Hyperbranched polymers by thiol-yne chemistry: from small molecules to functional polymers.
about
Experimental and theoretical studies of scaling of sizes and intrinsic viscosity of hyperbranched chains in good solvents.Synthesis of a library of propargylated and PEGylated α-hydroxy acids toward "clickable" polylactides via hydrolysis of cyanohydrin derivatives.Photogenerated lectin sensors produced by thiol-ene/yne photo-click chemistry in aqueous solutionGrowing hyperbranched polymers using natural sunlightSynthesis of cyclic, multivalent Arg-Gly-Asp using sequential thiol-ene/thiol-yne photoreactions.Combining RAFT radical polymerization and click/highly efficient coupling chemistries: a powerful strategy for the preparation of novel materials."Clicking" on/with polymers: a rapidly expanding field for the straightforward preparation of novel macromolecular architectures.Synthesis and post-polymerisation modifications of aliphatic poly(carbonate)s prepared by ring-opening polymerisation.Post-functionalization of polymers via orthogonal ligation chemistry.Hyperbranched polymers: advances from synthesis to applications.Facile functionalization of polyesters through thiol-yne chemistry for the design of degradable, cell-penetrating and gene delivery dual-functional agents.AuICl-bound N-heterocyclic carbene ligands form MII4(LAuCl)6 integrally gilded cages.Visible light mediated metal-free thiol-yne click reaction.Janus cyclic peptide-polymer nanotubes.Quadrangular prism: a unique self-assembly from amphiphilic hyperbranched PMA-b-PAA.Rapid access to phospholipid analogs using thiol-yne chemistry.Radical thiol-yne chemistry on diphenylacetylene: selective and quantitative addition enabling the synthesis of hyperbranched poly(vinyl sulfide)s.Mechanism of the palladium-catalyzed hydrothiolation of alkynes to thioethers: a DFT study.Theoretical investigation of the impact of ligands on the regiodivergent Rh-catalyzed hydrothiolation of allyl amines.Cu0-Loaded organo-montmorillonite with improved affinity towards hydrogen: an insight into matrix-metal and non-contact hydrogen-metal interactions.Thioether-Bearing Hyperbranched Polyether Polyols with Methionine-Like Side-Chains: A Versatile Platform for Orthogonal Functionalization.Study of (Cyclic Peptide)-Polymer Conjugate Assemblies by Small-Angle Neutron Scattering.Facile Synthesis of DendriMac Polymers via the Combination of Living Anionic Polymerization and Highly Efficient Coupling Reactions.Synthesis and self-assembly behavior of POSS-embedded hyperbranched polymers.Combining ring-opening metathesis polymerization and thiol-ene coupling chemistries: facile access to novel functional linear and nonlinear macromolecules.Convenient synthesis of functionalized bis-ureidopyrimidinones based on thiol-yne reaction.Covalent assembly of hierarchical particles by efficient coupling of β-diketones and benzyl chlorideWater-Soluble and pH-Responsive Polymeric Nanotubes from Cyclic Peptide TemplatesPreparation of stimuli responsive polycaprolactone membranes of controllable porous morphology via combined atom transfer radical polymerization, ring-opening polymerization and thiol–yne click chemistryThermoresponsive behavior of amphiphilic diblock co-oligomers of ethylene glycol and styrene in aqueous solutionHyperbranched polycaprolactone-click-poly(N-vinylcaprolactam) amphiphilic copolymers and their applications as temperature-responsive membranesThe Ugi reaction in polymer chemistry: syntheses, applications and perspectivesRational design of