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Biochemistry, molecular biology, biophysics, Biochimie, biologie moléculaire, biophysique, General chemistry, physical chemistry, Chimie générale, chimie physique, Nanotechnologies, nanostructures, nanoobjects, Nanotechnologies, nanostructures, nanoobjets, Polymers, paint and wood industries, Polymères, industries des peintures et bois, Sciences exactes et technologie, Exact sciences and technology, Chimie, Chemistry, Chimie generale et chimie physique, General and physical chemistry, Physicochimie de surface, Surface physical chemistry, Etat colloïdal et états dispersés, Colloidal state and disperse state, Matériaux poreux, Porous materials, Composé benzénique, Benzenic compound, Compuesto bencénico, Hydrocarbure, Hydrocarbon, Hidrocarburo, Acide, Acids, Acido, Autoassemblage, Self assembly, Autoensamble, Biphényle, Biphenyl, Bifenilo, Chimie, Chemistry, Química, Coadsorption, Coadsorción, Coronène, Coronene, Coroneno, Densité, Density, Densidad, Dimension, Dimensión, Formation image, Imaging, Formación imagen, Haute résolution, High resolution, Alta resolucion, Interface, Interfase, Liaison hydrogène, Hydrogen bond, Enlace hidrógeno, Matériau poreux, Porous material, Material poroso, Microscopie tunnel balayage, Scanning tunneling microscopy, Microscopía túnel barrido, Méthode fonctionnelle densité, Density functional method, Nanotechnologie, Nanotechnology, Nanotecnología, Pore, Poro, Solide, Solid, Sólido, Structure, and Estructura

Investigations of the self-assembly of simple molecules at the solution/solid interface can provide useful insight into the general principles governing supramolecular chemistry in two dimensions. Here, we report on the assembly of 3,4',5-biphenyl tricarboxylic acid (H3BHTC), a small hydrogen bonding unit related to the much-studied 1,3,5-benzenetricarboxylic acid (trimesic acid, TMA), which we investigate using scanning tunneling microscopy (STM) and density functional theory (DFT) calculations. STM images show that H3BHTC assembles by itself into an offset zigzag chain structure that maximizes the surface molecular density in favor of maximizing the number density of strong cyclic hydrogen bonds between the carboxylic groups. The offset geometry creates sticky pores that promote solvent coadsorption. Adding coronene to the molecular solution produces a transformation to a high-symmetry host―guest lattice stabilized by a dimeric/trimeric hydrogen bonding motif similar to the TMA flower structure. Finally, we show that the H3BHTC lattice firmly immobilizes the guest coronene molecules, allowing for high-resolution imaging of the coronene structure.

Biochemistry, molecular biology, biophysics, Biochimie, biologie moléculaire, biophysique, General chemistry, physical chemistry, Chimie générale, chimie physique, Nanotechnologies, nanostructures, nanoobjects, Nanotechnologies, nanostructures, nanoobjets, Polymers, paint and wood industries, Polymères, industries des peintures et bois, Sciences exactes et technologie, Exact sciences and technology, Physique, Physics, Domaines interdisciplinaires: science des materiaux; rheologie, Cross-disciplinary physics: materials science; rheology, Science des matériaux, Materials science, Matériaux particuliers, Specific materials, Fullerènes et matériaux apparentés; diamants, graphite, Fullerenes and related materials; diamonds, graphite, Chimie, Chemistry, Chimie generale et chimie physique, General and physical chemistry, Physicochimie de surface, Surface physical chemistry, Agent surface, Surfactants, Fullerènes, Fullerenes, Interface liquide liquide, Liquid liquid interface, Interfase líquido líquido, Nanobâtonnet, Nanorod, Nanopalito, Nanotechnologie, Nanotechnology, Nanotube, and Nanotubes

