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The morphological structures in thin films of a diblock copolymer of methyl methacrylate and polyhedral oligomeric silsesquioxane (POSS) functionalized methacrylate (PMMA-b-PMAPOSS) with a volume ratio of 13/87 were investigated in detail by using synchrotron grazing incidence small and wide-angle X-ray scattering (GISAXS and GIWAXS). In addition, its thermal properties were studied. Thin films of this diblock copolymer were found to undergo phase-separation during solvent-annealing with carbon disulfide and post thermal annealing. To quantitatively analyze the scattering data, GISAXS and GIWAXS formulas were derived and applied. Our detailed analysis found that cylinders of PMMA blocks are induced to form in the diblock copolymer films by solvent-annealing and are hexagonally packed in the PMAPOSS matrix, in which the cylinders are oriented vertically with respect to the film plane. In the solvent-annealed films, both the PMMA cylinders and the PMAPOSS matrix are featureless, i.e., amorphous. However, the post thermal annealing process induces aggregation of the POSS moieties, which results in the formation of crystals with an orthorhombic lattice unit cell. These crystals were found to consist of PMAPOSS block chains in a helical conformation in which the molecular PMAPOSS cylinders are aligned in the film plane. The formation of these crystals is induced by the ordering ability of the POSS moieties. The crystals were found to melt above 190 degrees C during heating and subsequent cooling. In contrast, the hexagonally packed structure of the PMMA cylinders in the solvent-annealed and post thermally annealed films was found to be retained during the heating and the subsequent cooling. In addition, the scattering analysis provides detailed structural parameters. The 2D GISAXS and GIWAXS patterns were reconstructed from the determined structural parameters by using the derived scattering formulas, and found to be in good agreement with the experimental patterns. Moreover, a model for the structure of the films of the diblock copolymer is proposed.
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http://dx.doi.org/10.1021/jp1008785 | DOI Listing |
J Chem Phys
September 2025
Department of Physics and Astronomy and Stewart Blusson Quantum Matter Institute, University of British Columbia, Vancouver, British Columbia V6T 1Z1, Canada.
Polymer dynamics is analyzed through the lens of linear dimensionality reduction methods, in particular principal and time-lagged independent component analysis (tICA). For a polymer undergoing ideal Rouse dynamics, the slow modes identified by these transformations coincide with the conventional Rouse modes. When applied to the Fourier modes of the segment density, we show that tICA generates dynamics equivalent to dynamic self-consistent field theory (D-SCFT) with a wavevector-dependent Onsager coefficient and a free energy functional subject to the random phase approximation.
View Article and Find Full Text PDFAnal Chem
September 2025
Department of Applied Chemistry, Faculty of Science and Technology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.
In this Article, we present a novel data analysis method for the determination of copolymer composition from low-resolution mass spectra, such as those recorded in the linear mode of time-of-flight (TOF) mass analyzers. Our approach significantly extends the accessible molecular weight range, enabling reliable copolymer composition analysis even in the higher mass regions. At low resolution, the overlapping mass peaks in the higher mass range hinder a comprehensive characterization of the copolymers.
View Article and Find Full Text PDFSmall
September 2025
South China Advanced Institute for Soft Matter Science and Technology, School of Emergent Soft Matter, Guangdong Provincial Key Laboratory of Functional and Intelligent Hybrid Materials and Devices, Guangdong Basic Research Center of Excellence for Energy and Information Polymer Materials, South Chi
Self-assembled poly(2-dimethylaminoethyl methacrylate)-poly(2-(diisopropylamino)ethyl methacrylate) (PDMA-PDPA) diblock copolymer nanoparticles are widely employed in biological applications, driving the need for a robust and scalable production method. Although polymerization-induced self-assembly (PISA) enables efficient nanoparticle synthesis at high solids content, its research and application to PDMA-PDPA are limited, likely due to kinetic trapping. Leveraging our recently developed generic time-resolved small-angle X-ray scattering (TR-SAXS) approach for PISA in non-polar media, a reversible addition-fragmentation chain transfer-mediated PDMA-PDPA PISA process in polar solvent that produces spherical micelles is examined.
View Article and Find Full Text PDFJ Mater Chem B
September 2025
The Avram and Stella Goldstein Goren Department of Biotechnology Engineering, Ben-Gurion University of the Negev, P.O.B. 653, Beer-Sheva 8410501, Israel.
The development of "smart" polymers capable of responding to physiologically relevant stimuli is essential for engineering dynamic sensing and actuation systems that leverage biological signals under specific (patho)physiological conditions. In this study, we present a general and versatile strategy to engineer novel stimuli-responsive behaviors in temperature-responsive protein-based polymers (PBPs) site-specific conjugation with self-immolative molecules. Specifically, we developed hydrogen peroxide (HO)- and β-galactosidase (β-gal)-responsive elastin-like polypeptides (ELPs) and resilin-like polypeptides (RLPs).
View Article and Find Full Text PDFACS Macro Lett
September 2025
Department of Chemistry, Yonsei University, Seoul 03722, Republic of Korea.
Alkyne groups provide exceptional versatility for functionalization in macromolecular systems. However, the controlled anionic ring-opening polymerization (AROP) of epoxide monomers bearing terminal alkynes remains challenging due to the lability of alkynes under strongly basic conditions. Herein, we present a controlled AROP of glycidyl propargyl ether enabled by Lewis pair organocatalysis, employing a phosphazene base and triethylborane.
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