Solubility and micellization behavior of C60 fullerenes with two well-defined polymer arms

被引:67
作者
Okamura, H [1 ]
Ide, N [1 ]
Minoda, M [1 ]
Komatsu, K [1 ]
Fukuda, T [1 ]
机构
[1] Kyoto Univ, Inst Chem Res, Kyoto 611, Japan
关键词
D O I
10.1021/ma971696s
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
1,4-disubstituted, low-polydispersity C-60 derivatives of the types C-60-(PS)(2), C-60-(PVP)(2), and C-60-(PS-PVP)(2), where PS is polystyrene, PVP is poly(p-vinylphenol), and PS-PVP is a diblock copolymer of this sequence, were prepared by applying the nitroxide-controlled free radical polymerization technique and studied with their solubility behaviors in some organic solvents. The first clear experimental evidence was obtained for the formation of multimolecular micelles of C-60-bearing polymers under certain conditions: for example, Light-scattering measurements showed that the C-60-(PVP)(2), C-60-(PS-PVP)(2), and C-60-(PS)(2) samples with a number-average molecular weight of a polymer arm roughly about 10 000 formed stable micelles in dilute tetrahydrofuran (THF) solution with association numbers of about 20, 6, and 1 (no micellization), respectively. The solvent power of THF for the mother polymers increases in this order. The saturation solubilities S-C60 of the C-60 moiety in C-60-(PS)(2) and C-60-(PVP)(2) were determined. as a function of the PS and PVP chain lengths, showing that, in THF, the S-C60 in the PS adduct is exceptionally large, much larger than that in the PVP adduct of the same chain length, in accord with the mentioned micellization tendency in dilute solution. On the other hand, C-60-(PVP)(2) showed a reasonable solubility in a polar solvent (methanol), in which C-60-(PS)(2) was little soluble. The micellization was found to be accompanied by characteristic changes in the UV-vis spectra, depending on micelle size.
引用
收藏
页码:1859 / 1865
页数:7
相关论文
共 41 条
[1]   The first ''charm bracelet'' conjugated polymer: An electroconducting polythiophene with covalently bound fullerene moieties [J].
Benincori, T ;
Brenna, E ;
Sannicolo, F ;
Trimarco, L ;
Zotti, G ;
Sozzani, P .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1996, 35 (06) :648-651
[2]   THE C-60(2-) FULLERIDE ION [J].
BOYD, PDW ;
BHYRAPPA, P ;
PAUL, P ;
STINCHCOMBE, J ;
BOLSKAR, RD ;
SUN, YP ;
REED, CA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (10) :2907-2914
[3]   FULLERENE-STYRENE RANDOM COPOLYMERS - NOVEL OPTICAL-PROPERTIES [J].
BUNKER, CE ;
LAWSON, GE ;
SUN, YP .
MACROMOLECULES, 1995, 28 (10) :3744-3746
[4]   LIGHT-SCATTERING STUDIES OF COPOLYMERS .1. EFFECT OF HETEROGENEITY OF CHAIN COMPOSITION ON THE MOLECULAR WEIGHT [J].
BUSHUK, W ;
BENOIT, H .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1958, 36 (12) :1616-1626
[5]   FREE-RADICAL POLYMERIZATION OF METHYL-METHACRYLATE AND STYRENE WITH C(60) [J].
CAMP, AG ;
LARY, A ;
FORD, WT .
MACROMOLECULES, 1995, 28 (23) :7959-7961
[6]   FREE-RADICAL COPOLYMERIZATION OF FULLERENES WITH STYRENE [J].
CAO, T ;
WEBBER, SE .
MACROMOLECULES, 1995, 28 (10) :3741-3743
[7]   POLYHYDROXYLATED C-60 CROSS-LINKED POLYURETHANES [J].
CHIANG, LY ;
WANG, LY ;
KUO, CS .
MACROMOLECULES, 1995, 28 (22) :7574-7576
[8]   Covalent fullerene chemistry [J].
Diederich, F ;
Thilgen, C .
SCIENCE, 1996, 271 (5247) :317-323
[9]  
DIEDERICH F, 1992, ANGEW CHEM INT EDIT, V31, P1599
[10]   STRUCTURE AND PHOTOPHYSICS IN C-60-MICELLAR SOLUTIONS [J].
EASTOE, J ;
CROOKS, ER ;
BEEBY, A ;
HEENAN, RK .
CHEMICAL PHYSICS LETTERS, 1995, 245 (06) :571-577