Photo-living radical polymerization of methyl methacrylate by 2,2,6,6-tetramethylpiperidine-1-oxyl in the presence of a photo-acid generator

被引:43
作者
Yoshida, Eri [1 ]
机构
[1] Toyohashi Univ Technol, Dept Mat Sci, Aichi 4418580, Japan
关键词
Photo-living radical polymerization; 4-Methoxy-2,2,6,6-tetramethylpiperidine-1-oxyl; 2,2 '-Azobis(4-methoxy-2,4-dimethylvaleronitrile); Bis(alkylphenyl)iodonium hexafluorophosphate; Methyl methacrylate; Irradiation; Photo-switching ability; VINYL POLYMERIZATION; PHOTOSENSITIZED INITIATION; ORGANIC POLYSULFIDES; MOLECULAR-WEIGHT; INIFERTER; 4-HYDROXY-2,2,6,6-TETRAMETHYLPIPERIDINE-1-OXYL; PHOTOPOLYMERIZATION; TRANSFORMATION; COPOLYMERS; CARBONYL;
D O I
10.1007/s00396-009-2023-2
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The novel photo-living radical polymerization of methyl methacrylate (MMA) was determined using 2,2'-azobis(4-methoxy-2,4-dimethylvaleronitrile) (AMDV) and 4-methoxy-2,2,6,6-tetramethylpiperidine-1-oxyl (MTEMPO) in the presence of bis(alkylphenyl)iodonium hexafluorophosphate (BAI). The polymerization provided a comparatively narrow molecular weight distribution in the range of 1.4-1.7. The resulting PMMA contained no BAI fragments in its structure and had the 1-cyano-1,3-dimethyl-3-methoxybutyl radical and MTEMPO at the 1:1 molar ratio. The experimental molecular weight was in close agreement with the theoretical one when the initiator efficiency was taken into consideration. The plots of ln([MMA](0)/[MMA]) vs. time and the molecular weight of PMMA vs. the conversion and vs. the reciprocal of the initial concentration of AMDV showed linear correlations, indicating that the polymerization proceeded in accordance with a living mechanism. It was found that the polymerization had a photo-switching ability, because the polymerization was interrupted by turning off the irradiation, and then restarted by the irradiation again.
引用
收藏
页码:767 / 772
页数:6
相关论文
共 48 条
[31]   PHOTOINITIATION OF CATIONIC POLYMERIZATION .3. PHOTOSENSITIZATION OF DIPHENYLIODONIUM AND TRIPHENYLSULFONIUM SALTS [J].
PAPPAS, SP ;
GATECHAIR, LR ;
JILEK, JH .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 1984, 22 (01) :77-84
[32]  
PAPPAS SP, 1989, COMPREHENSIVE POLYM, V4, P337
[34]   GRAFT AND BLOCK PHOTOPOLYMERIZATION [J].
SMETS, G ;
DEWINTER, W ;
DELZENNE, G .
JOURNAL OF POLYMER SCIENCE, 1961, 55 (162) :767-&
[35]   The kinetics of the polymerization of vinyl acetate [J].
Starkweather, HW ;
Taylor, GB .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1930, 52 :4708-4714
[36]   Photoinitiated free radical polymerization using benzoxazines as hydrogen donors [J].
Tasdelen, M. Atilla ;
Kiskan, Baris ;
Yagci, Yusuf .
MACROMOLECULAR RAPID COMMUNICATIONS, 2006, 27 (18) :1539-1544
[37]   DENTAL RESINS WITH REDUCED SHRINKAGE DURING HARDENING [J].
THOMPSON, VP ;
WILLIAMS, EF ;
BAILEY, WJ .
JOURNAL OF DENTAL RESEARCH, 1979, 58 (05) :1522-1532
[38]  
WATANABE H, 1958, KOGYO KAGAKU ZOSSKI, V61, P893
[39]   Synthesis of model A5B1 heteroarm star copolymers using living radical polymerization mediated by 2,2,6,6-tetramethylpiperidine-1-oxyl [J].
Yoshida, E ;
Terazono, T .
POLYMER JOURNAL, 1999, 31 (07) :621-624
[40]   Synthesis of poly(ethylene adipate) with a stable nitroxyl radical at both chain ends, and applications to a counter radical for living radical polymerization [J].
Yoshida, E ;
Nakamura, M .
POLYMER JOURNAL, 1998, 30 (11) :915-920