Works matching DE "MICELLAR catalysis"
Results: 140
Biocatalysis in Non‐Conventional Media: Unlocking the Potential for Sustainable Chiral Amine Synthesis.
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- Chemistry - A European Journal, 2024, v. 30, n. 52, p. 1, doi. 10.1002/chem.202304364
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Micelle‐Promoted Reductive Amination of DNA‐Conjugated Amines for DNA‐Encoded Library Synthesis.
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- Chemistry - A European Journal, 2024, v. 30, n. 21, p. 1, doi. 10.1002/chem.202400239
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Sustainable and Bench‐Stable Photoactive Aqueous Nanoaggregates of Cu(II) for ppm Level Cu(I) Catalysis in Water (Adv. Funct. Mater. 36/2022).
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- Advanced Functional Materials, 2022, v. 32, n. 36, p. 1, doi. 10.1002/adfm.202270202
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Synthesis and crystallization-driven solution self-assembly of PE-b-PMMA: controlling Micellar morphology through crystallization temperature and molar mass.
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- Journal of Polymer Research, 2020, v. 27, n. 5, p. 1, doi. 10.1007/s10965-020-02124-2
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MICELLAR EFFECT ON OXIDATION OF SULPHAPYRIDINE IN THE PRESENCE OF PERCHLORIC ACID MEDIUM.
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- Oxidation Communications, 2018, v. 41, n. 1, p. 53
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Cross-Coupling Reaction of Hydrophobic Substrates in Water: Micellar Catalysis with Macromolecular Surfactants.
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- Russian Journal of General Chemistry, 2024, v. 94, p. S148, doi. 10.1134/S1070363224140159
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A New Mn–Salen Micellar Nanoreactor for Enantioselective Epoxidation of Alkenes in Water.
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- Catalysts (2073-4344), 2018, v. 8, n. 4, p. 129, doi. 10.3390/catal8040129
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Optimizing homologous alcohol oxidation: elucidating the impact of surfactant-alcohol hydrophobic interaction and micellar surface charge: Optimizing homologous alcohol oxidation: elucidating the...: M. Layek et al.
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- Research on Chemical Intermediates, 2025, v. 51, n. 1, p. 311, doi. 10.1007/s11164-024-05461-9
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KINETICS OF PENTAAMMINE COBALT(III) COMPLEXES OF α-HYDROXY ACIDS BY ISOQUINOLINIUM FLUOROCHROMATE IN MICELLAR MEDIUM.
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- Rasayan Journal of Chemistry, 2019, v. 12, n. 3, p. 1127, doi. 10.31788/RJC.2019.1235318
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Controllable Fabrication of Various Supramolecular Nanostructures Based on Nonamphiphilic Azobenzene Derivatives and Pillar[6]arene.
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- Chinese Journal of Chemistry, 2015, v. 33, n. 1, p. 107, doi. 10.1002/cjoc.201400508
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Second-order advantage in determining Co (II) in real samples using kinetic-spectrophotometric data matrices and multivariate curve resolution-alternating least square approach.
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- Journal of the Iranian Chemical Society, 2016, v. 13, n. 4, p. 679, doi. 10.1007/s13738-015-0780-z
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Effect of Chaotropes on Lipase Back Extraction Recovery in the Process of Reverse Micellar Extraction.
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- Applied Biochemistry & Biotechnology, 2014, v. 172, n. 6, p. 3287, doi. 10.1007/s12010-014-0738-0
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Multidimensional polyaniline structures from micellar templates.
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- Journal of Materials Science, 2017, v. 52, n. 6, p. 2995, doi. 10.1007/s10853-016-0550-z
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Inhibition of amyloid aggregation of bovine serum albumin by sodium dodecyl sulfate at submicellar concentrations.
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- Biochemistry (00062979), 2018, v. 83, n. 1, p. 60, doi. 10.1134/S000629791801008X
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ACETYLCHOLINESTERASE REACTIVATORS BASED ON OXIME-FUNCTIONALIZED BIODEGRADABLE IONIC LIQUIDS.
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- Military Medical Science Letters / Vojenské zdravotnické Listy, 2018, v. 87, p. 87
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Birefringence study on lyotropic micellar nematic phase in a binary mixture.
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- Phase Transitions, 2015, v. 88, n. 7, p. 653, doi. 10.1080/01411594.2015.1020309
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FORMATION AND CHARACTERISATION OF A STABLE AQUEOUS DISPERSION OF SILVER NANOPARTICLES IN AQUEOUS AND MICELLAR MEDIA. A KINETIC STUDY.
