Novel Hyperbranched Poly([1,2,3]-triazole)s Derived from AB2 Monomers by a 1,3-Dipolar Cycloaddition
about
Vegetable oil derived solvent, and catalyst free "click chemistry" thermoplastic polytriazolesMALDI−TOF Mass Spectral Characterization of Polymers Containing an Azide Group: Evidence of Metastable IonsAcetylenic polymers: syntheses, structures, and functions"Flash" solvent-free synthesis of triazoles using a supported catalyst.Click-chemistry as an efficient synthetic tool for the preparation of novel conjugated polymers.Advances in cycloaddition polymerizations.Clicking polymers: a straightforward approach to novel macromolecular architectures.Marrying click chemistry with polymerization: expanding the scope of polymeric materials.Click polymerization.One-Pot Synthesis of Polypyrazoles by Click ReactionsPhenol-yne Click Polymerization: An Efficient Technique to Facilely Access Regio- and Stereoregular Poly(vinylene ether ketone)s.Diels-Alder "click" chemistry in designing dendritic macromolecules.Metal-Free Poly-Cycloaddition of Activated Azide and Alkynes toward Multifunctional Polytriazoles: Aggregation-Induced Emission, Explosive Detection, Fluorescent Patterning, and Light Refraction.A series of hyperbranched polytriazoles containing perfluoroaromatic rings from AB2-type monomers: convenient syntheses by click chemistry under copper(I) catalysis and enhanced optical nonlinearity.Chain-growth click polymerization of AB2 monomers for the formation of hyperbranched polymers with low polydispersities in a one-pot process.Efficient polymerization of azide and active internal alkynes.The Rise of Azide–Alkyne 1,3-Dipolar 'Click' Cycloaddition and its Application to Polymer Science and Surface ModificationCuI-Catalyzed Alkyne-Azide “Click” Cycloadditions from a Mechanistic and Synthetic PerspectiveMetal- and solvent-free, clickable synthesis and postpolymerization functionalization of poly(triazole)sUCST Behavior of Cyclodextrin-Containing Poly(Pseudo-Betaines) Based on Supramolecular StructuresClick Chemistry: Versatility and Control in the Hands of Materials ScientistsHydroquinone Based Sulfonated Copolytriazoles with Enhanced Proton ConductivityCarboxylic acid functionalized fluorinated sulfonated poly(arylene ether sulfone) copolymers with enhanced oxidative stabilityHighly proton conducting fluorinated sulfonated poly(arylene ether sulfone) copolymers with side chain graftingSulfonated polytriazoles from a new fluorinated diazide monomer and investigation of their proton exchange propertiesHyperbranched and Highly Branched Polymer Architectures-Synthetic Strategies and Major Characterization AspectsCycloaddition Reactions and Dendritic Polymer Architectures – A Perfect MatchThe potential of cycloaddition reactions in the synthesis of dendritic polymersHyperbranched polymers - All problems solved after 15 years of research?Biological evaluation of 1,2,3-triazole-based polymers for potential applications as hard tissue materialSynthesis of Polyethers Containing Triazole Units in the Backbone by Click Chemistry in a Tricomponent ReactionCatalyst-Free Thiol–Yne Click Polymerization: A Powerful and Facile Tool for Preparation of Functional Poly(vinylene sulfide)sSynthesis and Characterization of Highly Proton Conducting Sulfonated PolytriazolesClick Chemistry: Copper Clusters Catalyse the Cycloaddition of Azides