Works matching DE "TRIPTYCENES"
Results: 88
Cover Feature: Intramolecular Hiyama Coupling: Synthesis of 1,8,13‐Trisubstituted Chiral Triptycenes with Three Different Substituents by Intramolecular Substituent Transfer (Chem. Eur. J. 39/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 39, p. 1, doi. 10.1002/chem.202301655
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Intramolecular Hiyama Coupling: Synthesis of 1,8,13‐Trisubstituted Chiral Triptycenes with Three Different Substituents by Intramolecular Substituent Transfer.
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- Chemistry - A European Journal, 2023, v. 29, n. 39, p. 1, doi. 10.1002/chem.202300988
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Ultrapermeable Polymers of Intrinsic Microporosity Containing Spirocyclic Units with Fused Triptycenes.
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- Advanced Functional Materials, 2021, v. 31, n. 37, p. 1, doi. 10.1002/adfm.202104474
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Synthesis of soluble and thermally stable triptycene-based poly(amide-imide)s.
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- Journal of Polymer Research, 2014, v. 21, n. 3, p. 1, doi. 10.1007/s10965-014-0391-x
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Synthesis and characterization of novel organosoluble and thermally stable polyamides bearing triptycene in their backbones.
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- Journal of Polymer Research, 2012, v. 19, n. 7, p. 1, doi. 10.1007/s10965-012-9902-9
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Triptycene poly(ether-imide)s with high solubility and optical transparency.
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- Journal of Polymer Research, 2012, v. 19, n. 1, p. 1, doi. 10.1007/s10965-011-9757-5
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Guest-dependent complexation of triptycene-derived macrotricyclic host containing one anthracene moiety with paraquat derivatives: construction of [2]rotaxanes.
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- Supramolecular Chemistry, 2015, v. 27, n. 5/6, p. 357, doi. 10.1080/10610278.2014.976220
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Templated growth of fullerene C 60 crystals by triptycene in polymer blend films.
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- Supramolecular Chemistry, 2012, v. 24, n. 7, p. 526, doi. 10.1080/10610278.2012.691607
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A Triptycene-Based Porous Organic Polymer that Exhibited High Hydrogen and Carbon Dioxide Storage Capacities and Excellent CO<sub>2</sub>/N<sub>2</sub> Selectivity.
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- Chinese Journal of Chemistry, 2015, v. 33, n. 5, p. 539, doi. 10.1002/cjoc.201500181
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Complexation of Triptycene-Derived Macrotricyclic Host Containing Pyridine Groups with Paraquat Derivatives: A Switchable Process Controlled by Zn<sup>2+</sup> Ions.
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- Chinese Journal of Chemistry, 2014, v. 32, n. 8, p. 721, doi. 10.1002/cjoc.201400400
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High Thermally Stable and Organosoluble New Poly(amide-imide)s Derived from Bis(4-trimellitimido phenoxy)phenyl Triptycene.
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- Journal of Macromolecular Science: Physics, 2015, v. 54, n. 6, p. 749, doi. 10.1080/00222348.2015.1037216
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Facile Synthesis of Triptycene‐Azolium Salts and NHC‐Metal Complexes.
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- European Journal of Inorganic Chemistry, 2023, v. 26, n. 18, p. 1, doi. 10.1002/ejic.202300178
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Synthesis and study of new poly(ester-imide)s containing triptycene groups.
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- Polymer Engineering & Science, 2014, v. 54, n. 10, p. 2252, doi. 10.1002/pen.23780
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Ultrafast Energy Transfer in Triptycene-Grafted Bodipy Scaffoldings.
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- Chemistry - A European Journal, 2013, v. 19, n. 27, p. 8900, doi. 10.1002/chem.201300413
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离子液体修饰的三蝶烯多孔材料用于 去除水溶液中阴离子染料.
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- Journal of East China University of Science & Technology, 2020, v. 46, n. 2, p. 155, doi. 10.14135/j.cnki.1006-3080.20190104001
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Chiral Iodotriptycenes: Synthesis and Catalytic Applications Front Cover: (ChemistryOpen 8/2022).
