TY - JOUR
T1 - Polymeric nanosphere formed from temperature-responsive polymer composed of (N,N-dimethylamino)ethyl methacrylate and ethyl acrylamide
AU - Lee, Tae Bum
AU - No, Kyoung Tai
AU - Cho, Sun Hang
AU - Kim, Seung Su
AU - Seo, Jung Ki
AU - Lee, Jin Ho
AU - Yuk, Soon Hong
PY - 2001/3/1
Y1 - 2001/3/1
N2 - A nanosphere was formed from a temperature-responsive random copolymer of (N,N-dimethylamino)ethyl methacrylate (DMAEMA) and ethyl acrylamide (EAAm) without a crosslinker. When the copolymerization was performed in a water/ethanol solvent mixture (90/10 v/v %) above the lower critical-solution temperature of poly(DMAEMA-co-EAAm), the nanosphere was formed with the propagation of copolymerization. Atomic force microscopy analysis and dynamic light scattering both showed the formation of nanosphere and the size was decreased as the EAAm content increased in the copolymer. To illuminate this nanosphere formation phenomena, molecular dynamic simulations were performed with model polymer solutions. According to the analysis of the simulation trajectory, the ethyl groups of ethanol bind to the hydrophobic sites of poly(DMAEMA) or poly(DMAEMA-co-EAAm), and water molecules can bind preferentially to C double bond O groups that are abundant on the surface of the core, which is composed of oligomer and ethanol. This may enable the polymerization to proceed within the core, which is transformed into nanosphere.
AB - A nanosphere was formed from a temperature-responsive random copolymer of (N,N-dimethylamino)ethyl methacrylate (DMAEMA) and ethyl acrylamide (EAAm) without a crosslinker. When the copolymerization was performed in a water/ethanol solvent mixture (90/10 v/v %) above the lower critical-solution temperature of poly(DMAEMA-co-EAAm), the nanosphere was formed with the propagation of copolymerization. Atomic force microscopy analysis and dynamic light scattering both showed the formation of nanosphere and the size was decreased as the EAAm content increased in the copolymer. To illuminate this nanosphere formation phenomena, molecular dynamic simulations were performed with model polymer solutions. According to the analysis of the simulation trajectory, the ethyl groups of ethanol bind to the hydrophobic sites of poly(DMAEMA) or poly(DMAEMA-co-EAAm), and water molecules can bind preferentially to C double bond O groups that are abundant on the surface of the core, which is composed of oligomer and ethanol. This may enable the polymerization to proceed within the core, which is transformed into nanosphere.
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U2 - 10.1002/1099-0488(20010301)39:5<594::AID-POLB1033>3.0.CO;2-J
DO - 10.1002/1099-0488(20010301)39:5<594::AID-POLB1033>3.0.CO;2-J
M3 - Article
AN - SCOPUS:0035282260
SN - 0887-6266
VL - 39
SP - 594
EP - 600
JO - Journal of Polymer Science, Polymer Letters Edition
JF - Journal of Polymer Science, Polymer Letters Edition
IS - 5
ER -