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.
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Univ Penn, Dept Mat Sci & Engn, Philadelphia, PA 19104 USAUniv Penn, Dept Mat Sci & Engn, Philadelphia, PA 19104 USA
Kim, Ye Chan
Hoang, Son
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Univ Penn, Dept Mat Sci & Engn, Philadelphia, PA 19104 USAUniv Penn, Dept Mat Sci & Engn, Philadelphia, PA 19104 USA
Hoang, Son
Winey, Karen I.
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Univ Penn, Dept Mat Sci & Engn, Philadelphia, PA 19104 USA
Univ Penn, Dept Chem & Biomol Engn, Philadelphia, PA 19104 USAUniv Penn, Dept Mat Sci & Engn, Philadelphia, PA 19104 USA
Winey, Karen I.
Composto, Russell J.
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Univ Penn, Dept Mat Sci & Engn, Philadelphia, PA 19104 USAUniv Penn, Dept Mat Sci & Engn, Philadelphia, PA 19104 USA
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Chulalongkorn Univ, Fac Sci, Program Petrochem & Polymer Sci, Bangkok 10330, Thailand
Chulalongkorn Univ, Ctr Excellence Petrochem & Mat Technol, Bangkok 10330, ThailandChulalongkorn Univ, Fac Sci, Program Petrochem & Polymer Sci, Bangkok 10330, Thailand
Kusolkamabot, Keerati
Sae-ung, Pornpen
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Chulalongkorn Univ, Fac Sci, Program Macromol Sci, Bangkok 10330, ThailandChulalongkorn Univ, Fac Sci, Program Petrochem & Polymer Sci, Bangkok 10330, Thailand
Sae-ung, Pornpen
Niamnont, Nakorn
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King Mongkuts Univ Technol Thonburi, Fac Sci, Dept Chem, Bangkok 10140, ThailandChulalongkorn Univ, Fac Sci, Program Petrochem & Polymer Sci, Bangkok 10330, Thailand
Niamnont, Nakorn
Wongravee, Kanet
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Chulalongkorn Univ, Fac Sci, Dept Chem, Sensor Res Unit, Bangkok 10330, ThailandChulalongkorn Univ, Fac Sci, Program Petrochem & Polymer Sci, Bangkok 10330, Thailand
Wongravee, Kanet
Sukwattanasinitt, Mongkol
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Chulalongkorn Univ, Fac Sci, Dept Chem, Organ Synth Res Unit, Bangkok 10330, ThailandChulalongkorn Univ, Fac Sci, Program Petrochem & Polymer Sci, Bangkok 10330, Thailand
Sukwattanasinitt, Mongkol
Hoven, Voravee P.
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Chulalongkorn Univ, Fac Sci, Dept Chem, Organ Synth Res Unit, Bangkok 10330, ThailandChulalongkorn Univ, Fac Sci, Program Petrochem & Polymer Sci, Bangkok 10330, Thailand