Initiator-fragment incorporation radical polymerization of ethylene glycol dimethacrylate in the presence of 1,1-diphenylethylene: synthesis and characterization of soluble hyperbranched polymer nanoparticles

被引:20
作者
Sato, T [1 ]
Miyagi, T [1 ]
Hirano, T [1 ]
Seno, M [1 ]
机构
[1] Univ Tokushima, Fac Engn, Dept Chem Sci & Technol, Tokushima 7708506, Japan
关键词
initiator-fragment incorporation radical polymerization; hyperbranched polymer; electron spin resonance; nanoparticle; divinyl monomer; crosslinker;
D O I
10.1002/pi.1575
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The polymerization of ethylene glycol dimethacrylate (EGDMA) as crosslinker was carried out at 70 and 80 degreesC in benzene using dimethyl 2,2'-azobisisobutyrate (MAIB) as initiator at concentrations as high as 0.50-0.70 mol l(-1) in the presence of 1,1-diphenylethylene (DPE), where the concentrations of EGDMA and DPE were 0.50-0.70 and 0.25-0.50 mol l(-1), respectively. The polymerization proceeded homogeneously, without gelation, to give soluble polymers. The yield and molecular weight of the resulting polymers increased with time. The homogeneous polymerization system involved ESR-observable DPE-derived radicals of considerably high concentration (3.6-5.3 x 10(-5) mol l(-1)). The methoxycarbonylpropyl groups as MAIB-fragments were incorporated as a main constituent (35-50 mol%) into the polymers (initiator-fragment incorporation radical polymerization). The polymers also contained DPE units (15 mol%) and EGDMA units with double bonds (10-25 mol%) and without double bonds (20 mol%). Results from gel permeation chromatography (GPC)-multiangle laser light scattering (MALLS), transmission electron microscopy (TEM) and viscometric measurements revealed that the individual polymer molecules were formed as hyperbranched nanoparticles. (C) 2004 Society of Chemical Industry.
引用
收藏
页码:1503 / 1511
页数:9
相关论文
共 39 条
[1]   From terphenyl-dendronized macromonomers to aromatic-aliphatic polyethers bearing two pendant dendrons per repeating unit [J].
Andreopoulou, AK ;
Kallitsis, JK .
MACROMOLECULES, 2002, 35 (15) :5808-5815
[2]  
BLEDZKI A, 1985, MAKROMOL CHEM-RAPID, V6, P649
[3]   A novel thermal iniferter for radical polymerization [J].
Chen, XP ;
Qiu, KY ;
Swift, G ;
Westmoreland, DG ;
Wu, SQ .
EUROPEAN POLYMER JOURNAL, 2000, 36 (08) :1547-1554
[4]  
GROENENBOOM CJ, 1982, MAKROMOL CHEM, V183, P281
[5]   Control of polymer topology through transition-metal catalysis: Synthesis of hyperbranched polymers by cobalt-mediated free radical polymerization [J].
Guan, Z .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (20) :5616-5617
[6]   1,1-Di(p-tolyl)ethylene:: a versatile radical scavenger [J].
Hageman, HJ .
EUROPEAN POLYMER JOURNAL, 1999, 35 (06) :991-996
[7]   PREPARATION OF HYPERBRANCHED AND STAR POLYMERS BY A LIVING, SELF-CONDENSING FREE-RADICAL POLYMERIZATION [J].
HAWKER, CJ ;
FRECHET, JMJ ;
GRUBBS, RB ;
DAO, J .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (43) :10763-10764
[8]   Hyperbranched polyacrylates prepared by self-condensing vinyl copolymerization in the presence of a tetrafunctional initiator [J].
Hong, CY ;
Zou, YF ;
Pan, CY .
POLYMER INTERNATIONAL, 2003, 52 (02) :257-264
[9]   Preparation and characterization of hyperbranched polyacrylate copolymers by self-condensing vinyl copolymerization (SCVCP) [J].
Hong, CY ;
Pan, CY .
POLYMER INTERNATIONAL, 2002, 51 (09) :785-791
[10]  
Hult A, 1999, ADV POLYM SCI, V143, P1