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Capillarity driven self-assembly is a way to create spontaneous structures along liquid interfaces in between bottom-up and top-down fabrication methods. Based on multipolar capillary interactions between elementary floating object, simple to complex structures can been achieved by designing objects with specific 3D shapes. We show herein that a switchable self-assembled structure can be obtained with a shape memory polymer. At a defined temperature of the liquid, the 3D shape of each elementary floating object changes, modifying the capillary interactions thus forcing the stable structure to disassemble and to form a new arrangement. Based on simulations and experiments, we study how this cooperative behavior induces metastable complex configurations.
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http://dx.doi.org/10.1039/d0sm01251c | DOI Listing |
Langmuir
September 2025
Polymer Research Institute, State Key Laboratory of Advanced Polymer Materials, Sichuan University, Chengdu 610065, China.
Switchable surfactants exhibit broad application potential due to their reversible response to external stimuli. The reversible mechanism of the CO-switchable surfactant ('-dodecyl-, -dimethyl-acetamidines, DDA) solubilization polycyclic aromatic hydrocarbons (PAHs) and the microscopic dynamic behavior of emulsification/demulsification were systematically studied using coarse-grained molecular dynamics simulations. The dynamic transition processes of protonation (DDA to DDA) and deprotonation (DDA to DDA) were successfully simulated.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, 350002, P.R. China.
Photoswitchable catalysis presents a significant challenge, particularly in the modulation of reaction pathways. In this study, we describe a redox-active lanthanide-organic tetrahedral cage 1, self-assembled from a viologen-functionalised ditopic tridentate ligand and Eu(III) ions. Complexation-induced charge redistribution and spatial rearrangement of ligands in the assembly endow 1 with distinct photochromic properties and redox activities compared to free ligand L.
View Article and Find Full Text PDFJ Am Chem Soc
June 2025
Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu 610041, China.
Reductive elimination of dialkyl Ni(II) species for the enantioselective construction of a C(sp)-C(sp) bond represents a fundamental challenge due to the low oxidative ability of the Ni(II) ion. Here we report that a Ni(0) complex can perform as a π-Lewis base to activate the 2,4-dienoic carboxylate salts formed in situ with zinc reagents, such as dimethylzinc, and undergo vinylogous addition to carbonyls α-regioselectively and stereoselectively. After transmetalation with another organometallic reagent, the resultant alkyl allylic nickel(II) species readily undertake reductive elimination to finally forge two C(sp)-C(sp) bonds, even with switchable diastereodivergence and α,β- or α,δ-regiodivergence via ligand or substrate control.
View Article and Find Full Text PDFACS Appl Mater Interfaces
May 2025
Chemical Biology Unit, Institute of Nano Science and Technology, Sector-81, Mohali, Punjab 140306, India.
Exfoliated 2D transition-metal dichalcogenide (TMDCs)-based nanomaterials have captured a huge biomedical territory owing to their supreme physicochemical properties. However, the tedious and harsh chemical exfoliation of bulk MoS impacts its utility in the biological domain. The study introduces a facile and environmentally benign way of shape-tunable exfoliation of bulk MoS materials in an aqueous dispersion using designed self-assembled, tetrapeptide (Fmoc-HCKF-OH)-based nanostructures, generating hybrid MoS-peptide nanosystems for both tumor-targeted [employing folic acid (FA) functionalization] and NIR-responsive delivery of anticancer siRNA/drug in glioma.
View Article and Find Full Text PDFAdv Colloid Interface Sci
August 2025
Chemical and Environmental Engineering, School of Engineering, RMIT University, Melbourne, VIC 3000, Australia. Electronic address:
The applications of responsive biomaterials for tuning cell-surface interactions have been recently explored due to their unique switchable characteristics. However, rational design of surfaces using suitable biomacromolecules to attain optimal physicochemical performance, biocompatibility, cell adhesion and anti-fouling properties is quite challenging. Resilin-mimetic polypeptides (RMPs) are intrinsically disordered biomacromolecules that exhibit multi-stimuli responsive behaviour, including reversible dual-phase thermal behaviour forming self-assembled nano- to microstructures.
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