A kinetic study of atom transfer radical polymerization of styrene with bis(2-pyridyl)ethylenedimethanimine derivative ligands

被引:3
作者
Arslan, Hulya [1 ]
Kucuk, Yasemin [1 ]
Mentes, Ayfer [2 ]
Acar, Metin Hayri [3 ]
机构
[1] Bulent Ecevit Univ, Dept Chem, Zonguldak, Turkey
[2] Aksaray Univ, Dept Chem, Aksaray, Turkey
[3] Istanbul Tech Univ, Dept Chem, TR-80626 Istanbul, Turkey
关键词
Polymer synthesis; controlled radical polymerization; ATRP; imine ligand; N-BUTYL ACRYLATE; METHYL-METHACRYLATE; BLOCK-COPOLYMERS; HYPERBRANCHED GLYCOPOLYMERS; TRIBLOCK COPOLYMERS; GRAFT-COPOLYMERS; ATRP; CATALYSTS; EFFICIENCY; SYSTEM;
D O I
10.3906/kim-1302-64
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Atom transfer radical polymerization (ATRP) of styrene was carried out with multidentate nitrogen-based ligands, namely N,N'-bis[phenyl(pyrid-2-yl) methylene]ethane-1,2-diamine (BPDA) and N, N'-bis[methyl(pyrid-2-yl) methylene]ethane-1,2-diamine (BMDA), and catalyst systems at catalyst/ligand molar ratios of 1/0.33, 1/0.5, 1/1, and 1/1.5 by using 2 different initiators, (1-bromoethyl) benzene (BEB) and ethyl-2-bromopropionate (EBP). Linear first-order kinetic plots were observed for ATRP of styrene upon using BPDA as a ligand with both initiators. Even though the linear slopes indicate that radical concentration remains constant during reactions, high molecular weights were obtained at low conversion and showed a linear relation thereafter. To investigate the molecular weight effect, reactions were also performed in the presence of (1-bromoethyl) benzene initiator in dimethylformamide (DMF) for BPDA and in toluene for BMDA using a catalyst/ligand ratio of 1/1.
引用
收藏
页码:824 / 831
页数:8
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