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- ChemistryOpen, 2022, v. 11, n. 8, p. 1, doi. 10.1002/open.202200159
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Chiral Iodotriptycenes: Synthesis and Catalytic Applications.
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- ChemistryOpen, 2022, v. 11, n. 8, p. 1, doi. 10.1002/open.202200158
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Chiral Iodotriptycenes: Synthesis and Catalytic Applications.
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- ChemistryOpen, 2022, v. 11, n. 7, p. 1, doi. 10.1002/open.202200145
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Preparation of Tri- and Hexasubstituted Triptycene Synthons by Transition Metal Catalyzed Cross-Coupling Reactions for Post-Modifications.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 1, p. 185, doi. 10.1002/ejoc.201501272
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Linker-Length-Dependent Complexation of a Triptycene-Derived Macrotricyclic Polyether with π-Extended Viologens.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 6, p. 1257, doi. 10.1002/ejoc.201403390
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Synthesis and Reactions of Triptycene-Derived Bromocalix[5]arenes: Conformational Transformation from Cone to 1,2-Alternate.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 9, p. 1976, doi. 10.1002/ejoc.201301668
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Pushing the Lewis Acidity Boundaries of Boron Compounds With Non‐Planar Triarylboranes Derived from Triptycenes.
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- Angewandte Chemie, 2019, v. 131, n. 47, p. 17045, doi. 10.1002/ange.201910908
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Interpenetration Isomerism in Triptycene‐Based Hydrogen‐Bonded Organic Frameworks.
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- Angewandte Chemie, 2019, v. 131, n. 6, p. 1678, doi. 10.1002/ange.201811263
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Blurring the Lines between Host and Guest: A Chimeric Receptor Derived from Cucurbituril and Triptycene.
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- Angewandte Chemie, 2018, v. 130, n. 27, p. 8205, doi. 10.1002/ange.201803132
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Regioselective One-Pot Synthesis of Triptycenes via Triple-Cycloadditions of Arynes to Ynolates.
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- Angewandte Chemie, 2017, v. 129, n. 5, p. 1318, doi. 10.1002/ange.201609111
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A Conformationally Stable Contorted Hexabenzoovalene.
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- Angewandte Chemie, 2016, v. 128, n. 50, p. 15823, doi. 10.1002/ange.201607740
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Modulation of the E. coli rpoH Temperature Sensor with Triptycene- Based Small Molecules.
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- Angewandte Chemie, 2016, v. 128, n. 29, p. 8398, doi. 10.1002/ange.201601626
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Triptycene-Based Chiral Macrocyclic Hosts for Highly Enantioselective Recognition of Chiral Guests Containing a Trimethylamino Group.
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- Angewandte Chemie, 2016, v. 128, n. 17, p. 5390, doi. 10.1002/ange.201600911
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The HOMO Nodal Arrangement in Polychromophoric Molecules and Assemblies Controls the Interchromophoric Electronic Coupling.
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- Angewandte Chemie, 2015, v. 127, n. 48, p. 14676, doi. 10.1002/ange.201506402
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Recognition of Nucleic Acid Junctions Using Triptycene-Based Molecules.
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- Angewandte Chemie, 2014, v. 126, n. 50, p. 13966, doi. 10.1002/ange.201407061
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Binding and interaction of di- and tri-substituted organometallic triptycene palladium complexes with DNA.
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- Journal of Biological Inorganic Chemistry (JBIC), 2014, v. 19, n. 7, p. 1221, doi. 10.1007/s00775-014-1180-z
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Optically transparent, organosoluble poly(ether-amide)s bearing triptycene unit; synthesis and characterization.
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- Journal of Macromolecular Science: Pure & Applied Chemistry, 2018, v. 55, n. 9, p. 658, doi. 10.1080/10601325.2018.1510291
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Palladium‐Catalyzed α‐Selective Halogenation of Triptycene Using Sulfur Directing Group.
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- Asian Journal of Organic Chemistry, 2023, v. 12, n. 12, p. 1, doi. 10.1002/ajoc.202300588
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Microwave‐Assisted [4+2] Diels–Alder Cycloaddition of 1,4‐Diethynyl Triptycene with Various Cyclopentadienone Derivatives: Promising Building Blocks for Polymer Networks.
