Works matching DE "DIPHENYLACETYLENE"
Results: 63
Acyclic Boryl Complexes of Copper(I).
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- Chemistry - A European Journal, 2024, v. 30, n. 1, p. 1, doi. 10.1002/chem.202302704
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A Versatile Palladium Synthon: [Pd(NHC)(PhC≡CPh)]**.
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- Chemistry - A European Journal, 2022, v. 28, n. 67, p. 1, doi. 10.1002/chem.202201917
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Dual Photo‐Responsive Diphenylacetylene Enables PET In‐Situ Upcycling with Reverse Enhanced UV‐Resistance and Strength.
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- Angewandte Chemie, 2023, v. 135, n. 52, p. 1, doi. 10.1002/ange.202314448
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Frontispiz: Facile Synthesis of Linear and Cyclic Poly(diphenylacetylene)s by Molybdenum and Tungsten Catalysis.
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- Angewandte Chemie, 2023, v. 135, n. 37, p. 1, doi. 10.1002/ange.202383761
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Titelbild: Tetrazole Diversification of Amino Acids and Peptides via Silver‐Catalyzed Intermolecular Cycloaddition with Aryldiazonium Salts (Angew. Chem. 37/2023).
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- Angewandte Chemie, 2023, v. 135, n. 37, p. 1, doi. 10.1002/ange.202309192
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Facile Synthesis of Linear and Cyclic Poly(diphenylacetylene)s by Molybdenum and Tungsten Catalysis.
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- Angewandte Chemie, 2023, v. 135, n. 37, p. 1, doi. 10.1002/ange.202302332
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Conformational Kinetics in Chiral Poly(diphenylacetylene)s: A Dynamic P/M Memory Effect.
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- Angewandte Chemie, 2023, v. 135, n. 32, p. 1, doi. 10.1002/ange.202307059
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Well‐Controlled Living Polymerization of Phenylacetylenes in Water: Synthesis of Water‐Soluble Stereoregular Telechelic Poly(phenylacetylene)s.
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- Angewandte Chemie, 2022, v. 134, n. 26, p. 1, doi. 10.1002/ange.202202676
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Titelbild: Dissymmetric Chiral Poly(diphenylacetylene)s: Secondary Structure Elucidation and Dynamic Luminescence (Angew. Chem. 9/2022).
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- Angewandte Chemie, 2022, v. 134, n. 9, p. 1, doi. 10.1002/ange.202201134
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Dissymmetric Chiral Poly(diphenylacetylene)s: Secondary Structure Elucidation and Dynamic Luminescence.
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- Angewandte Chemie, 2022, v. 134, n. 9, p. 1, doi. 10.1002/ange.202115070
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Facile and Versatile Synthesis of End‐Functionalized Poly(phenylacetylene)s: A Multicomponent Catalytic System for Well‐Controlled Living Polymerization of Phenylacetylenes.
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- Angewandte Chemie, 2020, v. 132, n. 22, p. 8748, doi. 10.1002/ange.202000361
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Room Temperature Fluorescent Conjugated Polymer Gums.
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- Advanced Functional Materials, 2014, v. 24, n. 13, p. 1928, doi. 10.1002/adfm.201302829
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Selective hydrogenation of diphenylacetylene using NiCo nanoparticles supported on mesoporous carbon as catalyst.
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- Turkish Journal of Chemistry, 2022, v. 46, n. 3, p. 677, doi. 10.55730/1300-0527.3359
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Voltammetric Determination of Metol on a Gold Nanoparticle Modified Carbon Molecular Wire Electrode.
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- Analytical Letters, 2017, v. 50, n. 2, p. 325, doi. 10.1080/00032719.2016.1177536
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Estimation of the Fraction of Spin-Correlated Radical Ion Pairs in Irradiated Alkanes using Magnetosensitive Recombination Luminescence from Exciplexes Generated upon Recombination of a Probe Pair.
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- Zeitschrift für Physikalische Chemie, 2017, v. 231, n. 2, p. 239, doi. 10.1515/zpch-2016-0819
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Palladium-immobilized triazine dendrimer on magnetic nanoparticles: as reusable microreactor for solvent-dependent synthesis strategy of 2,3-diphenylindoles and pentaphenylpyrrole derivatives.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-72224-2
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Solvent‐dependent helix inversion in optically active poly(diphenylacetylene)s and their chiral recognition abilities as chiral stationary phases for high‐performance liquid chromatography.
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- Chirality, 2022, v. 34, n. 4, p. 597, doi. 10.1002/chir.23416
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Single-Atom Alloy Pd 1 Ag 10 /CeO 2 –ZrO 2 as a Promising Catalyst for Selective Alkyne Hydrogenation.