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- Oxidation Communications, 2016, v. 39, n. 1-I, p. 62
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Reactivity of Inorganic α-Nucleophiles in Acyl Transfer in Aqueous and Micellar Media: IV. Peroxyhydrolysis of Acyl Derivatives in Organized Microheterogeneous Systems<sup>1</sup>.
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- Russian Journal of Organic Chemistry, 2024, v. 60, n. 2, p. 252, doi. 10.1134/S1070428024020106
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Chemoselective Synthesis of Alkylphosphinic Acids from Red Phosphorus and Alkyl Bromides in the System KOH/H<sub>2</sub>O/Toluene/Micellar Catalyst.
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- Russian Journal of Organic Chemistry, 2022, v. 58, n. 2, p. 192, doi. 10.1134/S1070428022020063
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Reactivity of Inorganic α-Nucleophiles in Acyl Transfer Processes in Water and Surfactant Micelles: III. Systems Based on Dimeric Cationic Imidazolium Surfactants in Alkaline Hydrolysis of Ethyl 4-Nitrophenyl Ethylphosphonate.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 3, p. 338, doi. 10.1134/S1070428021030039
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Micelle-Catalyzed Synthesis of Arylmethylidene Derivatives of Malononitrile Trimer and Study of Their Optical Properties.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 5, p. 763, doi. 10.1134/S1070428020050061
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Synthesis of 3-Arylcyclopropane-1,1,2,2-tetracarbonitriles under Micellar Catalysis.
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- Russian Journal of Organic Chemistry, 2018, v. 54, n. 12, p. 1839, doi. 10.1134/S1070428018120187
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The Catalytic Influence of Polymers and Surfactants on the Rate Constants of Reaction of Maltose with Cerium (IV) in Acidic Aqueous Medium.
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- Journal of Chemistry, 2022, p. 1, doi. 10.1155/2022/2609478
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MICELLIZATION BEHAVIOUR OF CONVENTIONAL (SDS AND DTAB) AND SYNTHESIZED GEMINI SURFACTANT (12-2-12) IN AQUEOUS SOLUTIONS OF METFORMIN HYDROCHLORIDE AT VARYING TEMPERATURES: A COMPARATIVE STUDY.
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- Journal of Advanced Scientific Research, 2022, v. 13, n. 1, p. 125, doi. 10.55218/JASR.202213113
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An Environmentally Friendly Method for the Determination of Pentachlorophenol in Paper Packaging Materials Using Ultrasonic-Assisted Micellar Extraction.
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- Journal of Chromatographic Science, 2015, v. 53, n. 10, p. 1808, doi. 10.1093/chromsci/bmv076
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Verteilungsgleichgewichte von Liganden in mizellaren Lösungsmittelsystemen Equilibrium Distribution of Ligands in Micellar Solutions.
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- Chemie Ingenieur Technik (CIT), 2016, v. 88, n. 1/2, p. 119, doi. 10.1002/cite.201500125
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Effect of cyclodextrins' cavity on the kinetics of alkaline hydrolysis of tris(1,10-Phenanthroline)Fe(II) in presence of surfactant.
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- Journal of Dispersion Science & Technology, 2023, v. 44, n. 6, p. 1054, doi. 10.1080/01932691.2021.1993891
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Influence of dimeric gemini surfactant micelles on the study of nickel-glycylleucine dipeptide and ninhydrin.
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- Journal of Dispersion Science & Technology, 2020, v. 41, n. 10, p. 1559, doi. 10.1080/01932691.2019.1627886
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Removal of tetramethyl ammonium hydroxide from synthetic liquid wastes of electronic industry through micellar enhanced ultrafiltration.
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- Journal of Dispersion Science & Technology, 2018, v. 39, n. 2, p. 207, doi. 10.1080/01932691.2017.1307760
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Physicochemical Investigation of the Micellar Behavior of a Diblock (PEO) 62 -b-(PBO) 33 Copolymer in Water and its Interaction with Ionic Surfactants.
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- Journal of Dispersion Science & Technology, 2016, v. 37, n. 4, p. 519, doi. 10.1080/01932691.2015.1048460
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Application of differential spectra from two different environments in simultaneous quantification of new fuchsine, crystal violet and malachite green in the presence of unmodeled interferents using first order multivariate calibration method.
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- Journal of Analytical Chemistry, 2015, v. 70, n. 1, p. 44, doi. 10.1134/S1061934815010190
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From Electronic Waste to Suzuki−Miyaura Cross‐Coupling Reaction in Water: Direct Valuation of Recycled Palladium in Catalysis.
