Cellulose nanocrystal (CNC) fillers have been shown to significantly improve the performance of polymer composites and hydrogels, elevating both strength and toughness. Polymer grafting from the surface of the nanocrystals has been employed to enhance matrix-filler interactions and keep the fillers dispersed within the matrix. However, such approaches often rely on multistep syntheses and diligent process control. Here, we propose modifying the nanocrystal surface to carry vinyl moieties, turning the particles into cross-linking comonomers. Using allyl glycidyl ether in an aqueous modification route, we were able to decorate the CNCs with varying amounts of vinyl moieties. Subsequent dispersion in 2-hydroxy methacrylate and thermally initiated free radical polymerization yielded composite materials that showed superior mechanical performance compared to those obtained from monomeric cross-linkers and unmodified CNCs. The large discrepancies in the observed glass transition temperatures of the obtained materials suggest, however, that the impact of the fillers on the polymerization kinetics is significant and less easily explained.
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http://dx.doi.org/10.1021/acs.biomac.4c01619 | DOI Listing |
Biomacromolecules
March 2025
Department of Bioproducts and Biosystems, Aalto University, Aalto FI-00076, Finland.
Cellulose nanocrystal (CNC) fillers have been shown to significantly improve the performance of polymer composites and hydrogels, elevating both strength and toughness. Polymer grafting from the surface of the nanocrystals has been employed to enhance matrix-filler interactions and keep the fillers dispersed within the matrix. However, such approaches often rely on multistep syntheses and diligent process control.
View Article and Find Full Text PDFChem Commun (Camb)
March 2025
Laboratory of Functional Molecular Solids, Ministry of Education, School of Chemistry and Materials Science, Anhui Normal University, Wuhu 241002, China.
An efficient and transition-metal-free method for the synthesis of unprecedented vinyl chloride-substituted BODIPYs has been developed through tandem Friedel-Crafts, enolization and chlorination reactions. This transformation offers high regioselectivity and stereoselectivity, enabling the synthesis of a variety of β-vinyl chloride-β'-acyl- and β,β'-divinyl chloride-substituted BODIPYs in a one-pot reaction at room temperature. Further functionalization gave a β,β'-divinyl chloride-substituted BODIPY with triphenyl phosphonium moieties, which showed favorable two-photon mitochondrion-targeting imaging capacity in living cells with intense deep-red fluorescence.
View Article and Find Full Text PDFChemistry
March 2025
Department of Organic Chemistry, Indian Institute of Science, Bangalore, 560012, Karnataka, India.
Transformation of the allyl glycosides to a glycosylation-active 3-thiocresyl-prop-1-enyl (TCP) glycosides is reported herein, in an effort to devise a shelf-stable, active vinyl glycoside. Remote electrophilic activation with an iodonium source results in the formation of a glycosylation-active moiety. The efficiency of the TCP glycoside donor is demonstrated through the synthesis of a panel of di- and trisaccharides of pyranosides and furanosides, including globo-trioside Gb antigen, wherein a disarmed TCP glycoside is converted facile to an armed TCP glycosyl donor, further ascertaining the tolerance towards protecting group manipulations.
View Article and Find Full Text PDFOrg Lett
March 2025
Department of Applied Chemistry, Graduate School of Engineering, Ehime University, 3 Bunkyo-cho, Matsuyama, Ehime 790-8577, Japan.
New derivatives of [4]dendralene with redox-active 1,3-dithiol-2-ylidene units were synthesized. X-ray crystal structure analysis of the dibenzo-tetramethyl derivative revealed that the molecule takes a conformation in which two vinyl-extended TTF moieties are significantly inclined to each other. The octamethyl derivative underwent cyclization with skeletal rearrangement in the dicationic state to give the corresponding dicationic trimethylenecylopentene, which exhibited a simultaneous two-electron reduction wave at a significantly negative potential of -0.
View Article and Find Full Text PDFEur J Med Chem
April 2025
Department of Chemical, Biological, Pharmaceutical, and Environmental Sciences, University of Messina, Viale Stagno d'Alcontres 31, 98166, Messina, Italy.
In this structure-activity relationship (SAR) study, we report the development of rhodesain-targeting peptidomimetics with antitrypanosomal activity. The new compounds (SPR65-SPR80) feature the 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (Tic) moiety as conformationally constrained Phe analog. Various substituents were inserted at the P1 and P3 positions, and the methyl vinyl ketone moiety was introduced as warhead.
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