Search Results - "Pascual, Alfons"

Low-Pressure H2, NH3 Microwave Plasma Treatment of Polytetrafluoroethylene (PTFE) Powders: Chemical, Thermal and Wettability Analysis by Hunke, Harald, Soin, Navneet, Shah, Tahir, Kramer, Erich, Pascual, Alfons, Karuna, Mallampalli, Siores, Elias

“…Functionalization of Polytetrafluoroethylene (PTFE) powders of ~6 μm particle size is carried out using low-pressure 2.45 GHz H2, NH3 microwave plasmas for…”
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On the stability of PEEK for short processing cycles at high temperatures and oxygen-containing atmosphere by Pascual, Alfons, Toma, Michael, Tsotra, Panayota, Grob, Markus C.

“…The motivation of this study was to investigate the stability of poly(ether ether ketone) (PEEK) at conditions close to real processing: fast cycles (below…”
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Short synthesis of 4-chloro-4′-(chlorodifluoromethoxy)benzophenone by Karrer, Friedrich, Meier, Hans, Pascual, Alfons

“…A one-pot, highly selective synthesis of 4-chloro-4′-(chlorodifluoromethoxy)benzophenone suitable for an industrial scale-up was developed. Fluorination of…”
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Ultraviolet-ozone surface cleaning of injection-molded, thermoplastic microcantilevers by Urwyler, Prabitha, Pascual, Alfons, Müller, Bert, Schift, Helmut

“…ABSTRACT Ultraviolet–ozone (UVO) is used for the cleaning of labware from organic contamination and includes sterilization, surface roughening, and activation…”
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Mechanical and chemical stability of injection-molded microcantilevers used for sensing by Urwyler, Prabitha, Pascual, Alfons, Kristiansen, Per Magnus, Gobrecht, Jens, Müller, Bert, Schift, Helmut

“…Ultraviolet‐ozone treatment is used as a standard surface cleaning procedure for removal of molecular organic contamination from analytical and sensing…”
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Substituted α-(phenylhydrazono)phenylacetonitrile derivatives. Part 1: A new class of uncoupler of oxidative phosphorylation by Danko, Peter, Flury, Thomas, Hall, Roger G, Karrer, Friedrich, Kienast, Heinz, Kriz, Miroslav, Leuenberger, Katrin, Pascual, Alfons, Steiger, Arthur, Trah, Stephan

“…Substituted α‐(phenylhydrazono)phenylacetonitrile derivatives have been discovered which constitute a series of potent uncouplers of oxidative phosphorylation…”
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Substituted α-(phenylhydrazono)phenylacetonitrile derivatives. Part 2: synthesis and biological activity of pro-pesticides by Flury, Thomas, Hall, Roger G, Karrer, Friedrich, Kienast, Heinz, Leuenberger, Katrin, Pascual, Alfons, Rindlisbacher, Alfred, Trah, Stephan, Widmer, Hans-Joerg

“…Pro‐pesticides of α‐(2,6‐dichloro‐4‐trifluoromethylphenylhydrazono)‐4‐nitrophenylacetonitrile have been prepared and tested against mite and insect pests…”
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Substituted α- (phenylhydrazono)phenyl-acetonitrile derivatives. Part 1: A new class of uncoupler of oxidative phosphorylation by DANKO, Peter, FLURY, Thomas, HALL, Roger G, KARRER, Friedrich, KIENAST, Heinz, KRIZ, Miroslav, LEUENBERGER, Katrin, PASCUAL, Alfons, STEIGER, Arthur, TRAH, Stephan

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Substituted α- (phenylhydrazono)phenylaceto- nitrile derivatives. Part 2: Synthesis and biological activity of pro-pesticides by FLURY, Thomas, HALL, Roger G, KARRER, Friedrich, KIENAST, Heinz, LEUENBERGER, Katrin, PASCUAL, Alfons, RINDLISBACHER, Alfred, TRAH, Stephan, WIDMER, Hans-Joerg

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Synthesis of 8-substituted 5H,9H-6-oxa-7-aza-benzocyclononene-10,11-dione-11-O-methyloximes, a new [1,2]-oxazonine ring system by Pascual, Alfons, Ziegler, Hugo, Trah, Stephan, Ertl, Peter, Winkler, Tammo

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Synthesis of 8-substituted 5 H,9 H-6-oxa-7-aza-benzocyclononene-10,11-dione-11- O-methyloximes, a new [1,2]-oxazonine ring system by Pascual, Alfons, Ziegler, Hugo, Trah, Stephan, Ertl, Peter, Winkler, Tammo

“…Reaction of (2-bromomethyl-phenyl)-methoxyimino-acetic acid methyl ester 4 with oximes 1 in the presence of NaH/DMF yields 8-substituted 5 H,9…”
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Synthesis and structure-activity relationships of benzophenone hydrazone derivatives with insecticidal activity by Böger, Manfred, Dürr, Dieter, Gsell, Laurenz, Hall, Roger G, Karrer, Friedrich, Kristiansen, Odd, Maienfisch, Peter, Pascual, Alfons, Rindlisbacher, Alfred

“…A broad range of benzophenone hydrazone derivatives was prepared and tested against selected chewing insect pests, allowing the analysis of structure‐activity…”
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Synthese des 5‐[(Acetylhydrazono)‐(4‐chlorphenyl)‐methyl]thiophen‐2‐yl‐esters der Trifluormethansulfonsäure by Pascual, Alfons

“…The synthesis of 5‐[(acetylhydrazono)‐(4‐chlorophenyl)‐methyl]thiophen‐2‐yl ester of the trifluoromethanesulfonic acid (2a) and its N‐methyl derivative 2b was…”
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Synthesis and insecticidal activity of 4-perhaloalkoxy (or thioalkyl) benzophenonehydrazone derivatives by Dürr, Dieter, Gsell, Laurenz, Hall, Roger G, Karrer, Friedrich, Pascual, Alfons, Rindlisbacher, Alfred

“…Benzophenonehydrazone derivatives containing a mesylate or triflate substituent are known to exhibit insecticidal activity. In the present study, such…”
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Synthese des 5-[(Acetylhydrazono)-(4-chlorphenyl)-methyl]thiophen-2-yl-esters der Trifluormethansulfonsäure by Pascual, Alfons

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