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Self-Assembly of Low-Molecular-Weight Asymmetric Linear Triblock Terpolymers: How Low Can We Go?

The synthesis of two (2) novel triblock terpolymers of the ABC type and one (1) of the BAC type, where A, B and C are chemically different segments, such as polystyrene (PS), poly(butadiene) (PB(1,4)) and poly(dimethylsiloxane) (PDMS), is reported; moreover, their corresponding molecular and bulk ch...

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Detalles Bibliográficos
Autores principales: Miskaki, Christina, Moutsios, Ioannis, Manesi, Gkreti-Maria, Artopoiadis, Konstantinos, Chang, Cheng-Yen, Bersenev, Egor A., Moschovas, Dimitrios, Ivanov, Dimitri A., Ho, Rong-Ming, Avgeropoulos, Apostolos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7728154/
https://www.ncbi.nlm.nih.gov/pubmed/33255708
http://dx.doi.org/10.3390/molecules25235527
Descripción
Sumario:The synthesis of two (2) novel triblock terpolymers of the ABC type and one (1) of the BAC type, where A, B and C are chemically different segments, such as polystyrene (PS), poly(butadiene) (PB(1,4)) and poly(dimethylsiloxane) (PDMS), is reported; moreover, their corresponding molecular and bulk characterizations were performed. Very low dimensions are evident from the characterization in bulk from transmission electron microscopy studies, verified by small-angle X-ray data, since sub-16 nm domains are evident in all three cases. The self-assembly results justify the assumptions that the high Flory–Huggins parameter, χ, even in low molecular weights, leads to significantly well-ordered structures, despite the complexity of the systems studied. Furthermore, it is the first time that a structure/properties relationship was studied for such systems in bulk, potentially leading to prominent applications in nanotechnology and nanopatterning, for as low as sub-10 nm thin-film manipulations.