Works matching Cyano group
Results: 856
侧氰基芳醚硅芳炔树脂的制备与表征.
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- Acta Materiae Compositae Sinica, 2020, v. 37, n. 12, p. 3035, doi. 10.13801/j.cnki.fhclxb.20200507.003
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Enhanced properties of poly(silylene phenylether arylacetylene) by a side cyano group.
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- Polymer Engineering & Science, 2022, v. 62, n. 9, p. 2900, doi. 10.1002/pen.26071
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Amorphous Carbon and Cyano-Group Self-Modified P-Doped g-C 3 N 4 for Boosting Photocatalytic H 2 Evolution.
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- Catalysts (2073-4344), 2024, v. 14, n. 8, p. 523, doi. 10.3390/catal14080523
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Cyano/Hydroxyl Groups Co-Functionalized g-C 3 N 4 for Photocatalytic NO Removal: A Synergistic Strategy towards Inhibition of Toxic Intermediate NO 2.
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- Catalysts (2073-4344), 2023, v. 13, n. 11, p. 1433, doi. 10.3390/catal13111433
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Synergy of Iron Doping and Cyano Groups for Enhanced Photocatalytic Hydrogen Production over C<sub>3</sub>N<sub>4</sub>.
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- Chemistry - A European Journal, 2021, v. 27, n. 70, p. 17628, doi. 10.1002/chem.202103092
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Highly Stable Perovskite Solar Cells Based on the Efficient Interaction between Pb<sup>2+</sup> and Cyano Groups of 4‐Aminophthalonitrile.
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- Chemistry - A European Journal, 2023, v. 29, n. 71, p. 1, doi. 10.1002/chem.202302703
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Vacuum pyrolysis of polymeric wastes containing hazardous cyano groups.
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- Journal of Material Cycles & Waste Management, 2013, v. 15, n. 2, p. 218, doi. 10.1007/s10163-012-0113-6
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The Performance and Synthesis of Alkynyl−Functionalized Benzoxazine Containing Phthalide Side Groups and Cyano Groups with Different Molecular Weights.
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- Polymers (20734360), 2023, v. 15, n. 16, p. 3478, doi. 10.3390/polym15163478
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Synthesis and properties of benzocyclobutene-terminated imide-containing cyano group.
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- High Performance Polymers, 2019, v. 31, n. 9/10, p. 1062, doi. 10.1177/0954008318821710
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Photothermal-Assisted Photocatalytic Degradation of Tetracycline in Seawater Based on the Black g-C 3 N 4 Nanosheets with Cyano Group Defects.
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- Catalysts (2073-4344), 2023, v. 13, n. 7, p. 1147, doi. 10.3390/catal13071147
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Polynuclear Aromatic Amines as N-Nucleophiles in the ipso-Substitution of the Cyano Group in 1,2,4-Triazines.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 2, p. 335, doi. 10.1134/S1070428020010268
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Potassium‐Ion‐Assisted Regeneration of Active Cyano Groups in Carbon Nitride Nanoribbons: Visible‐Light‐Driven Photocatalytic Nitrogen Reduction.
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- Angewandte Chemie, 2019, v. 131, n. 46, p. 16797, doi. 10.1002/ange.201908640
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New soluble polyamides and polyimides containing polar functional groups: pendent pyrazole rings with amino and cyano groups.
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- Designed Monomers & Polymers, 2016, v. 19, n. 3, p. 227, doi. 10.1080/15685551.2015.1136529
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Intramolecular Reaction of tert‐Butyl‐NNO‐Azoxy and Cyano Groups – Novel Synthesis of Pyridazine, 1,2,3‐Triazepine, and Furan Rings.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 43, p. 5947, doi. 10.1002/ejoc.201800947
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Versatility of the Cyano Group in Intermolecular Interactions.
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- Molecules, 2020, v. 25, n. 19, p. 4495, doi. 10.3390/molecules25194495
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Stepwise Introduction of Cyano Groups into <italic>nido</italic>‐ and <italic>closo</italic>‐Undecaborate Clusters.
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- Chemistry - A European Journal, 2018, v. 24, n. 14, p. 3528, doi. 10.1002/chem.201704860
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Synthesis and properties of bismaleimide resins containing phthalide cardo and cyano groups.
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- High Performance Polymers, 2019, v. 31, n. 4, p. 462, doi. 10.1177/0954008318782342
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Activation of the Cyano Group at Imidazole via Copper Stimulated Alcoholysis.
