Giant Molecular Shape Amphiphiles Based on Polystyrene鈥揌ydrophilic [60]Fullerene Conjugates: Click Synthesis, Solution Self-Assembly, and Phase Behavior

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• 作者：Xinfei Yu ; Wen-Bin Zhang ; Kan Yue ; Xiaopeng Li ; Hao Liu ; Yu Xin ; Chien-Lung Wang ; Chrys Wesdemiotis ; Stephen Z. D. Cheng
• 刊名：The Journal of the American Chemical Society
• 出版年：2012
• 出版时间：May 9, 2012
• 年：2012
• 卷：134
• 期：18
• 页码：7780-7787
• 全文大小：431K
• 年卷期：v.134,no.18(May 9, 2012)
• ISSN：1520-5126

文摘

This paper reports a comprehensive study on the synthesis and self-assembly of two model series of molecular shape amphiphiles, namely, hydrophilic [60]fullerene (AC₆₀) tethered with one or two polystyrene (PS) chain(s) at one junction point (PS_n鈥揂C₆₀ and 2PS_n鈥揂C₆₀). The synthesis highlighted the regiospecific multiaddition reaction for C₆₀ surface functionalization and the Huisgen 1,3-dipolar cycloaddition between alkyne functionalized C₆₀ and azide functionalized polymer to give rise to shape amphiphiles with precisely defined surface chemistry and molecular topology. When 1,4-dioxane/DMF mixture was used as the common solvent and water as the selective solvent, these shape amphiphiles exhibited versatile self-assembled micellar morphologies which can be tuned by changing various parameters, such as molecular topology, polymer tail length, and initial molecular concentration, as revealed by transmission electron microscopy and light scattering experiments. In the low molecular concentration range of equal or less than 0.25 (wt) %, micellar morphology of the series of PS_n鈥揂C₆₀ studied was always spheres, while the series of 2PS_n鈥揂C₆₀ formed vesicles. Particularly, PS₄₄鈥揂C₆₀ and 2PS₂₃鈥揂C₆₀ are synthesized as a topological isomer pair of these shape amphiphiles. PS₄₄鈥揂C₆₀ formed spherical micelles while 2PS₂₃鈥揂C₆₀ generated bilayer vesicles under identical conditions. The difference in the self-assembly of PS_n鈥揂C₆₀ and 2PS_n鈥揂C₆₀ was understood by the molecular shape aspect ratio. The stretching ratio of PS tails decreased with increasing PS tail length in the spherical micelles of PS_n鈥揂C₆₀, indicating a micellar behavior that changes from small molecular surfactant-like to amphiphilic block copolymer-like. For the series of PS_n鈥揂C₆₀ in the high molecular concentration range [>0.25 (wt) %], their micellar morphological formation of spheres, cylinders, and vesicles was critically dependent upon both the initial molecular concentration and the PS tail length. On the other hand, the series of 2PS_n鈥揂C₆₀ remained in the state of bilayer vesicles in the same concentration range. Combining both of the experimental results obtained in the low and high molecular concentrations, a systematic morphological phase diagram was constructed for the series of PS_n鈥揂C₆₀ with different PS tail lengths. The versatile and concentration-sensitive phase behaviors of these molecular shape amphiphiles are unique and have not been systematically explored in the traditional surfactants and block copolymers systems.