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Updated: Apr 27, 2026

Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
Published on: June 20, 2019
Alkylated cage silsesquioxane forming a long-range straight ordered hierarchical lamellar nanostructure
Lei Wang1, Yoshihito Ishida, Rina Maeda
1Department of Organic and Polymeric Materials, Tokyo Institute of Technology , Tokyo 152-8552, Japan.
Abstract:
An alkylated cage silsesquioxane (1), targeting for a new class of bottom-up-type fabricating materials, was successfully synthesized, and its self-assembled structure is described and discussed herein. Through this, it was found that the intermolecular interaction of long alkyl chains of 1 could be manipulated by thermal annealing to form a long-range straight ordered hierarchical lamellar structure with a periodicity of around 5 nm. Subsequent transmission electron microscopy (TEM) clearly identified polyhedral oligomeric silsesquioxane (POSS) molecules of 1 arranged in a highly ordered fashion, with a "head-to-head" type bilayered structure. The observation of a sublayer structure measuring approximately 0.4 nm in width was attributed to the highly regular packing of isobutyl groups in POSS molecules identified by TEM analysis. Moreover, the formation of a long-range straight structure with sharp interfacial boundaries, which is difficult to achieve with traditional diblock copolymers, is considered to be of significant importance to developing new practical applications of self-assembled nanostructures.
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