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polymer science (117) 117
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1. Full Text Orthogonal multiple click reactions in synthetic polymer chemistry
by Tunca, Umit
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 11/2014, Volume 52, Issue 22, pp. 3147 - 3165
ABSTRACT This review highlights the concept of multiple click reaction strategy which is utilized for design and synthesis of well‐defined complex... 
post‐functionalization of polymer | copper catalyzed azide‐alkyne cycloaddition (CuAAC) | nitroxide radical coupling (NRC) | Michael thiol‐ene | nucleophilic substitution | thiol‐ene | living polymerization | polymer‐polymer conjugation | thiol‐yne | strain promoted azide‐alkyne cycloaddition (SPAAC) | Diels‐Alder | orthogonal multifunctionalization | Copper Catalyzed azide-alkyne cycloaddition (CuAAC) | Living polymerization | Orthogonal multifunctionalization | Strain promoted azide-alkyne cycloaddition (SPAAC) | Post-functionalization of polymer | Michael thiol-ene | Nitroxide Radical Coupling (NRC) | Diels-Alder | Thiol-yne | Nucleophilic substitution | Polymer-polymer conjugation | Thiol-ene | post-functionalization of polymer | copper catalyzed azide-alkyne cycloaddition (CuAAC) | polymer-polymer conjugation | strain promoted azide-alkyne cycloaddition (SPAAC) | thiol-yne | thiol-ene | POST-FUNCTIONALIZATION | AZIDE-ALKYNE CYCLOADDITION | POLYMER SCIENCE | BLOCK-COPOLYMERS | ONE-POT SYNTHESIS | TRIBLOCK COPOLYMERS | 3-MIKTOARM STAR TERPOLYMERS | THIOL-ENE CLICK | SEQUENTIAL MICHAEL ADDITION | DIELS-ALDER REACTION | HETEROGRAFT COPOLYMERS | Polymerization | Thiols | Polymer industry | Polymers | Polymer chemistry | Strategy | Synthesis | Dealing
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2. Full Text Triple Click Reaction Strategy for Macromolecular Diversity
by Tunca, Umit
Macromolecular Rapid Communications, ISSN 1022-1336, 01/2013, Volume 34, Issue 1, pp. 38 - 46
This Feature Article focuses on the rapidly emerging concept of the “triple click reactions” towards the design and synthesis of macromolecules with... 
nitroxide radical coupling (NRC) | Diels–Alder cycloaddition | copper catalyzed azide–alkyne cycloaddition (CuAAC) | thiol‐ene | living polymerization | copper catalyzed azide-alkyne cycloaddition (CuAAC) | Diels-Alder cycloaddition | thiol-ene | AZIDE-ALKYNE CYCLOADDITION | RADICAL COUPLING REACTIONS | POLYMER SCIENCE | BLOCK-COPOLYMERS | ONE-POT SYNTHESIS | TRIBLOCK COPOLYMERS | 3-MIKTOARM STAR TERPOLYMERS | AMBIENT-TEMPERATURE | TERMINAL ALKYNES | POLYMER CONJUGATION | Copper - chemistry | Ultraviolet Rays | Polymers - chemical synthesis | Click Chemistry | Nitrogen Oxides - chemistry | Polymers - chemistry | Sulfhydryl Compounds - chemistry | Alkynes - chemistry | Azides - chemistry | Cycloaddition Reaction | Polymerization | Copper | Polymers | Molecular weight | Synthesis | Utilization | Molecular weight distribution | Strategy | Resultants | Conjugation
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3. Full Text Contents: Macromol. Chem. Phys. 18/2017
by Tunca, Umit
Macromolecular Chemistry and Physics, ISSN 1022-1352, 09/2017, Volume 218, Issue 18
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4. Full Text Click and Multicomponent Reactions Work Together for Polymer Chemistry
by Tunca, Umit
Macromolecular Chemistry and Physics, ISSN 1022-1352, 08/2018, Volume 219, Issue 16, pp. 1800163 - n/a
This article investigates the current combinations of click and multicomponent reactions (MCRs) to produce complex macromolecular structures through... 
multicomponent reactions | Diels–Alder reactions | click reactions | copper‐catalyzed azide–alkyne cycloaddition reactions | Ugi reactions | Biginelli reactions | thiol‐ene reactions | Passerini reactions | copper-catalyzed azide–alkyne cycloaddition reactions | thiol-ene reactions | copper-catalyzed azide-alkyne cycloaddition reactions | POLYMER SCIENCE | BLOCK-COPOLYMERS | ONE-POT SYNTHESIS | SIDE-CHAIN | UGI 4-COMPONENT REACTION | PASSERINI 3-COMPONENT REACTION | Diels-Alder reactions | FUNCTIONAL POLYMERS | CYCLOADDITION | SEQUENCE | MODULAR SYNTHESIS | POLYAMIDES | Polymers | Polymer industry | Substitution reactions | Organic chemistry | Polymer chemistry | Conjugation | Molecular structure
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5. Full Text Professor Yusuf Yagci at the Age of 65: Still Far Away from Retirement
by Tunca, Umit
Macromolecular Chemistry and Physics, ISSN 1022-1352, 09/2017, Volume 218, Issue 18, pp. 1700352 - n/a
POLYMER SCIENCE | Retirement
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6. Full Text Synthesis of Terpolymers by Click Reactions
by Altintas, Ozcan and Tunca, Umit
Chemistry – An Asian Journal, ISSN 1861-4728, 10/2011, Volume 6, Issue 10, pp. 2584 - 2591
Well‐defined polymeric structures were easily generated through living polymerization systems, in particular, living radical polymerizations. The polymeric... 
