Thermoresponsive Properties of N-Isopropylacrylamide Oligomer Brushes Grafted to Gold Nanoparticles: Effects of Molar Mass and Gold Core Size

被引:73
作者
Shan, Jun [1 ]
Zhao, Yiming [1 ]
Granqvist, Niko [1 ]
Tenhu, Heikki [1 ]
机构
[1] Univ Helsinki, Dept Chem, Polymer Chem Lab, FIN-00014 Hy, Finland
关键词
TRANSFER RADICAL POLYMERIZATION; SELF-ASSEMBLED MONOLAYERS; MOLECULAR-WEIGHT; POLY(N-ISOPROPYLACRYLAMIDE) BRUSHES; THERMAL RESPONSE; UNIMOLECULAR MICELLES; WATER; TEMPERATURE; DENSITY; COLLAPSE;
D O I
10.1021/ma802482e
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
To explore the thermal response of the densely packed inner regime of poly(N-isopropylacrylamide) (PNIPAM) brushes grafted to gold nanoparticles (AuNPs), we systematically studied the thermoresponsive properties of NIPAM oligomeric brushes affected both by oligomer molar mass and Au core size. A series of NIPAM oligomers with various molar masses ranging from ca. 600 to 3400 g/mol were obtained by RAFT polymerization and fractionated with HPLC. The AuNPs stabilized with various NIPAM oligomers were prepared by a one-pot reaction and further fractionated to achieve three pairs of AuNP fractions with narrow size distributions. When decreasing the molar mass of brush chains from ca. 3300 to 700 g/mol, a significant molar mass effect on the thermal transition was found, i.e., the phase transition temperature (defined as the endothermic peak temperature T-p by DSC) shifted from ca. 31 to 15 degrees C and the endothermic peak became broadened. As a comparison, we also studied the aqueous solutions of free NIPAM oligomers (molar mass from ca. 3400 to 600 g/mol) by turbidity measurements. They showed a completely opposite trend of the thermally induced phase transitions; i.e., the transition shifted to higher temperature with decreasing molar mass. The Au core size also affected the thermal response of NIPAM oligomer brushes, especially in the case of the shortest oligomers. Large Au cores caused the thermal transition of NIPAM oligomer brush to occur at lower temperatures compared to the small Au cores. This was attributed to the hydrophobic nature of Au nanocrystal surfaces. Enthalpy changes (Delta H) associated with the thermal transitions of the oligomer brushes are indicative of strong interchain interactions in the brushes, especially on large Au cores.
引用
收藏
页码:2696 / 2701
页数:6
相关论文
共 33 条
[1]  
Advincula R. C., 2004, POLYM BRUSHES SYNTHE
[2]   Temperature dependence of the colloidal stability of neutral amphiphilic polymers in water [J].
Aseyev, VO ;
Tenhu, H ;
Winnik, FM .
CONFORMATION-DEPENDENT DESIGN OF SEQUENCES IN COPOLYMERS II, 2006, 196 (1-85) :1-85
[3]   Thermal response of poly(N-isopropylacrylamide) brushes probed by surface plasmon resonance [J].
Balamurugan, S ;
Mendez, S ;
Balamurugan, SS ;
O'Brien, MJ ;
López, GP .
LANGMUIR, 2003, 19 (07) :2545-2549
[4]  
BORISOV OV, 2008, SMART POLYM APPL BIO
[5]   Surface rearrangement of diblock copolymer brushes - Stimuli responsive films [J].
Brittain, William J. ;
Boyes, Stephen G. ;
Granville, Anthony M. ;
Baum, Marina ;
Mirous, Brian K. ;
Akgun, Bulent ;
Zhao, Bin ;
Blickle, Carl ;
Foster, Mark D. .
SURFACE- INITIATED POLYMERIZATION II, 2006, 198 (125-147) :125-147
[6]   A structural definition of polymer brushes [J].
Brittain, William J. ;
Minko, Sergiy .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2007, 45 (16) :3505-3512
[7]   Polymer-stabilized gold nanoparticles with high grafting densities [J].
Corbierre, MK ;
Cameron, NS ;
Lennox, RB .
LANGMUIR, 2004, 20 (07) :2867-2873
[8]   Synthesis and thermoresponsive property of end-functionalized poly(N-isopropylacrylamide) with pyrenyl group [J].
Duan, Q ;
Miura, Y ;
Narumi, A ;
Shen, X ;
Sato, S ;
Satoh, T ;
Kakuchi, T .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2006, 44 (03) :1117-1124
[9]   MALDI-TOF MS investigation of the RAFT polymerization of a water-soluble acrylamide derivative [J].
Favier, A ;
Ladavière, C ;
Charreyre, MT ;
Pichot, C .
MACROMOLECULES, 2004, 37 (06) :2026-2034
[10]   Effects of end group polarity and molecular weight on the lower critical solution temperature of poly(N-isopropylacrylamide) [J].
Furyk, S ;
Zhang, YJ ;
Ortiz-Acosta, D ;
Cremer, PS ;
Bergbreiter, DE .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2006, 44 (04) :1492-1501