detrembleur, Christophe ULg; Auzély-Velty, Rachel et al

Poster (2009, December 07)

Detailed reference viewed: 12 (1 ULg)
See detailSynthesis of growth hormone by bacteria
Seeburg, P. H.; Shine, J.; Martial, Joseph ULg et al

in Nature (1978), 276(5690), 795-8

A hybrid gene was constructed between the beta-lactamase gene of plasmid pBR322 and the cloned coding sequence for rat growth hormone. This gene is expressed in bacteria and growth hormone sequences are ... [more ▼]

A hybrid gene was constructed between the beta-lactamase gene of plasmid pBR322 and the cloned coding sequence for rat growth hormone. This gene is expressed in bacteria and growth hormone sequences are detectable by immunological methods. [less ▲]

Detailed reference viewed: 32 (1 ULg)
See detailSynthesis of high specificity tritium labelled chloroethylcyclohexylnitrosourea and its application to the study of DNA modification
Siew, E.; Habraken, Yvette ULg; Ludlum, D.

in Journal of the radiolabelled compounds and radiopharmaceuticals (1991), XXIX

Detailed reference viewed: 4 (0 ULg)
See detailSynthesis of high-relaxivity contrast agents for magnetic resonance imaging by "click" chemistry
Vanasschen, Christian; Thonon, David ULg; Lecomte, Philippe ULg et al

Poster (2007, August 31)

Detailed reference viewed: 48 (7 ULg)
See detailSynthesis of highly dispersed Pd/SiO2 cogelled xerogel catalysts from various silylated ligands
Lambert, Stéphanie ULg; Tran, Kim Yên; Arrachart, Guilhem et al

Poster (2007)

Detailed reference viewed: 12 (3 ULg)
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See detailSynthesis of highly functionalized poly(alkyl cyanoacrylate) nanoparticles by means of click chemistry
Nicolas, Julien; Bensaid, Fehti; Desmaële, Didier et al

in Macromolecules (2008), 41(22), 8418-8428

A general methodology was proposed to prepare highly functionalized poly(alkyl cyanoacrylate) nanoparticles by means of Huisgen 1,3-dipolar cyclo-addition, the so-called click chemistry. To achieve this ... [more ▼]

A general methodology was proposed to prepare highly functionalized poly(alkyl cyanoacrylate) nanoparticles by means of Huisgen 1,3-dipolar cyclo-addition, the so-called click chemistry. To achieve this goal, different protocols were investigated to obtain azidopoly(ethylene glycol) cyanoacetate of variable molar mass, followed by a Knoevenagel condensation−Michael addition reaction with hexadecyl cyanoacetate to produce a poly[(hexadecyl cyanoacrylate)-co-azidopoly(ethylene glycol) cyanoacrylate] (P(HDCA-co-N3PEGCA)) copolymer, displaying azide functionalities at the extremity of the PEG chains. As a proof of concept, model alkynes were quantitatively coupled either to the P(HDCA-co-N3PEGCA) copolymers in homogeneous medium followed by self-assembly in aqueous solution or directly at the surface of the preformed P(HDCA-co-N3PEGCA) nanoparticles in aqueous dispersed medium, both yielding highly functionalized nanoparticles. This versatile approach, using alkyl cyanoacrylate derivatives, opened the door to ligand-functionalized and biodegradable nanoparticles with “stealth” properties for biomedical applications. [less ▲]

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See detailSynthesis of highly ordered mesoporous compounds with control of morphology using a non-ionic surfactant as template
Léonard, Alexandre ULg; Blin, J. L.; Su, B.-L.

in Studies in Surface Science and Catalysis (2002), 141

Highly ordered hexagonal mesostructures (CMI-1 compounds) can be obtained under mild acidic conditions by working at low concentrations of non-ionic decaoxyethylene cetyl ether [C16(EO)10]. The present ... [more ▼]

Highly ordered hexagonal mesostructures (CMI-1 compounds) can be obtained under mild acidic conditions by working at low concentrations of non-ionic decaoxyethylene cetyl ether [C16(EO)10]. The present work shows that it is possible to gain control at the nanometer scale over the packing symmetry of the channels, as well as at the micrometer level over the morphology of the particles by varying the surfactant / silica molar ratio and the hydrothermal treatment conditions. Very high loadings of silica precursors typically afford highly ordered hexagonal CMI-1 compounds whereas an increase of the surfactant / silica molar ratio results in materials with a more disordered channel array. In a parallel way, very low molar ratios of surfactant / silica lead to ropes, gyroids and toroids whereas spheres are the most stable shape with the lower quantities of silica. From this point, it appears thus that not only the structure but also the morphologies encountered for MCM-41 type mesoporous silica can be reproduced with a non-ionic templating agent. [less ▲]