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- Inorganics, 2019, v. 7, n. 7, p. 87, doi. 10.3390/inorganics7070087
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A review of the synthesis and coordination of some lesser studied thiourea ligands bearing electronegative sulfonyl, phosphoryl and cyano substituents towards platinum group and related metal centers.
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- Journal of Coordination Chemistry, 2024, v. 77, n. 15/16, p. 1679, doi. 10.1080/00958972.2024.2407665
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Computational and experimental investigations of a cyano group containing novel small molecule organic semiconductor.
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- Journal of Materials Science: Materials in Electronics, 2021, v. 32, n. 11, p. 14749, doi. 10.1007/s10854-021-06030-1
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Synthesis of a Cyclophosphazene Derivative Containing Multiple Cyano Groups for Electron-Beam Irradiated Flame-Retardant Materials.
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- Polymers (20734360), 2021, v. 13, n. 20, p. 3460, doi. 10.3390/polym13203460
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Enhancing Effects of the Cyano Group on the C-X∙∙∙N Hydrogen or Halogen Bond in Complexes of X-Cyanomethanes with Trimethyl Amine: CH 3−n (CN) n X∙∙∙NMe 3 , (n = 0–3; X = H, Cl, Br, I).
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- International Journal of Molecular Sciences, 2022, v. 23, n. 19, p. 11289, doi. 10.3390/ijms231911289
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Step-by-Step Replacement of Cyano Groups by Tricyanovinyls—The Influence on the Acidity.
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- Molecules, 2023, v. 28, n. 24, p. 8157, doi. 10.3390/molecules28248157
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Synthesis and characterization of poly(ether ketone ether ketone ketone)/poly(ether ether ketone ketone) copolymers containing naphthalene and pendant cyano groups.
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- Journal of Applied Polymer Science, 2009, v. 112, n. 6, p. 3225, doi. 10.1002/app.29792
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The Cyano Group as a Traceless Activation Group for the Intermolecular [3+2] Cycloaddition of Azomethine Ylides: A Five-Step Synthesis of (±)-Isoretronecanol.
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- Angewandte Chemie, 2015, v. 127, n. 21, p. 6404, doi. 10.1002/ange.201500961
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Integrated Cyano Groups into the Skeleton of Conjugated Polymers to Activate Molecular Oxygen for Boosting Photocatalytic H<sub>2</sub>O<sub>2</sub> Efficiency.
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- ChemSusChem, 2025, v. 18, n. 1, p. 1, doi. 10.1002/cssc.202400771
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Synthesis and properties of cyano group-containing polyimides with high peel strength.
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- High Performance Polymers, 2016, v. 28, n. 8, p. 953, doi. 10.1177/0954008315611469
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The Cyano Group as a Traceless Activation Group for the Intermolecular [3+2] Cycloaddition of Azomethine Ylides: A Five-Step Synthesis of (±)-Isoretronecanol.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 21, p. 6306, doi. 10.1002/anie.201500961
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Natural Abundance Nitrogen-15 NMR in Thermotropic Liquid Crystals With Cyano-Group.
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- Zeitschrift für Physikalische Chemie, 2017, v. 231, n. 4, p. 795, doi. 10.1515/zpch-2016-0814
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A Novel Strategy of In Situ Trimerization of Cyano Groups Between the Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub> (MXene) Interlayers for High-Energy and High-Power Sodium-Ion Capacitors.
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- Nano-Micro Letters, 2020, v. 12, n. 1, p. N.PAG, doi. 10.1007/s40820-020-00473-7
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Dipolar Dyes with a Pyrrolo[2,3- b]quinoxaline Skeleton Containing a Cyano Group and a Bridged Tertiary Amino Group: Synthesis, Solvatofluorochromism, and Bioimaging.
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- Chemistry - An Asian Journal, 2016, v. 11, n. 11, p. 1718, doi. 10.1002/asia.201600257
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Investigation of the curing mechanism and properties of bismaleimide‐triazine resins containing phenolphthalein and cyano group.
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- Journal of Applied Polymer Science, 2019, v. 136, n. 18, p. N.PAG, doi. 10.1002/app.47420
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Zinc-Catalyzed Direct Cyanation of Indoles and Pyrroles: Nitromethane as a Source of a Cyano Group.