Herein we report the surfactant-triggered assembly of fullerene (C60) into 3D flowerlike microcrystals at the liquid-liquid interface. C60 crystals were grown using a liquid-liquid interfacial precipitation (LLIP) method by layering surfactant solution in butanol with a saturated solution of C60 in benzene. In the LLIP method, it is suggested that the crystal formation mechanism is driven by supersaturation related to the low C60 solubility in alcohol. We found that the dimensions of the synthesized C60 flowers depend on the concentration and surfactant type. In the absence of surfactant (i.e., in the butanol/benzene system), ID C60 nanowhiskers (nanorods) and C60 nanotubes (diameter 400 nm-2 μm and length 5-20 μm) are obtained. However, when surfactants are incorporated into the system flowerlike microcrystals consisting of C60 nanotubes are observed. For instance, crystals grown at the interface of a 0.01% diglycerol monolaurate (C12G2) nonionic surfactant in butanol with benzene lead to the formation of flower-shaped microcrystals of average sizes in the range of 10-35 μm. To the best of our knowledge, this is the first example of the surfactant-assisted assembly of C60 crystals. X-ray diffraction (XRD) and transmission electron microscopy (TEM) measurements have shown that fullerene flowers have a hexagonal structure with cell dimensions of a = 2.539 nm and c = 1.021 nm, which differ from that of pristine C60. Mixtures of flower-shaped C60 crystals and free-standing C60 nanotubes are found in the 0.1% C12G2/butanol system. However, clusters or giant aggregates of nanowhiskers lacking any specific shape are observed in the 1% C12G2/butanol system although these crystals exhibit hexagonal dose-packed structures. Flower-shaped C60 microcrystals are also observed with anionic surfactants cetyltrimethylammonium bromide (CTAB) and cetyltrimethylammonium chloride (CTAC). C60 flowers obtained from 0.01% CTAB and 0.01% CTAC also exhibit hexagonal structures with cell dimensions of a = 2.329 nm and c = 1.273 nm, a = 2.459 nm and c = 0.938 nm, respectively. Our C60 flowers exhibit intense photoluminescence (PL) and a blue-shifted PL intensity maximum compared to the same parameters for pristine C60, demonstrating the potential to control the optoelectronic properties of fullerene-based nanostructures.

Biochemistry, molecular biology, biophysics, Biochimie, biologie moléculaire, biophysique, General chemistry, physical chemistry, Chimie générale, chimie physique, Nanotechnologies, nanostructures, nanoobjects, Nanotechnologies, nanostructures, nanoobjets, Polymers, paint and wood industries, Polymères, industries des peintures et bois, Sciences exactes et technologie, Exact sciences and technology, Chimie, Chemistry, Chimie generale et chimie physique, General and physical chemistry, Physicochimie de surface, Surface physical chemistry, Etat colloïdal et états dispersés, Colloidal state and disperse state, Etudes physiques et chimiques. Granulométrie. Phénomènes électrocinétiques, Physical and chemical studies. Granulometry. Electrokinetic phenomena, Micelles. Lames minces, Micelles. Thin films, Composé de métal de transition, Transition element compounds, Acrylamide, Anticorps, Antibody, Anticuerpo, Antigène, Antigen, Antígeno, Chauffage, Heating, Calefacción, Copolymère statistique, Random copolymer, Copolímero estadístico, Copolymère séquencé, Block copolymer, Copolímero secuencia, Doxorubicine, Doxorubicin, Doxorubicina, Fonctionnalisation, Functionalization, Funciónalización, Formation image, Imaging, Formación imagen, Hydrophobicité, Hydrophobicity, Hidrofobicidad, Interface, Interfase, Libération, Release, Liberación, Micelle, Micela, Médicament, Drug, Medicamento, Nanoparticule, Nanoparticle, Nanopartícula, Nanotechnologie, Nanotechnology, Nanotecnología, Oxyde de fer, Iron oxide, Hierro óxido, Particule, Particle, Partícula, Polymère, Polymer, Polímero, Structure, Estructura, Superparamagnétisme, Superparamagnetism, Superparamagnetismo, Technologie avancée, Advanced technology, Tecnología avanzada, Application biomédicale, Biomedical application, Matériau fonctionnel, and Functional material

Hybrid nanoarchitectures are among the most promising nanotechnology-enabled materials for biomedical applications. Interfacing of nanoparticles with active materials gives rise to the structures with unique multiple functionality. Superparamagnetic iron oxide nanoparticles particles SPION are widely employed in the biology and in developing of advanced medical technologies. Polymeric micelles offer the advantage of multifunctional carriers which can serve as delivery vehicles carrying nanoparticles, hydrophobic chemotherapeutics and other functional materials and molecules. Stimuli-responsive polymers are especially attractive since their properties can be modulated in a controlled manner. Here we report on multifunctional thermo-responsive poly(N-isopropylacrylamide-co-acrylamide)-block-poly(ε-caprolactone) random block copolymer micelles as magnetic hyperthermia-mediated payload release and imaging agents. The combination of copolymers, nanoparticles and doxorubicin drug was tailored the way that the loaded micelles were cable to respond to magnetic heating at physiologically-relevant temperatures. A surface functionalization of the micelles with the integrin β4 antibody and consequent interfacing of the resulting nanobio hybrid with squamous head and neck carcinoma cells which is known to specifically over-express the A9 antigen resulted in concentration of the micelles on the surface of cells. No inherent cytotoxicity was detected for the magnetic micelles without external stimuli application. Furthermore, SPION-loaded micelles demonstrate significant MRI contrast enhancement abilities.