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- Asian Journal of Organic Chemistry, 2018, v. 7, n. 2, p. 378, doi. 10.1002/ajoc.201700655
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Fluoride Anion Complexation by a Triptycene-Based Distiborane: Taking Advantage of a Weak but Observable C−H⋅⋅⋅F Interaction.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 7, p. 1799, doi. 10.1002/anie.201611009
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Regioselective One-Pot Synthesis of Triptycenes via Triple-Cycloadditions of Arynes to Ynolates.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 5, p. 1298, doi. 10.1002/anie.201609111
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- Article
A Conformationally Stable Contorted Hexabenzoovalene.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 50, p. 15594, doi. 10.1002/anie.201607740
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- Article
Triptycene-Based Chiral Macrocyclic Hosts for Highly Enantioselective Recognition of Chiral Guests Containing a Trimethylamino Group.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 17, p. 5304, doi. 10.1002/anie.201600911
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Recognition of Nucleic Acid Junctions Using Triptycene-Based Molecules.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 50, p. 13746, doi. 10.1002/anie.201407061
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A Permanent Mesoporous Organic Cage with an Exceptionally High Surface Area.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 6, p. 1516, doi. 10.1002/anie.201308924
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Triptycene‐based fluorescent polymers with pendant alkyl chains: interaction with fullerenes and morphology of thin films.
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- Polymer International, 2019, v. 68, n. 3, p. 481, doi. 10.1002/pi.5737
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Preparation and characterization of heat-resistant polyimide/titanium dioxide nanocomposite films containing triptycene side units by sol–gel processes.
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- High Performance Polymers, 2014, v. 26, n. 4, p. 373, doi. 10.1177/0954008313515285
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Cover Feature: Azobenzene‐Substituted Triptycenes: Understanding the Exciton Coupling of Molecular Switches in Close Proximity (Chem. Eur. J. 38/2022).
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- Chemistry - A European Journal, 2022, v. 28, n. 38, p. 1, doi. 10.1002/chem.202201762
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Azobenzene‐Substituted Triptycenes: Understanding the Exciton Coupling of Molecular Switches in Close Proximity.
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- Chemistry - A European Journal, 2022, v. 28, n. 38, p. 1, doi. 10.1002/chem.202200972
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Retro‐Friedel–Crafts‐Type Acidic Ring‐Opening of Triptycenes: A New Synthetic Approach to Acenes.
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- Chemistry - A European Journal, 2022, v. 28, n. 12, p. 1, doi. 10.1002/chem.202104160
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Front Cover: Retro‐Friedel‐Crafts‐Type Acidic Ring‐Opening of Triptycenes: A New Synthetic Approach to Acenes (Chem. Eur. J. 12/2022).
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- Chemistry - A European Journal, 2022, v. 28, n. 12, p. 1, doi. 10.1002/chem.202200415
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Retro‐Friedel‐Crafts‐Type Acidic Ring‐Opening of Triptycenes: A New Synthetic Approach to Acenes.
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- Chemistry - A European Journal, 2022, v. 28, n. 12, p. 1, doi. 10.1002/chem.202104160
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Cover Feature: Quadruple Role of Pd Catalyst in Domino Reaction Involving Aryl to Alkyl 1,5‐Pd Migration to Access 1,9‐Bridged Triptycenes (Chem. Eur. J. 45/2021).
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- Chemistry - A European Journal, 2021, v. 27, n. 45, p. 11478, doi. 10.1002/chem.202102468
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Quadruple Role of Pd Catalyst in Domino Reaction Involving Aryl to Alkyl 1,5‐Pd Migration to Access 1,9‐Bridged Triptycenes.
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- Chemistry - A European Journal, 2021, v. 27, n. 45, p. 11548, doi. 10.1002/chem.202101728
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Frontispiece: Chiral Triptycenes: Concepts, Progress and Prospects.
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- Chemistry - A European Journal, 2021, v. 27, n. 24, p. 1, doi. 10.1002/chem.202182463
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