with Terminal AlkynesClick Polymerization: Progresses, Challenges, and Opportunities'Click' Chemistry in Polymer and Materials ScienceDesign a Highly Reactive Trifunctional Core Molecule To Obtain Hyperbranched Polymers with over a Million Molecular Weight in One-Pot Click Polymerization'Click' Chemistry in Polymer and Material Science: An UpdateAzide/Alkyne-'Click' Reactions: Applications in Material Science and Organic SynthesisCombining Ring-Opening Metathesis Polymerization (ROMP) with Sharpless-Type 'Click' Reactions: An Easy Method for the Preparation of Side Chain Functionalized Poly(oxynorbornenes)
P2860
Q21284524-097D23BC-4CB3-4F6F-BC07-E6A5E0744B22Q24604090-591161ea-4eda-cf93-5e2d-40b72c5b2ce0Q28254863-03fe4154-486b-5496-31b7-1c7062e9630aQ33402886-B270A717-88AC-436C-8CDE-3CD1CA452F16Q34444594-271217ea-4a4a-2d12-4afe-646c0530b2c9Q36408503-3F48D65D-67DB-4063-BCE2-3F643688D654Q36874115-1075ba15-4d07-06b6-70cf-acbb20d1a56eQ37716662-b932fca2-4ffe-1d51-a2c4-d4d12ced8655Q37767149-ec71514f-4555-967b-fbd4-98bdf69f5125Q42111142-80009CB9-283E-40B7-82C6-6C426896B26DQ47965526-35F14108-C4AA-469E-B5BB-9029B896E22DQ50594970-7a056622-44ae-82b1-a36b-eb5799f38d1aQ50879976-E549C264-7414-4FE9-89F6-036432F64EE9Q51537647-185721F5-D566-4AE0-9792-F20201549D06Q53465117-F0371CD1-88FE-46C0-A0C3-9459E682084CQ53744347-4EB760F6-B9CA-4190-8BB7-3F79964BCB9CQ56566537-ad342944-4be2-84e9-9233-823e9cf75aebQ56566542-4cbb3553-48f6-1764-ac74-b2ee9cab164aQ57344611-A851A7F6-9C93-453A-9D22-0EF26CBC905AQ57349392-C4DC9180-1D15-424D-BE40-1935584477A0Q57350000-6499fc31-4331-2b14-f2ed-95e729b37a40Q57776804-B94D2740-86E2-4BB2-8950-F72F9DEA942BQ57776874-b23f8ac1-45fa-e0f6-7d42-28375a255502Q57777135-ACE513C3-FD03-4AB1-8A36-A1C1DA877837Q57777185-2c63f85f-4c46-de04-697e-38e357bb027fQ57777608-4f3a9aa2-42e7-13a6-e32a-3236d5db0f02Q57777734-0efada2d-42a9-b732-2981-9c9770bccccfQ57777805-F2B30208-EAD6-48A3-9AEB-A5561D591A18Q57777961-98e4a44b-4e23-febc-b942-bd849dc1a1b7Q58383842-2CFC8F2A-B978-497C-8AEE-244D12BE8FCDQ59020249-6E6D052D-ED9A-4F20-B49A-4D7541C44DCDQ60020510-3d11bc1f-4df1-22f6-1c25-a4681975fd12Q65807649-d54ccade-4d57-0a9e-1fdd-82ca8db9c583Q66422618-123199eb-4180-3573-4d7d-9dcd7a3441a3Q66422754-cce703c0-427c-1bda-a8f5-aa320d52f73cQ66816557-8200f11c-4f3d-cbae-c124-d078e674d319Q67840244-cf0227cb-4b49-43f1-974e-cf1b4f93b255Q69259965-2c3e78ed-4b17-5c9f-1814-de5d59d77beaQ69261311-28c97a41-4ea1-6eb7-ca89-f7a70cb91e53Q69262981-97c07d05-4af2-0315-5847-894a7c0fa675
P2860
Novel Hyperbranched Poly([1,2,3]-triazole)s Derived from AB2 Monomers by a 1,3-Dipolar Cycloaddition
description
im Juni 2004 veröffentlichter wissenschaftlicher Artikel
@de
paper from 2004 with over 100 times cited
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в червні 2004
@uk
name
Novel Hyperbranched Poly([1,2, ...... by a 1,3-Dipolar Cycloaddition
@en
Novel Hyperbranched Poly([1,2, ...... by a 1,3-Dipolar Cycloaddition
@nl
type
label
Novel Hyperbranched Poly([1,2, ...... by a 1,3-Dipolar Cycloaddition
@en
Novel Hyperbranched Poly([1,2, ...... by a 1,3-Dipolar Cycloaddition
@nl
prefLabel
Novel Hyperbranched Poly([1,2, ...... by a 1,3-Dipolar Cycloaddition
@en
Novel Hyperbranched Poly([1,2, ...... by a 1,3-Dipolar Cycloaddition
@nl
P2860
P50
P356
P1476
Novel Hyperbranched Poly([1,2, ...... by a 1,3-Dipolar Cycloaddition
@en
P2860
P304
P356
10.1002/MARC.200400097
P577
2004-06-01T00:00:00Z