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Focal Point Association of Core-Crystalline Micelles with an Amphiphilic Corona Block

化学 两亲性 胶束 日冕(行星地质学) 块(置换群论) 芯(光纤) 联想(心理学) 共聚物 有机化学 光学 组合数学 天体生物学 聚合物 维纳斯 水溶液 哲学 物理 认识论 数学
作者
Shaofei Song,Junting Xu,Hang Zhou,Ian Manners,Mitchell A. Winnik
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
标识
DOI:10.1021/jacs.5c00926
摘要

We report the preparation of star-like supermicelles by the secondary association of triblock comicelles or scarf-like micelles driven by a change in solvency. These building blocks were synthesized by seeded growth in which crystallites of a triblock terpolymer, either PFS27-b-PTDMA81-b-POEGMA45 (to form triblock comicelles) or PFS66-b-PTDMA81-b-POEGMA45 (to form scarf-like micelles), served as seeds for crystallization-driven self-assembly (CDSA). PFS-b-PTDMA unimers were added in the seeded growth step. The corona-forming block PTDMA-POEGMA is amphiphilic and sensitive to polarity changes of the solvents. We sought solvents in which the upper critical solution temperature (UCST, TUCST) of POEGMA was slightly above room temperature (RT). Examples included 1-decanol and 1-decanol/decane mixtures. Seeded growth proceeded normally in solvents above the UCST of POEGMA. When the solution temperature was lowered below TUCST, or when the triblock comicelles or scarf-like micelles were transferred to a solvent (e.g., 1-decanol) below its TUCST, the center blocks associated to form star-like supermicelles. The addition of small amounts of THF to the medium to increase the solvency for POEGMA led to dissociation of the supermicelles. Transfer of the triblock comicelles to 1-pentanol at RT, below the UCST of PTDMA, also led to controlled secondary association to form supermicelles with a different morphology. Seeded growth with PFS25-b-PDMAEMA184 unimers led to supermicelles in which the poly(dimethylaminoethyl methacrylate) corona chains could serve as carriers for gold nanoparticles (AuNPs). These AuNP@supermicelle complexes could serve as recoverable catalysts, for example to catalyze the condensation polymerization of bis(dimethylsilyl)benzene and pentanediol. They were highly active catalysts and showed excellent mechanical robustness for recovery and reuse.

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