Glycoconjugated polymer.: 5.: Synthesis and characterization of a seven-arm star polystyrene with β-cyclodextrin core based on TEMPO-mediated living radical polymerization

被引:60
作者
Kakuchi, T [1 ]
Narumi, A
Matsuda, T
Miura, Y
Sugimoto, N
Satoh, T
Kaga, H
机构
[1] Hokkaido Univ, Grad Sch Engn, Div Mol Chem, Sapporo, Hokkaido 0608628, Japan
[2] Natl Inst Adv Ind Sci & Technol, AIST, Sapporo, Hokkaido 0628517, Japan
关键词
D O I
10.1021/ma021296r
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
beta-Cyclodextrin (-CyD) was modified into a seven-functional initiator (1) for 2,2,6,6-tetramethylpiperidinyloxy- (TEMPO-) mediated living radical polymerization. Styrene (St) was polymerized with 1 under several conditions to afford original products I-IV. Size exclusion chromatography (SEC) traces of I-IV exhibited trimodal molecular weight distributions; hence, they were fractionated into the respective three species, i.e., main products 2, byproducts 3 with lower molecular weights, and byproducts 4 with higher molecular weights. The weight-average molecular weights determined by SEC and static laser light scattering measurement (M-w,M-SEC and M-w,M-SLS,M- respectively) were 1.34 x 10(4) and ;2.98 x 10(4) for 2-I, 4.52 x 10(4) and 6.77 x 10(4) for 2-II, 1.35 x 10(5) and 1.87 x 10(5) for 2-III, and 9.67 x 10(5) and 1.89 x 10(6) for 2-IV. The M-w,M-SLS's were larger than the respective M-w,M-SEC's. In the H-1 NMR spectra of 2, the signals due to polystyrene (PSt) appeared along with the characteristic signals due to the 1 unit. therefore, those of 2 were assignable to a star PSt with an acetylated beta-CyD core. Polymer 2 was treated with sulfuric acid to give. core-cleaved polymer 2'. The M-w,M-SEC's were 2.80 x 10(3), 9.60 x 10(3), 2.70 x 10(4), and 2.61 x 10(5) for 2'-I, 2-II, 2'-III, and 2'-IV, indicating that the arm number of 2, N-PSt, was seven. The byproducts 3 and 4 were characterized and found to be a TEMPO-terminated linear PSt and a star-star coupled polymer, respectively. The seven-arm star PSt with a beta-CyD core, 5, was obtained through deacetylation of 2 using sodium methoxide in dry THF. The M-w,M-SLS values were 3.96 x 10(5), 3.78 x 10(5), 2.40 x 10(5), and 1.94 x 10(6) for 5-I, 5-II, 5-III, and 5-IV. Hence, 5-I and 5-II showed aggregation in a good solvent for PSt with aggregation-numbers (N-A) of 13 and 6, respectively.
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页码:3914 / 3920
页数:7
相关论文
共 36 条
[1]   Atom transfer radical polymerization of styrene using a novel octafunctional initiator: Synthesis of well-defined polystyrene stars [J].
Angot, S ;
Murthy, KS ;
Taton, D ;
Gnanou, Y .
MACROMOLECULES, 1998, 31 (21) :7218-7225
[2]   Amino acid derivatives of beta-cyclodextrin [J].
Ashton, PR ;
Koniger, R ;
Stoddart, JF ;
Alker, D ;
Harding, VD .
JOURNAL OF ORGANIC CHEMISTRY, 1996, 61 (03) :903-908
[3]   Core-functionalized star polymers by transition metal-catalyzed living radical polymerization. 2. Selective interaction with protic guests via core functionalities [J].
Baek, KY ;
Kamigaito, M ;
Sawamoto, M .
MACROMOLECULES, 2002, 35 (05) :1493-1498
[4]   Core-functionalized star polymers by transition metal-catalyzed living radical polymerization. 1. Synthesis and characterization of star polymers with PMMA arms and amide cores [J].
Baek, KY ;
Kamigaito, M ;
Sawamoto, M .
MACROMOLECULES, 2001, 34 (22) :7629-7635
[5]  
Dao J, 1998, J POLYM SCI POL CHEM, V36, P2161, DOI 10.1002/(SICI)1099-0518(19980915)36:12<2161::AID-POLA24>3.0.CO
[6]  
2-3
[7]  
DAVIS TP, 1995, TRENDS POLYM SCI, V3, P365
[8]   Multifunctional coupling agents for living cationic polymerization .6. Synthesis of multiarmed and end-functionalized poly(alpha-methylstyrene) with multifunctional silyl enol ethers [J].
Fukui, H ;
Deguchi, T ;
Sawamoto, M ;
Higashimura, T .
MACROMOLECULES, 1996, 29 (04) :1131-1137
[9]  
GEORGES MK, 1994, TRENDS POLYM SCI, V2, P66
[10]   Polymers with complex architecture by living anionic polymerization [J].
Hadjichristidis, N ;
Pitsikalis, M ;
Pispas, S ;
Iatrou, H .
CHEMICAL REVIEWS, 2001, 101 (12) :3747-3792