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- Inorganics, 2023, v. 11, n. 4, p. 150, doi. 10.3390/inorganics11040150
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Synthesis of Polycyclic Amides via Tandem Rh<sup>III</sup>-Catalyzed C−H Activation and Annulation from Dioxazolones and Alkynes.
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- Asian Journal of Organic Chemistry, 2017, v. 6, n. 7, p. 812, doi. 10.1002/ajoc.201700140
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Effect of Iodide on the pH-Controlled Hydrogenations of Diphenylacetylene and Cinnamaldehyde Catalyzed by Ru(II)-Sulfonated Triphenylphosphine Complexes in Aqueous–Organic Biphasic Systems.
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- Catalysts (2073-4344), 2022, v. 12, n. 5, p. 518, doi. 10.3390/catal12050518
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Reaction of a Dialumene-Benzene Adduct with Diphenylacetylene: Formation of 3,4-Dialuminacyclobutene and 5,6-Dialuminabicyclo[2.1.1]hex-2-ene Derivatives.
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- Chemistry - An Asian Journal, 2014, v. 9, n. 11, p. 3099, doi. 10.1002/asia.201402798
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Effect of the Substitution Pattern on the.
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- Chemistry - An Asian Journal, 2013, v. 8, n. 12, p. 3164, doi. 10.1002/asia.201300872
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Stereoselective Synthesis of Enamides through Palladium‐Catalyzed Oxidative Amidation of Conjugated Olefins with 2‐Pyridones.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 2, p. 1, doi. 10.1002/ejoc.202201239
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Study of Cyclization of Diphenylacetals Derived from L-rhamnose and L-fucose: A Theoretical Approach.
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- South African Journal of Chemistry, 2012, v. 65, p. 84
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Highly Emissive, Water-Repellent, Soft Materials: Hydrophobic Wrapping and Fluorescent Plasticizing of Conjugated Polyelectrolyte via Electrostatic Self-Assembly.
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- Advanced Functional Materials, 2016, v. 26, n. 25, p. 4501, doi. 10.1002/adfm.201600889
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Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: ( E)-3-benzylidenepyrrolidine-2,5-dione, ( E)-3-benzylidene-1-methylpyrrolidine-2,5-dione and ( E)-3-benzylidene-1- tert-butylpyrrolidine-2,5-dione.
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- Acta Crystallographica Section C: Structural Chemistry, 2016, v. 72, n. 6, p. 504, doi. 10.1107/S2053229616008159
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Bimetallic Nickel-Iridium and Nickel-Osmium Alloy Nanoparticles and Their Catalytic Performance in Hydrogenation Reactions.
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- ChemCatChem, 2017, v. 9, n. 18, p. 3534, doi. 10.1002/cctc.201700168
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SBA-15-Supported Metal Silicides Prepared by Chemical Vapor Deposition as Efficient Catalysts Towards the Semihydrogenation of Phenylacetylene.
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- ChemCatChem, 2017, v. 9, n. 7, p. 1337, doi. 10.1002/cctc.201601653
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Ultrasound- and Microwave-Assisted Preparation of Lead-Free Palladium Catalysts: Effects on the Kinetics of Diphenylacetylene Semi-Hydrogenation.
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- ChemCatChem, 2015, v. 7, n. 6, p. 952, doi. 10.1002/cctc.201402999
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Fluorescence emission, life time, thermal properties of trans-stilbene mixed diphenylacetylene scintillator crystal.
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- Journal of Materials Science: Materials in Electronics, 2021, v. 32, n. 7, p. 8366, doi. 10.1007/s10854-021-05421-8
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Simple Modifications for the Facile Preparation of 1,1,2,3,4,4‐Hexaaryl‐1,3‐butadienes.
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- Helvetica Chimica Acta, 2022, v. 105, n. 2, p. 1, doi. 10.1002/hlca.202100232
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1,3-Dipolar Cycloadditions of Ethyl 2-Diazo-3,3,3-trifluoropropanoate to Alkynes and [1,5] Sigmatropic Rearrangements of the Resulting 3 H-Pyrazoles: Synthesis of Mono-, Bis- and Tris(trifluoromethyl)-Substituted Pyrazoles.
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- Helvetica Chimica Acta, 2014, v. 97, n. 6, p. 808, doi. 10.1002/hlca.201400032
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Membrane activity of 3-hydroxyglutarate diesters.
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- Supramolecular Chemistry, 2012, v. 24, n. 1, p. 29, doi. 10.1080/10610278.2011.622382
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Annulation of m-Substituted Aromatic Ketones with Diphenylacetylene Catalyzed by Ruthenium: A Reliable Route to Substituted Naphthalene Derivatives.
