About: Novel Hyperbranched Poly([1,2,3]-triazole)s Derived from AB2 Monomers by a 1,3-Dipolar Cycloaddition

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About: Novel Hyperbranched Poly([1,2,3]-triazole)s Derived from AB2 Monomers by a 1,3-Dipolar Cycloaddition Goto Sponge NotDistinct Permalink

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paper from 2004 with over 100 times cited

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2004 (fr) наукова стаття, опублікована в червні 2004 (uk) im Juni 2004 veröffentlichter wissenschaftlicher Artikel (de) paper from 2004 with over 100 times cited (en)
publication date	wds:Q57778069-31B05750-855A-4103-B197-8D1ECECD7461
publication date	2004-06-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q57778069-0a193812-4db6-cf1c-9367-944e670a8ec2 wds:Q57778069-20f89007-4ae2-e666-15d0-058c732ca7b1 wds:Q57778069-434fdf1b-462b-0c31-0899-fc272bee60d1 wds:Q57778069-47a3362e-4a3a-5f66-7833-d4942bfe1a2c wds:Q57778069-54ce1b80-4589-0e26-0a97-a5f0a69b5967 wds:Q57778069-61f00809-4488-25cd-440a-89da113bae82 wds:Q57778069-67a04af2-44d2-36c6-41eb-3129c53846f8 wds:Q57778069-8a002521-4e8f-cf6f-fb5f-78cf42510e3a wds:Q57778069-d353649a-43c3-bacc-9d15-b075cbeeeae6 wds:Q57778069-f5c34212-49b9-de0a-7403-839a7a88d182
cites work	A stepwise huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes Click Chemistry: Diverse Chemical Function from a Few Good Reactions An approach to hyperbranched polymers with a degree of branching of 100% Steric Effects on the Regioselectivity of an Azide-Alkyne Dipolar Cycloaddition Reaction: The Synthesis of Human Leukocyte Elastase Inhibitors New developments in hyperbranched polymers Azides: their preparation and synthetic uses Ab initio and experimental study on thermally degradable polycarbonates: the effect of substituents on the reaction rates Solid-phase synthesis of 1,2,3-triazoles via 1,3-dipolar cycloaddition Structure characterization of hyperbranched poly(ether amide)s: I. Preparative fractionation Labile hyperbranched poly(triazene ester)s - decomposition behavior and their use as porogens in thermally stable matrix polymers
rdfs:label	Novel Hyperbranched Poly([1,2,3]-triazole)s Derived from AB2 Monomers by a 1,3-Dipolar Cycloaddition (en) Novel Hyperbranched Poly([1,2,3]-triazole)s Derived from AB2 Monomers by a 1,3-Dipolar Cycloaddition (nl)
skos:prefLabel	Novel Hyperbranched Poly([1,2,3]-triazole)s Derived from AB2 Monomers by a 1,3-Dipolar Cycloaddition (en) Novel Hyperbranched Poly([1,2,3]-triazole)s Derived from AB2 Monomers by a 1,3-Dipolar Cycloaddition (nl)
name	Novel Hyperbranched Poly([1,2,3]-triazole)s Derived from AB2 Monomers by a 1,3-Dipolar Cycloaddition (en) Novel Hyperbranched Poly([1,2,3]-triazole)s Derived from AB2 Monomers by a 1,3-Dipolar Cycloaddition (nl)
author	wds:Q57778069-61783bb2-41d0-0b1f-e302-37f427a66180 wds:Q57778069-E64841BB-BBD7-4245-AF35-BA04BC11012C wds:Q57778069-eefeae32-4bbb-beb0-90ad-629d8c72bccc
author	Brigitte Voit Hartmut Komber Arnulf J. Scheel
title	wds:Q57778069-24A292A7-6B4F-4E3B-96EB-0C1960C698DF
title	Novel Hyperbranched Poly([1,2,3]-triazole)s Derived from AB2 Monomers by a 1,3-Dipolar Cycloaddition (en)
page(s)	wds:Q57778069-0955F476-8F03-4ACF-946C-39A49BAFAF21
page(s)	1175-1180
instance of	wds:Q57778069-BA6F8132-F4EB-49B6-9E25-1638BFD4FB98
instance of	scholarly article
main subject	wds:Q57778069-19B2658B-C123-4F4B-8EAD-3EB03573D577
main subject	cycloaddition
published in	wds:Q57778069-49E80376-A9A8-4A1D-9ACF-A209A4A72C0D
published in	Macromolecular Rapid Communications
issue	wds:Q57778069-836D7EB6-17DC-4125-B21D-5E5EE71ACB75
volume	wds:Q57778069-5F295E64-414E-48E3-ACE1-841FAAC2425D
issue	12
volume	25
DOI	wds:Q57778069-4EBDFCEB-2229-4C1C-A77B-4D34248D7967
DOI	http://dx.doi.org/10.1002/MARC.200400097
DOI	10.1002/MARC.200400097
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57778069
