Enthalpy-driven micellization of oligocarbonate-fluorene end-functionalized Poly(ethylene glycol)

POLYMER

卷:134

Article

Wei, Guangmin¹  Venkataraman, Shrinivas²  Yang, Yi Yan²  Hedrick, James L.³  Prabhu, Vivek M.¹ 

[1] NIST, Mat Measurement Lab, 100 Bur Dr, Gaithersburg, MD 20899 USA

[2] Nanos, Inst Bioengn & Nanotechnol, 31 Biopolis Way, Singapore 138669, Singapore

[3] IBM Almaden Res Ctr, 650 Harry Rd, San Jose, CA 95120 USA

关键词: Fluorescent probe analysis;    Critical micelle concentration;    Thermodynamics;    ABA triblock copolymer;   

DOI  :  10.1016/j.polymer.2017.11.057

来源: Elsevier

【 摘 要 】

A fluorescent pyrene probe method was applied to measure the critical micelle concentration (CMC) of oligocarbonate-fluorene end-functionalized poly(ethylene glycol) (FmE445Fm) triblock copolymers in water. The CMC decreases with lower temperature and higher values of the hydrophobic block length, m. When analyzed by a closed-assembly micelle model, the estimated energetic parameters find a negative Delta H degrees(mic) and small positive Delta S degrees(mic) suggestive of enthalpy-driven micellization, which differs from entropydriven oxyethylene/oxybutylene triblock copolymers and octaethylene glycol-n-alkyl ethers. The enthalpy-driven micellization of FmE445Fm may result from the limited hydration of individual hydrophobic F blocks that leads to few hydrogen-bonded waters released during F block association. The pi-pi stacking oligocarbonate-fluorene system also observed enthalpy-entropy compensation when compared to a series of published data on diblock and triblock copolymer systems. An anomalously low partition equilibrium constant for m = 15.3 implies a tightly-packed core that excludes pyrene intercalation into the fluorene core. This is discussed along with the possible limited applicability to estimate the CMC and potential model drug molecule insertions into the intercalated micelle core. Published by Elsevier Ltd.

【 授权许可】

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