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Diblock copolymers with amorphous atactic polyferrocenylsilane blocks:: Synthesis, characterization, and self-assembly of polystyrene-block-poly(ferrocenylethylmethylsilane) in the bulk state

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MACROMOLECULES
卷 38, 期 16, 页码 6931-6938

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AMER CHEMICAL SOC
DOI: 10.1021/ma047410i

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Living anionic ring-opening (ROP) polymerization of ethylmethylsila[1]ferrocenophane yields atactic poly(ferrocenylethylmethylsilane) (PFEMS) homopolymers with controlled molecular weights (M. = 4000-41400) and narrow molecular weight distributions (PDI = 1.01-1.02). A series of well-defined polystyrene-block-poly(ferrocenylethylmethylsilane) (PS-b-PFEMS) diblock copolymers was synthesized from styrene and ethylmethylsila[1]ferrocenophane via sequential anionic polymerization. The iron content was readily varied (PFEMS volume fraction = 0.07-0.68), affording high molecular weight (M. = 38 700149 000) iron-rich diblock copolymers with narrow molecular weight distributions (PDI = 1,00-1.07). Both the PFEMS homopolymers and the PS-b-PFEMS diblock copolymers were shown to be amorphous due to the atactic nature of the organometallic block. As a result, PS-b-PFEMS block copolymers readily undergo solid-state self-assembly in the bulk. A spectrum of nanometer-sized iron-rich morphologies has been accessed, and in many cases these arrays were found to be well-ordered over large areas.

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