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Topochemical polymerization (TCP) emerges as a leading approach for synthesizing single crystalline polymers, but is traditionally restricted to transformations in solid-medium. The complexity in achieving single-crystal-to-single-crystal (SCSC) transformations due to lattice disparities and the untapped potential of performing TCP in a liquid medium with solid-state structural fidelity present unsolved challenges. Herein, by using X-rays as the primary means to overcome crystal disintegration, we reveal the details of SCSC transformation during the TCP of chiral azaquinodimethane (AQM) monomers through in situ crystallographic analysis while spotlighting a rare metastable crystalline phase. Complementary in situ investigations of powders and thin films provide critical insights into the side-chain dependent polymerization kinetics of solid-state reactions. Furthermore, we enable TCP of AQM monomers in a liquid medium via an antisolvent-reinforced aggregated state, yielding polymer nanofibers with high crystallinity akin to that of solid-state. This study testifies high structural precision of TCP performed in different states and media, offering critical insights into the synthesis of processable nanostructured polymers with desired structural integrity.
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http://dx.doi.org/10.1038/s41467-025-58822-2 | DOI Listing |
Carbohydr Polym
November 2025
Jiangsu Co-Innovation Center for Efficient Processing and Utilization of Forest Resources and International Innovation Center for Forest Chemicals and Materials, Nanjing Forestry University, Nanjing 210037, China. Electronic address:
Cellulose nanocrystals (CNCs) have garnered attention for their renewable and reactive nature, yet CNC allomorph II (CNC-II) remains underexplored compared to the extensively studied CNC-I. This study bridges this gap by introducing a two-step carboxylamine condensation strategy to conjugate poly(ethylene glycol) (PEG) onto CNC-II via ethylenediamine, leveraging the high topochemical reactivity of CNC-II. Utilizing bicarboxylate-capped PEG as a probe, quartz crystal microbalance with energy dissipation (QCM-D) assays revealed a significant reactivity increase of 16.
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September 2025
XStruct, Department of Chemistry, Ghent University, Krijgslaan-281, Building S3, B-9000 Ghent, Belgium.
Topochemical transformation in which the parent structural motifs are preserved has become a powerful strategy to access new advanced materials. Solid-state topochemical conversion in a single-crystal-to-single-crystal (SCSC) fashion is particularly attractive as it provides design principles with unequivocal structural details. Here, we report a series of two-dimensional (2D) lead-halide coordination polymers with bipyridyl ethylene (bpe) ligands that can undergo quantitative SCSC [2 + 2] photocycloaddition.
View Article and Find Full Text PDFBioresour Technol
December 2025
School of Energy and Chemical Engineering, Xiamen University Malaysia, 43900 Sepang, Selangor Darul Ehsan, Malaysia; Centre of Excellence for Industrial Research and Climate Action (CIRCLE), Xiamen University Malaysia, Selangor Darul Ehsan, Malaysia; College of Chemistry and Chemical Engineering, Xi
The acid-based approach for extracting nanocellulose supplies prfotons essential to hydrolyse cellulose and catalyse topochemical functionalization. However, the hydrolytic kinetics are so rapid that they cause the cellulose to degrade into monomeric sugars intractably, limiting the functionalization capacity. Thus, we posit a dual polyacid-based ternary deep eutectic solvent (DP/TDES), with incorporation of oxalic and citric acids that shifted the pronounced reactivity contribution from hydrolysis to H-bonding disruption mechanism.
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July 2025
Department of Chemistry and Biochemistry, University of Windsor 401 Sunset Avenue Windsor Ontario N9B 3P4 Canada
Semiconducting polymers have emerged as versatile, tunable materials for next-generation optoelectronic devices, offering advantages over traditional inorganic semiconductors in applications from energy harvesting to bioelectronics. Particularly, their compatibility with scalable manufacturing techniques, including solution-based deposition and printing methods, positions them favorably for commercial adoption. Among the recent strategies used to enhance the mechanical, thermal, and electronic properties of these polymers, crosslinking-through covalent or non-covalent interactions-has been shown to be especially efficient for improving their stability, robustness, and functionality.
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