Synthesis and characterization of graft copolymers by photoinduced CuAAC click chemistry
Yazarlar (2)
Gülşah Demirci Yalova Üniversitesi
Prof. Dr. Mehmet Atilla TAŞDELEN Yalova Üniversitesi, Türkiye
Makale Türü Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale)
Dergi Adı European Polymer Journal
Dergi ISSN 0014-3057 Wos Dergi Scopus Dergi
Dergi Tarandığı Indeksler SSCI
Makale Dili İngilizce Basım Tarihi 05-2015
Kabul Tarihi Yayınlanma Tarihi 01-05-2015
Cilt / Sayı / Sayfa 66 / 0 / 282–289 DOI 10.1016/j.eurpolymj.2015.02.029
Makale Linki http://linkinghub.elsevier.com/retrieve/pii/S0014305715001044
Özet
Well-defined graft copolymers were synthesized by a simple photoinduced copper(I) catalyzed 1,3-dipolar cycloaddition click reaction of alkyne-terminated poly(epsilon-caprolactone) (PCL) either side-chain azide-functional polystyrene (PSt) or poly(vinyl chloride) (PVC). The alkyne-terminated PCL was prepared by ring-opening polymerization of epsilon-caprolactone in bulk using Sn(Oct)2 as a catalyst and propargyl alcohol as an initiator. Whereas, the halide groups of PVC and poly(styrene-co-chloromethylstyrene) prepared by nitroxide mediated radical copolymerization were transformed to side chain azide-functional PVC or PSt via nucleophilic substitution reaction using sodium azide. Subsequently, the resulting alkyne and azide functional polymers were mixed in DMF with Cu(II)Br-2/PMDETA ligand and 2,2-dimethoxy-2-phenyl acetophenone and irradiated by UV light to form corresponding graft copolymers. The FT-IR, H-1 NMR, GPC and DSC analyzes clearly pointed out an efficient photoinduced CuAAC click reactions between azide- and alkyne-functional precursor polymers. (C) 2015 Elsevier Ltd. All rights reserved.
Anahtar Kelimeler
Copper-catalyzed azide-alkyne cycloaddition | Click chemistry | Graft copolymers | Photoinduced reactions | Ring-opening polymerization
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
Synthesis and characterization of graft copolymers by photoinduced CuAAC click chemistry

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