catalysis | copper | cycloaddition | radicals | terpolymers | AZIDE-ALKYNE CYCLOADDITION | BLOCK-COPOLYMERS | ONE-POT SYNTHESIS | MIKTOARM STAR TERPOLYMERS | CHEMISTRY, MULTIDISCIPLINARY | THERMO-RESPONSIBILITY | DIELS-ALDER REACTION | TRIBLOCK TERPOLYMERS | RING-OPENING POLYMERIZATION | RADICAL POLYMERIZATION | H-SHAPED TERPOLYMERS | Copper - chemistry | Cyclization | Polymers - chemical synthesis | Click Chemistry | Polymers - chemistry | Alkynes - chemistry | Molecular Structure | Catalysis | Azides - chemistry
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7. Full Text An emerging post‐polymerization modification technique: The promise of thiol‐para‐fluoro click reaction
by Agar, Soykan and Baysak, Elif and Hizal, Gurkan and Tunca, Umit and Durmaz, Hakan
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 06/2018, Volume 56, Issue 12, pp. 1181 - 1198
ABSTRACT Post‐polymerization modification (PPM) of polymers is extremely beneficial in terms of designing brand new synthetic pathways toward functional... 
fluorinated polymers | post‐polymerization modifications | click reactions | pentafluorophenyl | thiol‐para‐fluoro nucleophilic aromatic substitution reactions | thiol-para-fluoro nucleophilic aromatic substitution reactions | post-polymerization modifications | POLYMER SCIENCE | GRAFT-COPOLYMERS | BLOCK-COPOLYMERS | EFFICIENT SYNTHESIS | TRANSFER RADICAL POLYMERIZATION | ENE CLICK | MICHAEL ADDITION | HYPERBRANCHED FLUOROPOLYMERS | CONTAINING POLYMERS | DIELS-ALDER REACTION | CHEMISTRY | Substitution reactions | Polymerization | Thiols | Methods | Organic chemistry | Fluorine | Chemical reactions | Polymers | Fluorination
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8. Full Text Linear tetrablock quaterpolymers via triple click reactions, azide‐alkyne, diels–alder, and nitroxide radical coupling in a one‐pot fashion
by Durmaz, Hakan and Hizal, Gurkan and Tunca, Umit
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 05/2011, Volume 49, Issue 9, pp. 1962 - 1968
Azide‐alkyne and Diels–Alder click reactions together with a click‐like nitroxide radical coupling reaction were used in a one‐pot fashion to generate... 
Diels–Alder cycloaddition reaction | nitroxide radical coupling reaction | poly(tert‐butyl acrylate) | click reactions | quaterpolymer | polystyrene | atom transfer radical polymerization (ATRP) | poly(ε‐caprolactone) | block copolymer | azide‐alkyne cycloaddition reaction | NMR | poly(n‐butyl acrylate) | poly(ethylene glycol) | GPC | ring opening polymerization (ROP) | azide-alkyne cycloaddition reaction | poly(tert-butyl acrylate) | Diels-Alder cycloaddition reaction | poly(Îμ-caprolactone) | poly(n-butyl acrylate) | TRIBLOCK COPOLYMERS | POLYMERIZATION | FUNCTIONALIZED POLYMERS | CHEMISTRY | poly(epsilon-caprolactone) | POLYMER SCIENCE | GRAFT-COPOLYMERS | SET-LRP | MATERIALS SCIENCE | DEFINED BLOCK-COPOLYMERS | MODULAR SYNTHESIS | STAR POLYMERS | Chemical industry | Polystyrene resins | Anthracene | Nuclear magnetic resonance--NMR | Dimethyl formamide | Polyethylene glycol | Liquid chromatography | Coupling | Alkynes | Acrylics | Acrylates | Reproduction | Precursors | Joining | Radicals | Gel permeation chromatography
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9. Full Text Preparation of linear and hyperbranched fluorinated poly(aryl ether‐thioether) through para‐fluoro‐thiol click reaction
by Baysak, Elif and Tunca, Umit and Hizal, Gurkan and Durmaz, Hakan
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 08/2018, Volume 56, Issue 16, pp. 1853 - 1859
ABSTRACT The para‐fluoro‐thiol “click” reaction (PFTCR) was utilized to prepare linear and hyperbranched fluorinated poly (aryl ether‐thioether). For this... 
