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dc.contributor.authorYağcı, Yusuf
dc.contributor.authorTaskin, Omer Suat
dc.contributor.authorTasdelen, Mehmet Atilla
dc.contributor.authorTemel, Binnur Aydogan
dc.date.accessioned2021-03-05T14:21:02Z
dc.date.available2021-03-05T14:21:02Z
dc.identifier.citationTaskin O. S. , Temel B. A. , Tasdelen M. A. , Yağcı Y., "Synthesis of block copolymers by selective H-abstraction and radical coupling reactions using benzophenone/benzhydrol photoinitiating system", EUROPEAN POLYMER JOURNAL, cilt.62, ss.304-311, 2015
dc.identifier.issn0014-3057
dc.identifier.othervv_1032021
dc.identifier.otherav_b6b277d7-7727-4ef0-ad9e-538dcfc8ec29
dc.identifier.urihttp://hdl.handle.net/20.500.12627/121619
dc.identifier.urihttps://doi.org/10.1016/j.eurpolymj.2014.07.007
dc.description.abstractBlock copolymers were synthesized by a simple photochemical strategy based on selective H-abstraction and radical coupling reactions of ketyl macroradicals. Benzophenone (BP) and benzhydrol (Bzh) end functional polymers were synthesized by atom transfer radical polymerization (ATRP) using functional initiators. Subsequently, the resulting end functional polymers were mixed in 1:1 M ratio and irradiated to form ketyl radicals by hydrogen abstraction of the excited BP moieties from Bzh moieties. The influence of various experimental parameters on the polymerization such as type of polymers and solvents were examined. H-1 NMR, UV and GPC measurements clearly pointed out an efficient photoinduced end coupling reaction between ketyl radicals. (C) 2014 Elsevier Ltd. All rights reserved.
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectPolimer Karakterizasyonu
dc.subjectFizikokimya
dc.subjectTemel Bilimler (SCI)
dc.subjectKimya
dc.subjectPOLİMER BİLİMİ
dc.titleSynthesis of block copolymers by selective H-abstraction and radical coupling reactions using benzophenone/benzhydrol photoinitiating system
dc.typeMakale
dc.relation.journalEUROPEAN POLYMER JOURNAL
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume62
dc.identifier.startpage304
dc.identifier.endpage311
dc.contributor.firstauthorID102977


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