is cites work of	Hyperbranched and Highly Branched Polymer Architectures-Synthetic Strategies and Major Characterization Aspects The Rise of Azide–Alkyne 1,3-Dipolar 'Click' Cycloaddition and its Application to Polymer Science and Surface Modification Acetylenic polymers: syntheses, structures, and functions Click polymerization Click Chemistry: Versatility and Control in the Hands of Materials Scientists 'Click' Chemistry in Polymer and Materials Science Cycloaddition Reactions and Dendritic Polymer Architectures – A Perfect Match Diels-Alder "click" chemistry in designing dendritic macromolecules. Click-chemistry as an efficient synthetic tool for the preparation of novel conjugated polymers Clicking polymers: a straightforward approach to novel macromolecular architectures Hyperbranched polymers - All problems solved after 15 years of research? CuI-Catalyzed Alkyne-Azide “Click” Cycloadditions from a Mechanistic and Synthetic Perspective Efficient polymerization of azide and active internal alkynes. UCST Behavior of Cyclodextrin-Containing Poly(Pseudo-Betaines) Based on Supramolecular Structures Marrying click chemistry with polymerization: expanding the scope of polymeric materials 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. The potential of cycloaddition reactions in the synthesis of dendritic polymers Click Chemistry: Copper Clusters Catalyse the Cycloaddition of Azides with Terminal Alkynes 'Click' Chemistry in Polymer and Material Science: An Update Carboxylic acid functionalized fluorinated sulfonated poly(arylene ether sulfone) copolymers with enhanced oxidative stability Highly proton conducting fluorinated sulfonated poly(arylene ether sulfone) copolymers with side chain grafting New design strategies for second-order nonlinear optical polymers and dendrimers Click Polymerization: Progresses, Challenges, and Opportunities Kinetic Study of the Thermal Polymerization Reactions between Diazide and Internal Diyne Chain-growth click polymerization of AB2 monomers for the formation of hyperbranched polymers with low polydispersities in a one-pot process. The use of azide-alkyne click chemistry in recent syntheses and applications of polytriazole-based nanostructured polymers "Flash" solvent-free synthesis of triazoles using a supported catalyst. MALDI−TOF Mass Spectral Characterization of Polymers Containing an Azide Group: Evidence of Metastable Ions Combining Ring-Opening Metathesis Polymerization (ROMP) with Sharpless-Type 'Click' Reactions: An Easy Method for the Preparation of Side Chain Functionalized Poly(oxynorbornenes) Synthesis of Polyethers Containing Triazole Units in the Backbone by Click Chemistry in a Tricomponent Reaction Advances in cycloaddition polymerizations Catalyst-Free Thiol–Yne Click Polymerization: A Powerful and Facile Tool for Preparation of Functional Poly(vinylene sulfide)s Azide/Alkyne-'Click' Reactions: Applications in Material Science and Organic Synthesis Click polymerizations: Encouraging route for shape memory polymers Hyperbranched Poly(aroxycarbonyltriazole)s: Metal-Free Click Polymerization, Light Refraction, Aggregation-Induced Emission, Explosive Detection, and Fluorescent Patterning Hyperbranched polymer architectures: From Flory's AB(f-1) polycondensates to controlled structures One-Pot Synthesis of Polypyrazoles by Click Reactions Metal- and solvent-free, clickable synthesis and postpolymerization functionalization of poly(triazole)s Hydroquinone Based Sulfonated Copolytriazoles with Enhanced Proton Conductivity Sulfonated polytriazoles from a new fluorinated diazide monomer and investigation of their proton exchange properties Phenol-yne Click Polymerization: An Efficient Technique to Facilely Access Regio- and Stereoregular Poly(vinylene ether ketone)s. Original Fluorinated Copolymers Achieved by Both Azide/Alkyne 'Click' Reaction and Hay Coupling from Tetrafluoroethylene Telomers

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