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- Advanced Synthesis & Catalysis, 2014, v. 356, n. 2/3, p. 347, doi. 10.1002/adsc.201301073
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Substitution of Cyano Group in Position 5 of 1,2,4-Triazines by Carboxylic Acid Hydrazide Residues under Solvent-Free Conditions.
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- Russian Journal of Organic Chemistry, 2018, v. 54, n. 3, p. 509, doi. 10.1134/S1070428018030223
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Short communication Scandium(III) Triflate Catalyzed 1,4-Addition of Cyano Group to Enones Using Tetraethylammonium Cyanide as the Cyanide Source.
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- Acta Chimica Slovenica, 2013, v. 60, n. 3, p. 689
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Amplified Performance of Charge Accumulation and Trapping Induced by Enhancing the Dielectric Constant via the Cyano Group of 3D‐Structured Textile for a Triboelectric Multi‐Modal Sensor.
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- Small Methods, 2023, v. 7, n. 10, p. 1, doi. 10.1002/smtd.202300344
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Tuning the Properties of Graphdiyne by Introducing Electron‐Withdrawing/Donating Groups.
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- Angewandte Chemie, 2020, v. 132, n. 32, p. 13644, doi. 10.1002/ange.202004454
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One‐Step Realization of Crystallization and Cyano‐Group Generation for g‐C<sub>3</sub>N<sub>4</sub> Photocatalysts with Improved H<sub>2</sub> Production.
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- Solar RRL, 2021, v. 5, n. 2, p. 1, doi. 10.1002/solr.202000372
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Synthesis of Aromatic Nitriles Using Nonmetallic Cyano-Group Sources.
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- Angewandte Chemie International Edition, 2012, v. 51, n. 48, p. 11948, doi. 10.1002/anie.201206168
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侧向氟取代三环双酯氰基液晶的合成与性能研究.
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- Chinese Journal of Liquid Crystal & Displays, 2015, v. 30, n. 4, p. 559, doi. 10.3788/YJYXS20153004.0559
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Cyano group‐containing DOPO derivative for improving the flame retardancy, smoke suppression, and mechanical properties of epoxy resins.
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- Journal of Applied Polymer Science, 2024, v. 141, n. 28, p. 1, doi. 10.1002/app.55633
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Interaction of 2-Amino-(4-aryl)-Substituted Thia- and Oxazoles with 5-Cyano-1,2,4-triazines.
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- Doklady Chemistry, 2023, v. 508, n. 1, p. 28, doi. 10.1134/S0012500823600153
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Electrochemical Formation of Ionic Porous Organic Polymers Based on Viologen for Electrochromic Applications.
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- Macromolecular Rapid Communications, 2024, v. 45, n. 13, p. 1, doi. 10.1002/marc.202400031
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Synthesis of 5-[(Thiophen-3-yl)amino]-1,2,4-triazines.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 4, p. 675, doi. 10.1134/S1070428021040278
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Generation of New Synthons for Synthesis Through Activation of Nitromethane.
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- ChemSusChem, 2024, v. 17, n. 19, p. 1, doi. 10.1002/cssc.202400454
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Rational Design of Vinylene‐Linked Covalent Organic Frameworks for Modulating Photocatalytic H<sub>2</sub> Evolution.
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- ChemSusChem, 2023, v. 16, n. 20, p. 1, doi. 10.1002/cssc.202300872
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NaSCN‐Induced Cyano‐Rich Porous Graphitic Carbon Nitride with Sodium Dopant and Nitrogen Vacancies for Enhanced Photosynthesis of Hydrogen Peroxide.
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- Advanced Sustainable Systems, 2024, v. 8, n. 10, p. 1, doi. 10.1002/adsu.202400262
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Interaction of 2-Amino-1,3,4-thiadiazoles with 1,2,4-Triazine-5-carbonitriles.
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- Doklady Chemistry, 2022, v. 504, n. 1, p. 79, doi. 10.1134/S0012500822600146
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Synthesis of Polyfunctionalized [1,2′-Bipyridin]-1-ium Chlorides.
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- Russian Journal of Organic Chemistry, 2024, v. 60, n. 10, p. 2040, doi. 10.1134/S1070428024100221
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One-Pot Synthesis of 3-Carbamoyl-2-oxo-1,2-dihydropyridine-4-carboxylic Acids.
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- Russian Journal of Organic Chemistry, 2023, v. 59, n. 3, p. 536, doi. 10.1134/S1070428023030223
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