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- Russian Journal of General Chemistry, 2022, v. 92, n. 12, p. 2899, doi. 10.1134/S107036322212043X
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Electrochemical Behaviors of Adenosine-5′-triphosphate on Molecular Wire Modified Carbon Paste Electrode and Its Sensitive Detection.
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- Journal of the Chinese Chemical Society, 2012, v. 59, n. 12, p. 1571, doi. 10.1002/jccs.201200179
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Synthesis and Optical Properties of Push-Push-Pull Chromophores Based on Imidazo[5,1,2-cd]indolizines and Naphtho[1',2':4,5]imidazo[1,2-a]pyridines.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 40, p. 5975, doi. 10.1002/ejoc.201701109
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Catalytic semi‐hydrogenation through hydrogen transfer from carbohydrates as a sustainable hydrogen source over bimetallic PdCuFe<sub>3</sub>O<sub>4</sub> nanoparticles.
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- Bulletin of the Korean Chemical Society, 2023, v. 44, n. 7, p. 600, doi. 10.1002/bkcs.12701
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Correlation of Rates of Solvolysis of Diphenylacetyl Chloride Using Extended Grunwald-Winstein Equation.
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- Bulletin of the Korean Chemical Society, 2015, v. 36, n. 10, p. 2429, doi. 10.1002/bkcs.10465
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Pd/Ag Nanoparticles Prepared in Ionic Liquids as Model Catalysts for the Hydrogenation of Diphenylacetylene.
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- Chemie Ingenieur Technik (CIT), 2022, v. 94, n. 3, p. 328, doi. 10.1002/cite.202100163
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Liquid-Phase Hydrogenation of Internal and Terminal Alkynes on Pd–Ag/Al<sub>2</sub>O<sub>3</sub> Catalyst.
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- Kinetics & Catalysis, 2019, v. 60, n. 5, p. 642, doi. 10.1134/S0023158419050069
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Highly Selective Pd-Cu/α-Al<sub>2</sub>O<sub>3</sub> Catalysts for Liquid-Phase Hydrogenation: The Influence of the Pd: Cu Ratio on the Structure and Catalytic Characteristics.
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- Kinetics & Catalysis, 2018, v. 59, n. 5, p. 601, doi. 10.1134/S0023158418050105
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Size effect of Pd nanoparticles in the selective liquid-phase hydrogenation of diphenylacetylene.
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- Kinetics & Catalysis, 2015, v. 56, n. 6, p. 733, doi. 10.1134/S0023158415060130
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Pd-Cu catalysts from acetate complexes in liquid-phase diphenylacetylene hydrogenation.
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- Kinetics & Catalysis, 2015, v. 56, n. 5, p. 591, doi. 10.1134/S0023158415050122
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Synthesis of Sterically Congested Polycyclic Aromatic Hydrocarbons: Rhodium(III)-Catalyzed Cascade Oxidative Annulation of Aryl Ketoximes with Diphenylacetylene by Sequential Cleavage of Multiple CH Bonds.
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- Advanced Synthesis & Catalysis, 2014, v. 356, n. 11/12, p. 2688, doi. 10.1002/adsc.201400292
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[2+2]-Photocycloadditions of 1,4-Naphthoquinone Under Batch and Continuous-Flow Conditions.
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- Molecules, 2024, v. 29, n. 24, p. 5920, doi. 10.3390/molecules29245920
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Redox-Dependent Conformational Switching of Diphenylacetylenes.
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- Molecules, 2014, v. 19, n. 8, p. 11316, doi. 10.3390/molecules190811316
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Radical Thiol-yne Chemistry on Diphenylacetylene: Selective and Quantitative Addition Enabling the Synthesis of Hyperbranched Poly(vinyl sulfide)s.
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- Macromolecular Rapid Communications, 2013, v. 34, n. 22, p. 1772, doi. 10.1002/marc.201300707
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Cycloaddition of Dialkylalumanyl Anion toward Unsaturated Hydrocarbons in (1+2) and (1+4) Modes.
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- Chemistry - A European Journal, 2020, v. 26, n. 10, p. 2174, doi. 10.1002/chem.201905830
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Mechanistic Study of Highly Efficient Direct 1,2‐Carboboration of Alkynes with 9‐Borafluorenes.
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- Chemistry - A European Journal, 2018, v. 24, n. 50, p. 13223, doi. 10.1002/chem.201801818
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Electronic anti‐injection effect for carbonyl in anchor group based on diphenylacetylene D<sub>2</sub>‐π‐A sensitizer in dye‐sensitized solar cells.
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- International Journal of Energy Research, 2021, v. 45, n. 2, p. 2766, doi. 10.1002/er.5969
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