RAFT polymerization of diacrylate derivatives having different spacers in dilute conditions

被引:30
作者
Mori, Hideharu [1 ,2 ]
Tsukamoto, Masahiro [1 ]
机构
[1] Yamagata Univ, Dept Polymer Sci & Engn, Grad Sch Sci & Engn, Yonezawa, Yamagata 9928510, Japan
[2] Yamagata Univ, Dept Organ Device Engn, Grad Sch Sci & Engn, Yonezawa, Yamagata 9928510, Japan
关键词
RAFT polymerization; Divinyl monomer; Branched polymer; FRAGMENTATION CHAIN-TRANSFER; TRANSFER RADICAL POLYMERIZATION; BRANCHED POLY(METHYL METHACRYLATE)S; XANTHATE-MEDIATED POLYMERIZATION; BLOCK-COPOLYMERS; ACRYLIC-ACID; MOLECULAR-WEIGHT; STAR POLYMERS; VINYL-ACETATE; CYCLOPOLYMERIZATION;
D O I
10.1016/j.polymer.2010.12.032
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理];
摘要
Reversible addition-fragmentation chain transfer (RAFT) polymerization of four divinyl monomers, 1,4-butanediol diacrylate (BDDA) and three poly(ethylene glycol) diacrylates (PEGDAs), were investigated under dilute conditions ([M] = 0.2-0.05 mol/L). RAFT polymerization of BDDA using a dithiocarbamate-type chain transfer agent (CIA) afforded soluble polymers, whereas a cross-linked product was obtained by conventional radical polymerization. The monomer concentration, the nature of the CIA, and the CTA/initiator ratio were found to affect the polymerization behavior and structure of the resulting polymers, which is attributed to the relative propensities for intermolecular propagating/cross-linking reactions and intramolecular cyclization. RAFT polymerizations of three PEGDAs (PEG258DA, average M-n = 258; PEG575DA, average M-n = 575; PEG700DA, average M-n = 700) having different lengths of PEG spacers (n = 3, 10, 13, respectively) were also conducted under dilute conditions. Water-soluble polymers were synthesized by one-step RAFT polymerization of PEGDAs having longer spacers (n = 10 and 13), whereas RAFT polymerization of PEGDA (n = 3) afforded polymers soluble in organic solvents. The product obtained by RAFT polymerization of PEGDA (n = 10) showed a characteristic thermoresponsive property, lower critical solution temperature (LCST), in aqueous solution. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:635 / 645
页数:11
相关论文
共 62 条
[1]
Controlled/living ring-closing cyclopolymerization of diallyldimethylammonium chloride via the reversible addition fragmentation chain transfer process [J].
Assem, Yasser ;
Chaffey-Millar, Hugh ;
Barner-Kowollik, Christopher ;
Wegner, Gerhard ;
Agarwal, Seema .
MACROMOLECULES, 2007, 40 (11) :3907-3913
[2]
Development of branching in living radical copolymerization of vinyl and divinyl monomers [J].
Bannister, Iveta ;
Billingham, Norman C. ;
Armes, Steven P. ;
Rannard, Steven P. ;
Findlay, Paul .
MACROMOLECULES, 2006, 39 (22) :7483-7492
[3]
Camp W.V., 2010, J POLYM SCI A, V48, P2016
[4]
Thiocarbonylthio compounds (S=C(Z)S-R) in free radical polymerization with reversible addition-fragmentation chain transfer (RAFT polymerization). Effect of the activating group Z [J].
Chiefari, J ;
Mayadunne, RTA ;
Moad, CL ;
Moad, G ;
Rizzardo, E ;
Postma, A ;
Skidmore, MA ;
Thang, SH .
MACROMOLECULES, 2003, 36 (07) :2273-2283
[5]
PHOTOPOLYMERIZATION KINETICS OF OLIGO(ETHYLENE OXIDE) AND OLIGO(METHYLENE) OXIDE DIMETHACRYLATES [J].
COOK, WD .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 1993, 31 (04) :1053-1067
[6]
Substituent effects in xanthate-mediated polymerization of vinyl acetate: Ab initio evidence for an alternative fragmentation pathway [J].
Coote, ML ;
Radom, L .
MACROMOLECULES, 2004, 37 (02) :590-596
[7]
Macromolecular design via the interchange of xanthates (MADIX): Polymerization of styrene with O-ethyl xanthates as controlling agents [J].
Destarac, M ;
Brochon, C ;
Catala, JM ;
Wilczewska, A ;
Zard, SZ .
MACROMOLECULAR CHEMISTRY AND PHYSICS, 2002, 203 (16) :2281-2289
[8]
Controlled/Living Cyclopolymerization of tert-Butyl α-(Hydroxymethyl) Acrylate Ether Dimer via Reversible Addition Fragmentation Chain Transfer Polymerization [J].
Erkoc, Selda ;
Acar, A. Ersin .
MACROMOLECULES, 2008, 41 (23) :9019-9024
[9]
Experimental requirements for an efficient control of free-radical polymerizations via the reversible addition-fragmentation chain transfer (RAFT) process [J].
Favier, Arnaud ;
Charreyre, Marie-Therese .
MACROMOLECULAR RAPID COMMUNICATIONS, 2006, 27 (09) :653-692
[10]
Block copolymers of acrylic acid and butyl acrylate prepared by reversible addition-fragmentation chain transfer polymerization: Synthesis, characterization, and use in emulsion polymerization [J].
Gaillard, N ;
Guyot, A ;
Claverie, J .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2003, 41 (05) :684-698