linear polymers | fluorinated poly(aryl ether‐thioether) | para‐fluoro‐thiol “click” reaction | hyperbranched polymers | fluorinated poly(aryl ether-thioether) | para-fluoro-thiol “click” reaction | POST-FUNCTIONALIZATION | POLYMERS | POLYMER SCIENCE | CHEMISTRY | LIGATION | COPOLYMERS | POWERFUL | para-fluoro-thiol "click" reaction | hyper-branched polymers | TOOL | Polymers | Analysis | Thiols | Infrared spectroscopy | Fourier transforms | Addition polymerization | Nuclear magnetic resonance--NMR | Fluorine | Aromatic compounds | Chemical reactions | Liquid chromatography | Fluorination | Ethane
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10. Full Text Double click reaction strategies for polymer conjugation and post-functionalization of polymers
by Durmaz, Hakan and Sanyal, Amitav and Hizal, Gurkan and Tunca, Umit
Polym. Chem, ISSN 1759-9954, 2012, Volume 3, Issue 4, pp. 825 - 835
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11. Full Text Double click reaction strategies for polymer conjugation and post-functionalization of polymers
by Durmaz, Hakan and Sanyal, Amitav and Hizal, Gurkan and Tunca, Umit
Polymer Chemistry, ISSN 1759-9954, 3/2012, Volume 3, Issue 4, pp. 825 - 835
Double click reaction strategies, which are a combination of different type of click reactions, allow the preparation of polymers with various topologies and... 
POLYMER SCIENCE | FACILE SYNTHESIS | LIVING RADICAL POLYMERIZATION | ONE-POT SYNTHESIS | FRAGMENTATION CHAIN TRANSFER | TRIBLOCK COPOLYMERS | DIELS-ALDER REACTION | HETEROGRAFT COPOLYMERS | MACROMOLECULAR ARCHITECTURES | STAR-BLOCK-COPOLYMERS | THIOL-ENE CLICK
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12. Full Text Synthesis of Activated Ester Functional Polyesters through Light‐Induced [4+4] Cycloaddition Polymerization
by Baysak, Elif and Durmaz, Hakan and Tunca, Umit and Hizal, Gurkan
Macromolecular Chemistry and Physics, ISSN 1022-1352, 09/2017, Volume 218, Issue 18, pp. 1600572 - n/a
A combination of light‐induced [4+4] cycloaddition polymerization and activated ester substitution reaction is demonstrated as a new method to obtain novel... 
perfluorophenyl ester | light‐induced [4+4] cycloaddition polymerization | anthracene dimerization | activated ester substitution | postpolymerization functionalization | light-induced [4+4] cycloaddition polymerization | POST-FUNCTIONALIZATION | POLYMERS | POLYMER SCIENCE | LIGATION | ANTHRACENE | COPOLYMERS | METHACRYLATE | PHOTODIMERIZATION | PENTAFLUOROPHENYL ESTER | CLICK REACTION STRATEGY | CHEMISTRY | Polymerization | Polyols | Infrared spectroscopy | Fourier transforms | Cycloaddition | Anthracene | Nuclear magnetic resonance--NMR | Liquid chromatography | Heat measurement | Polyester resins | Chemical synthesis | Esterification
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13. Full Text Discrete macromolecular constructs via the Diels-Alder "click" reaction
by Hizal, Gurkan and Tunca, Umit and Sanyal, Amitav
Journal of Polymer Science, Part A: Polymer Chemistry, ISSN 0887-624X, 10/2011, Volume 49, Issue 19, pp. 4103 - 4120
Functional polymeric materials with desired properties can be designed by precise control of macromolecular architectures. Over the recent years, click... 
star polymers | click chemistry | Diels-Alder polymers | dendrimers | diblock copolymers | DESIGN | POLYMER SCIENCE | MULTIARM STAR POLYMERS | BLOCK-COPOLYMERS | CYCLOADDITION | CONJUGATION | CHEMISTRY | RADICAL POLYMERIZATION | POLYPHENYLENE DENDRIMERS | MENDABLE POLYMERS | EFFICIENT
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14. Full Text A route toward multifunctional polyurethanes using triple click reactions
by Demirel, Erhan and Durmaz, Hakan and Hizal, Gurkan and Tunca, Umit
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 02/2016, Volume 54, Issue 4, pp. 480 - 486
ABSTRACT The aliphatic polyurethane with pendant alkyne, perfluorophenyl, and anthracene moieties (PU‐anthracene) was prepared from polycondensation of... 
aliphatic polyurethane (PU) | perfluorophenyl ester | differential scanning calorimetry (DSC) | active ester substitution | anthracene | polycondensation | NMR | maleimide | alkyl amine | CuAAC | alkyne | Diels–Alder reaction | azide | Diels-Alder reaction | POLYMERS | POLYMER SCIENCE | OILS | ONE-POT | POLYMERIZATION | FUNCTIONALIZATION | CONJUGATION | CHEMISTRY | Polyurethanes | Furans | Diels-Alder reactions | Polyurethane resins | Cycloaddition | Anthracene | Esters | Aliphatic compounds | Standards | Alkynes
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