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Photoinduced Free Radical Promoted Copper(I)-Catalyzed Click Chemistry for Macromolecular Syntheses

dc.contributor.authorTasdelen, Mehmet Atilla
dc.contributor.authorYilmaz, Gorkem
dc.contributor.authorIskin, Birol
dc.contributor.authorYagci, Yusuf
dc.date.accessioned2026-01-26T00:56:29Z
dc.date.issued2011-12-09
dc.description.abstractPhotoinduced copper(I)-catalyzed Huisgen 1,3-dipolar cycloaddition (CuAAC) via photoinduced electron transfer using free radical photoinitiators has been developed as a new platform to serve as orthogonal click system. Photoinitiators acting at near UV and visible range, namely 2, 2-dimethoxy-2-phenyl acetophenone, 2-benzyl-2-dimethylamino-4′-morpholino butyrophenone, 2,4,6-trimethylbenzoyl)diphenylphosphine oxide, dicyclopentadienyl bis[2,6-difluoro-3-(1-pyrrolyl)phenyl] titanium) and camphorquinone/benzyl alcohol were tested with copper(II) chloride/N,N,N′,N″,N″-pentamethyldiethylenetriamine complex to catalyze the CuAAC via photoinduced electron transfer reaction. This strategy has been applied in construction of various macromolecular architectures including telechelic polymers and block copolymers. Spectroscopic and chromatographic investigations revealed that successful macromolecular syntheses have been achieved by this technique.
dc.description.urihttps://doi.org/10.1021/ma202438w
dc.description.urihttps://dx.doi.org/10.1021/ma202438w
dc.identifier.doi10.1021/ma202438w
dc.identifier.eissn1520-5835
dc.identifier.endpage61
dc.identifier.issn0024-9297
dc.identifier.openairedoi_dedup___::b48e75eefa1f41c9106b7cb3744a0410
dc.identifier.orcid0000-0002-8638-4548
dc.identifier.startpage56
dc.identifier.urihttps://hdl.handle.net/11527/55151
dc.identifier.volume45
dc.language.isoeng
dc.publisherAmerican Chemical Society (ACS)
dc.relation.ispartofMacromolecules
dc.sdg.typeGoal 3: Good Health and Well-being
dc.titlePhotoinduced Free Radical Promoted Copper(I)-Catalyzed Click Chemistry for Macromolecular Syntheses
dc.typeArticle
dspace.entity.typePublication

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