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- ChemSusChem, 2020, v. 13, n. 19, p. 5133, doi. 10.1002/cssc.202002039
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Synthesis and micellar characterization of luteinizing hormone-releasing hormone poly(ethylene glycol)- block-poly( l-histidine) copolymers.
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- Polymer Engineering & Science, 2015, v. 55, n. 2, p. 277, doi. 10.1002/pen.23892
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Polyoxometalate-Based Metal-Organic Frameworks as Catalysts for the Selective Oxidation of Alcohols in Micellar Systems.
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- ChemPlusChem, 2014, v. 79, n. 6, p. 872, doi. 10.1002/cplu.201400009
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Lösungsmittel: Weder Dystopie noch Nirwana.
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- Nachrichten aus der Chemie, 2022, v. 70, n. 3, p. 28, doi. 10.1002/nadc.20224122452
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- Article
Micellar effect on pentavalent vanadium oxidation of formaldehyde to formic acid in aqueous acid media at room temperature.
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- Research on Chemical Intermediates, 2015, v. 41, n. 8, p. 5331, doi. 10.1007/s11164-014-1635-4
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Micellar catalysis of quinquivalent vanadium oxidation of methanol to formaldehyde in aqueous medium.
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- Research on Chemical Intermediates, 2015, v. 41, n. 8, p. 5565, doi. 10.1007/s11164-014-1682-x
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Choice of suitable micellar catalyst for 2,2′-bipyridine-promoted chromic acid oxidation of glycerol to glyceraldehyde in aqueous media at room temperature.
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- Research on Chemical Intermediates, 2015, v. 41, n. 5, p. 3057, doi. 10.1007/s11164-013-1415-6
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Micellar Catalysis Strategy of Cross-Condensation Reaction: The Effect of Polar Heads on the Catalytic Properties of Aminoalcohol-Based Surfactants.
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- Catalysis Letters, 2020, v. 150, n. 5, p. 1309, doi. 10.1007/s10562-019-03045-6
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Kinetic Investigation of Micellar Promoted Pyridine based Oximate and Hydroxamate Catalysis on Phosphotriester Pesticides.
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- Catalysis Letters, 2017, v. 147, n. 2, p. 602, doi. 10.1007/s10562-016-1912-5
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Highly Selective Hydrogenation of α-Pinene Catalyzed by Ru Nanoparticles in Aqueous Micellar Microreactors.
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- Catalysis Letters, 2016, v. 146, n. 3, p. 580, doi. 10.1007/s10562-015-1685-2
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Micellar Catalysis and Reactivity in Nanostructured Ionic Liquids: Two Sides of the Same Coin?
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- Australian Journal of Chemistry, 2022, v. 75, n. 2, p. 9, doi. 10.1071/CH21109
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Folate-conjugated pH-controllable fluorescent nanomicelles acting as tumor targetable drug carriers.
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- Microchimica Acta, 2017, v. 184, n. 8, p. 2881, doi. 10.1007/s00604-017-2255-7
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Vesicular and micellar self‐assembly of stimuli‐responsive poly(<italic>N</italic>‐isopropyl acrylamide‐<italic>b</italic>‐9‐anthracene methyl methacrylate) amphiphilic diblock copolymers.
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- Journal of Applied Polymer Science, 2018, v. 135, n. 28, p. 1, doi. 10.1002/app.46474
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Understanding the Metal Distribution in Core-Shell Nanoparticles Prepared in Micellar Media.
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- Nanoscale Research Letters, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s11671-015-1048-3
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Numerical Simulation of Surfactant Adsorption in Micellar Polymer Flooding.
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- Energy Sources Part A: Recovery, Utilization & Environmental Effects, 2014, v. 36, n. 16, p. 1774, doi. 10.1080/15567036.2011.559526
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A Supramolecular Approach to the Preparation of Nanographene Adlayers Using Water‐Soluble Molecular Capsules.
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- Angewandte Chemie, 2018, v. 130, n. 47, p. 15707, doi. 10.1002/ange.201809258
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Generating Hydrated Electrons for Chemical Syntheses by Using a Green Light‐Emitting Diode (LED).
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- Angewandte Chemie, 2018, v. 130, n. 4, p. 1090, doi. 10.1002/ange.201711692
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- Article
Block Copolymer Micellization as a Protection Strategy for DNA Origami.
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- Angewandte Chemie, 2017, v. 129, n. 20, p. 5552, doi. 10.1002/ange.201608873
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- Article
An Improved System for the Aqueous Lipshutz-Negishi Cross-Coupling of Alkyl Halides with Aryl Electrophiles.
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- Angewandte Chemie, 2016, v. 128, n. 5, p. 1881, doi. 10.1002/ange.201509341
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