soluble and clickable polymers prepared by conventional free radical polymerization of acetylene-functionalized acrylateReversible Self-Assembly of Backbone-Thermoresponsive Long Chain Hyperbranched Poly(N-Isopropyl Acrylamide)Efficient synthesis of multifunctional polymers via thiol–epoxy “click” chemistryClick chemistry produces hyper-cross-linked polymers with tetrahedral coresDouble modular modification of thiolactone-containing polymers: towards polythiols and derived structuresHyperbranched Polymers with High Transparency and Inherent High Refractive Index for Application in Organic Light-Emitting DiodesRevisiting thiol-yne chemistry: Selective and efficient monoaddition for block and graft copolymer formationThiyl Glycosylation of Propargylated Octasilsesquioxane: Synthesis and Lectin-Binding Properties of Densely Glycosylated Clusters on a Cubic Platform
P2860
Q34638305-BE1AFEAE-5C20-4EAC-BAD0-01E377938318Q35276655-491173E5-CA42-472A-B1F2-943E29E67461Q36119844-9B2DA0F0-A59C-4BFA-B52D-710FB757E8CCQ37219976-7CA796B7-45F0-48D6-968F-E435BE0C1636Q37653197-643C4EBD-7414-49DF-A7D2-057BEA819572Q37867590-60A0EC72-66E6-4271-86AE-C99C162ADAEDQ37897142-3B414D7A-9F43-43DD-A741-15B68EB171DEQ38059804-47AF5C17-760B-43FC-81FC-5F052BCD9737Q38102638-F198B614-F473-4D98-9997-D24EA6D436F1Q38435973-5FABC7D7-D5A8-4534-893C-1984144C61B6Q39249820-D5483060-3BF3-4569-9D1F-A2C5F7BC540DQ41029036-1B63E16D-D72A-4CE4-882F-23C084447296Q42140841-BD196EFA-B3B6-461F-BA29-943E20F35AE3Q44088252-29D5C710-17DC-4FD8-B037-389B86E95741Q44759074-622B3148-2E52-4D91-9C79-ACEEBE206234Q46073448-442D8F15-F3D6-40C5-ACEC-1A9F02B6CC92Q46475593-1D69D45B-4FF6-49D9-914A-D1BD8881361CQ46850392-5F6ECEB0-04A9-4A34-B885-7CC9B02D2C8AQ47296415-B136F282-A301-423D-ACE1-5695402AD43AQ50093383-ABBDC613-42AF-4E41-90EB-C0EE487E74D0Q50261775-4B7D9919-A8E7-4A07-9031-F078DE6C0BB6Q51097875-281AFAAE-D073-4DC3-B555-7804265EF336Q51672890-46DED302-477B-41A0-A30D-E66701C8F37FQ53541513-23821654-2305-4CAF-AB77-F293169C0AFBQ53637719-730B5D07-AB70-4044-A06F-B92FD6773AEBQ54367731-139226CE-9068-49AA-A8D0-CFDF2B8672F2Q57184759-DA4F0A33-B6D2-4987-B148-9E81F1BFE38AQ57342666-E6DFF737-7A97-4B22-8211-7B958C89F488Q57364228-DA7B3BB3-1C76-4A68-983F-73E282E37199Q57367913-7DBCD1B9-E84C-477B-97AC-6E3B60A48080Q57367956-8DD51DCF-A591-45EA-88EB-36461A19858EQ57368659-DC7D8118-445D-4249-93B5-98262B55F943Q57369154-A7EACD38-A727-4458-BBFD-C9C8EB0F0B58Q57372256-6F2A8F45-F2CF-466C-AE9A-011BD16A929FQ57517629-682A80E5-291D-4394-86BF-C57083B718D7Q57528397-1159C051-2F61-4517-A695-7D79F27381D0Q57711232-1A0EC5EE-41A5-47DF-9A30-865F31831623Q57776898-156B642B-B9F5-4A02-AC78-968C87230308Q57777040-DC06D0EC-F309-448D-94CE-0A5392844AB2Q58381486-8B71198B-55AD-42F5-B8DB-789BF7B8125E
P2860
Hyperbranched polymers by thiol-yne chemistry: from small molecules to functional polymers.
description
2009 nî lūn-bûn
@nan
2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Hyperbranched polymers by thio ...... ecules to functional polymers.
@ast
Hyperbranched polymers by thio ...... ecules to functional polymers.
@en
type
label
Hyperbranched polymers by thio ...... ecules to functional polymers.
@ast
Hyperbranched polymers by thio ...... ecules to functional polymers.
@en
prefLabel
Hyperbranched polymers by thio ...... ecules to functional polymers.
@ast
Hyperbranched polymers by thio ...... ecules to functional polymers.
@en
P356
P1476
Hyperbranched polymers by thio ...... lecules to functional polymers
@en
P2093
Dominik Konkolewicz
P304
18075-18077
P356
10.1021/JA908206A
P407
P577
2009-12-01T00:00:00Z