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See detailSynthesis of La0.9Sr0.1Ga0.8Mg0.2O2.85 by successive freeze-drying and self-ignition of a hydroxypropylmethyl cellulose solution
Traina, Karl ULg; Steil, M. C.; Pirard, Jean-Paul ULg et al

in Journal of the European Ceramic Society (2007), 27(12), 3469-3474

The present paper reports the synthesis of La0.9Sr0.1Ga0.8Mg0.2O2.85 perovskite powders by a method combining freeze-drying and self-ignition of an aqueous solution of metallic nitrates containing ... [more ▼]

The present paper reports the synthesis of La0.9Sr0.1Ga0.8Mg0.2O2.85 perovskite powders by a method combining freeze-drying and self-ignition of an aqueous solution of metallic nitrates containing hydroxypropylmethyl cellulose. The precursor powder obtained after self-ignition was submitted to various thermal treatments and the resulting powders were characterized by X-ray diffraction, electron microscopy, nitrogen adsorption-desorption isotherm analysis, mercury porosimetry and laser granulometry. It turns out that this synthesis method yields single-phase powders with good homogeneity and sinterability properties. The precursor powder treated at 1200 degrees C presents a coral-like structure which collapses under application of low uniaxial pressure, resulting in a narrow grain size distribution suitable for sintering (98.8% relative density for a pellet sintered at 1400 degrees C during 1 h). The fact that no milling step is necessary is an additional advantage of this method, which shows promising prospects for the synthesis of other multicationic oxides. (c) 2007 Elsevier Ltd. All rights reserved. [less ▲]

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See detailSynthesis of large pore disordered MSU-type mesoporous silicas through the assembly of C16(EO)10 surfactant and TMOS silica source: Effect of the hydrothermal treatment and thermal stability of materials
Blin, J. L.; Léonard, Alexandre ULg; Su, B. L.

in Journal of Physical Chemistry B (2001), 105(26), 6070-6079

Decaoxyethylene cetyl ether [C 16(EO) 10] has been employed as templating agent for large pore disordered MSU-type mesoporous silicas synthesis. The effect of the hydrothermal treatment (heating time and ... [more ▼]

Decaoxyethylene cetyl ether [C 16(EO) 10] has been employed as templating agent for large pore disordered MSU-type mesoporous silicas synthesis. The effect of the hydrothermal treatment (heating time and temperature) on the textural properties, in particular, pore diameter of materials has been investigated. The obtained materials have been characterized by different techniques such as X-ray diffraction, scanning and transmission electron microscopy and nitrogen adsorption-desorption analysis. The thermal stability of the compounds is also evaluated. Our results show that the pore diameter depends strongly on the heating time and temperature. This is the result of a competition between the stretching of the surfactant chains, which can lead to the breakdown of the walls separating adjacent pores, and the reorganization of micelles with heating time and temperature. At higher temperature or for longer durations, a more extended surfactant molecular conformation can be obtained, which leads to materials with larger pore sizes. A reorganization of the micellar solution during the hydrothermal treatment in autoclave can also simultaneously occur to give materials with smaller pore diameter. It is found that compounds prepared with the nonionic surfactant exhibit an enhanced thermal stability compared to those synthesized with cetyltrimethylammonium bromide (CTMABr) as templating agent. This higher stability is related to the synthesis pathway and the structure of materials. [less ▲]

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See detailSynthesis of macrocyclic poly(epsilon-caprolactone) by intramolecular cross-linking of unsaturated end groups of chains precyclic by the initiation
Li, Haiying; Debuigne, Antoine ULg; Jérôme, Robert ULg et al

in Angewandte Chemie (International ed. in English) (2006), 45(14), 2264-2267

Detailed reference viewed: 34 (16 ULg)
See detailSynthesis of macrocyclic polyesters
Lecomte, Philippe ULg; Jérôme, Robert ULg

Poster (2003, May 16)

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See detailSynthesis of microsphere-loaded porous polymers by combining emulsion and dispersion polymerisations in supercritical carbon dioxide
Boyère, Cédric ULg; Léonard, Alexandre ULg; Grignard, Bruno ULg et al

in Chemical Communications (2012), 48(67), 8356-8358

Highly porous materials were produced by acrylamide polymerisation templated by supercritical CO2-in-water emulsions using new fluorinated glycosurfactants. Properties of the resulting polymer scaffolds ... [more ▼]

