Synthesis of poly(n-butyl acrylate)-block-poly(acrylic acid) diblock copolymers by ATRP and their micellization in water

被引:165
作者
Colombani, Olivier
Ruppel, Markus
Schubert, Frank
Zettl, Heiko
Pergushov, Dmitry V.
Mueller, Axel H. E. [1 ]
机构
[1] Univ Bayreuth, Bayreuther Zentrum Kolloid & Grenzflachenforsch, D-95440 Bayreuth, Germany
[2] Moscow MV Lomonosov State Univ, Fac Chem, Dept Polymer Sci, Moscow 119992, Russia
关键词
D O I
10.1021/ma0609578
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Amphiphilic diblock copolymers, poly(n-butyl acrylate)-block-poly(acrylic acid) (PnBA-PAA), with narrow molecular weight distribution (PDI <= 1.07) were prepared by atom transfer radical polymerization (ATRP) of n-butyl acrylate and tert-butyl acrylate (tBA), followed by selective acidolysis of the PtBA block. These polymers possess a soft PnBA hydrophobic block with a constant chain length of 90-100 monomer units and pH- and ionic strength-sensitive hydrophilic PAA block with DPPAA = 33-300 AA monomer units. They were expected to form stimuli-responsive micelles. The block copolymers with DPPAA ! 100 are directly soluble in water at pH > 4.7. Pyrene steady-state fluorescence spectroscopy and fluorescence correlation spectroscopy (FCS) studies indicate the existence of a very low critical micelle concentration (cmc similar to 10(-8) mol/L). The number-average hydrodynamic radii of the micelles, as determined by FCS, range from 28 to 55 urn, depending on the PAA block length. FCS data indicate that micellar sizes significantly decrease upon dilution for salt-free systems. This is attributed to a dynamic, but kinetically controlled, behavior of these self-assembled nanostructures. In saline solutions the micellar sizes remain constant above the "apparent" cmc (cmc*), which is attributed to slower dynamics of unimer exchange between micelles.
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页码:4338 / 4350
页数:13
相关论文
共 66 条
[1]   Nano-engineering block copolymer aggregates for drug delivery [J].
Allen, C ;
Maysinger, D ;
Eisenberg, A .
COLLOIDS AND SURFACES B-BIOINTERFACES, 1999, 16 (1-4) :3-27
[2]   DIMERIZATION AND TRIMERIZATION OF RHODAMINE 6G IN AQUEOUS-SOLUTION - EFFECT ON THE FLUORESCENCE QUANTUM YIELD [J].
ARBELOA, FL ;
OJEDA, PR ;
ARBELOA, IL .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS II, 1988, 84 :1903-1912
[3]  
Arbeloa FL, 1998, LANGMUIR, V14, P4566
[4]   MICELLIZATION IN BLOCK POLYELECTROLYTE SOLUTIONS .2. FLUORESCENCE STUDY OF THE CRITICAL MICELLE CONCENTRATION AS A FUNCTION OF SOLUBLE BLOCK LENGTH AND SALT CONCENTRATION [J].
ASTAFIEVA, I ;
KHOUGAZ, K ;
EISENBERG, A .
MACROMOLECULES, 1995, 28 (21) :7127-7134
[5]   CRITICAL MICELLIZATION PHENOMENA IN BLOCK POLYELECTROLYTE SOLUTIONS [J].
ASTAFIEVA, I ;
ZHONG, XF ;
EISENBERG, A .
MACROMOLECULES, 1993, 26 (26) :7339-7352
[6]   Self-assembled nanostructures from peptide-synthetic hybrid block copolymers: Complex, stimuli-responsive rod-coil architectures [J].
Babin, J ;
Rodriguez-Hernandez, J ;
Lecommandoux, S ;
Klok, HA ;
Achard, MF .
FARADAY DISCUSSIONS, 2005, 128 :179-192
[7]   RAFTing down under: Tales of missing radicals, fancy architectures, and mysterious holes [J].
Barner-Kowollik, C ;
Davis, TP ;
Heuts, JPA ;
Stenzel, MH ;
Vana, P ;
Whittaker, M .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2003, 41 (03) :365-375
[8]  
Bednarek M, 2000, MACROMOL CHEM PHYSIC, V201, P58, DOI 10.1002/(SICI)1521-3935(20000101)201:1<58::AID-MACP58>3.0.CO
[9]  
2-G
[10]   Pearling instabilities in water-dispersed copolymer cylinders with charged brushes [J].
Bendejacq, D ;
Joanicot, M ;
Ponsinet, V .
EUROPEAN PHYSICAL JOURNAL E, 2005, 17 (01) :83-92