Highly porous materials were produced by acrylamide polymerisation templated by supercritical CO2-in-water emulsions using new fluorinated glycosurfactants. Properties of the resulting polymer scaffolds were tuned by performing dispersion polymerisations within their cavities filled with supercritical CO2. [less ▲]

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See detailSynthesis of Modified Peptidoglycan Precursor Analogues for the Inhibition of Glycosyltransferase.
Dumbre, S; Derouaux, Adeline ULg; Lescrinier, E et al

in Journal of the American Chemical Society (2012)

The peptidoglycan glycosyltransferases (GTs) are essential enzymes that catalyze the polymerization of glycan chains of the bacterial cell wall from lipid II and thus constitute a validated antibacterial ... [more ▼]

The peptidoglycan glycosyltransferases (GTs) are essential enzymes that catalyze the polymerization of glycan chains of the bacterial cell wall from lipid II and thus constitute a validated antibacterial target. Their enzymatic cavity is composed of a donor site for the growing glycan chain (where the inhibitor moenomycin binds) and an acceptor site for lipid II substrate. In order to find lead inhibitors able to fill this large active site, we have synthesized a series of substrate analogues of lipid I and lipid II with variations in the lipid, the pyrophosphate, and the peptide moieties and evaluated their biological effect on the GT activity of E. coli PBP1b and their antibacterial potential. We found several compounds able to inhibit the GT activity in vitro and cause growth defect in Bacillus subtilis . The more active was C16-phosphoglycerate-MurNAc-(l-Ala-d-Glu)-GlcNAc, which also showed antibacterial activity. These molecules are promising leads for the design of new antibacterial GT inhibitors. [less ▲]

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See detailThe Synthesis of N-Benzyl-2-azanorbornene via Aqueous Hetero Diels-Alder Reaction
Sauvage, Xavier ULg; Delaude, Lionel ULg

in Journal of Chemical Education (2008), 85(11), 1538-1540

The synthesis of N-benzyl-2-azanorbornene via aqueous hetero Diels-Alder reaction of cyclopentadiene and benzyliminium chloride formed in situ from benzylamine hydrochloride and formaldehyde is described ... [more ▼]

The synthesis of N-benzyl-2-azanorbornene via aqueous hetero Diels-Alder reaction of cyclopentadiene and benzyliminium chloride formed in situ from benzylamine hydrochloride and formaldehyde is described. Characterization of the product was achieved by IR and NMR spectroscopies. The spectral data acquired are thoroughly discussed. Numerous coupling constants were extracted from the 1H NMR spectrum. They provide a valuable material to familiarize students with the different types of proton-proton coupling patterns and their typical ranges. Karplus type correlations served to calculate 3J vicinal coupling constants as a function of dihedral angles. These computational studies involved molecular modeling. Because the synthetic part is rather straightforward and easy to carry out, this experiment is suitable for an introductory laboratory course where it can serve to illustrate the concepts of green chemistry and atom efficiency. Emphasis can also be placed on structural analysis for use within a spectroscopy course even if there is no activity component associated with it. Last but not least, the whole project provides ample materials for an advanced undergraduate laboratory in green chemistry that combines organic synthesis, structural analysis, and theoretical calculations. [less ▲]

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See detailSynthesis of N-heterocyclic carbene precursors bearing biphenyl units and their use in ruthenium-catalyzed ring-opening metathesis polymerization
Maj, Anna M.; Delaude, Lionel ULg; Demonceau, Albert ULg et al

in Journal of Organometallic Chemistry (2007), 692(14), 3048-3056

A range of new imidazolium and imidazolinium chlorides bearing biphenyl units on their nitrogen atoms was synthesized. They differed by the electron-withdrawing or -donating nature and the steric bulk of ... [more ▼]

A range of new imidazolium and imidazolinium chlorides bearing biphenyl units on their nitrogen atoms was synthesized. They differed by the electron-withdrawing or -donating nature and the steric bulk of the substituents on their aromatic rings. These various N-heterocyclic carbene (NHC) precursors were combined with the [RuCl2(p-cymene)](2) dimer and potassium tert-butoxide to generate the corresponding ruthenium-arene complexes [RuCl2(p-cymene)(NHC)] in situ. The catalytic activity of these species was investigated in the photoinduced ring-opening metathesis polymerization (ROMP) of cyclooctene. The results obtained confirmed the necessity of blocking the ortho-positions of the phenyl rings in the vicinity of the metal center in order to attain high catalytic efficiencies. They also showed that changing the steric and electronic properties of the substituents on the remote phenyl rings of the biphenyl units had no significant influence on the outcome of the polymerization. (C) 2007 Elsevier B.V. All rights reserved. [less ▲]

Detailed reference viewed: 27 (3 ULg)