Biochemistry, molecular biology, biophysics, Biochimie, biologie moléculaire, biophysique, General chemistry, physical chemistry, Chimie générale, chimie physique, Nanotechnologies, nanostructures, nanoobjects, Nanotechnologies, nanostructures, nanoobjets, Polymers, paint and wood industries, Polymères, industries des peintures et bois, Sciences exactes et technologie, Exact sciences and technology, Chimie, Chemistry, Chimie generale et chimie physique, General and physical chemistry, Physicochimie de surface, Surface physical chemistry, Etat colloïdal et états dispersés, Colloidal state and disperse state, Etudes physiques et chimiques. Granulométrie. Phénomènes électrocinétiques, Physical and chemical studies. Granulometry. Electrokinetic phenomena, Germanium, Germanio, Interface, Interfase, Nanoparticule, Nanoparticle, Nanopartícula, Nanotechnologie, Nanotechnology, and Nanotecnología

It is revealed that rigorous control of the size and surface of germanium nanoparticles allows fine color tuning of efficient fluorescence emission in the visible region. The spectral line widths of each emission were very narrow (<500 meV). Furthermore, the absolute fluorescence quantum yields of each emission were estimated to be 4-15%, which are high enough to be used as fluorescent labeling tags. In this study, a violet-light-emitting nanoparticle is demonstrated to be a new family of luminescent Ge. Such superior properties of fluorescence were observed from the fractions separated from one mother Ge nanoparticle sample by the fluorescent color using our developed combinatorial column technique. It is commonly believed that a broad spectral line width frequently observed from Ge nanopartide appears because of an indirect band gap nature inherited even in nanostructures, but the present study argues that such a broad luminescence spectrum is expressed as an ensemble of different spectral lines and can be separated into the fractions emitting light in each wavelength region by the appropriate postsynthesis process.

Biochemistry, molecular biology, biophysics, Biochimie, biologie moléculaire, biophysique, General chemistry, physical chemistry, Chimie générale, chimie physique, Nanotechnologies, nanostructures, nanoobjects, Nanotechnologies, nanostructures, nanoobjets, Polymers, paint and wood industries, Polymères, industries des peintures et bois, Sciences exactes et technologie, Exact sciences and technology, Chimie, Chemistry, Chimie generale et chimie physique, General and physical chemistry, Physicochimie de surface, Surface physical chemistry, Autoassemblage, Self assembly, Autoensamble, Etat solide, Solid state, Estado sólido, Interface, Interfase, Liquide, Liquid, Líquido, Nanotechnologie, Nanotechnology, Nanotecnología, Solide, Solid, and Sólido

The self-assembly of small molecular modules interacting through noncovalent forces is increasingly being used to generate functional structures and materials for electronic, catalytic, and biomedical applications. The greatest control over the geometry in H-bond supramolecular architectures, especially in H-bonded supramolecular polymers, can be achieved by exploiting the rich programmability of artificial nucleobases undergoing self-assembly through strong H bonds. Here N3-functionalized xanthine modules are described, which are capable of self-associating through self-complementary H-bonding patterns to form H-bonded supramolecular ribbons. The self-association of xanthines through directional H bonding between neighboring molecules allows the controlled generation of highly compact ID supramolecular polymeric ribbons on graphite. These architectures have been characterized by scanning tunneling microscopy at the solid-liquid interface, corroborated by dispersion-corrected density functional theory (DFT) studies and X-ray diffraction.

Biochemistry, molecular biology, biophysics, Biochimie, biologie moléculaire, biophysique, General chemistry, physical chemistry, Chimie générale, chimie physique, Nanotechnologies, nanostructures, nanoobjects, Nanotechnologies, nanostructures, nanoobjets, Polymers, paint and wood industries, Polymères, industries des peintures et bois, Sciences exactes et technologie, Exact sciences and technology, Chimie, Chemistry, Chimie generale et chimie physique, General and physical chemistry, Physicochimie de surface, Surface physical chemistry, Autoassemblage, Self assembly, Autoensamble, Biotechnologie, Biotechnology, Biotecnología, Cholestérol, Cholesterol, Colesterol, Eau, Water, Agua, Enzyme, Enzima, Interface, Interfase, Lysine, Lisina, Nanogel, Nanotechnologie, Nanotechnology, Nanotecnología, Oligoside, Oligosaccharide, Oligósido, Polymère, Polymer, Polímero, Polymérisation, Polymerization, Polimerización, Polyoside, Polysaccharide, Poliósido, Polypeptide, Polipéptido, Structure, Estructura, Substitution, Substitución, and pH

In this study, we prepared a new associating polymer, ChMaPLL, by the substitution of the poly(L-lysine) moiety with oligosaccharide amylose primer and cholesterol. ChMaPLL formed positively charged polypeptide nanogels (∼50 nm) via self-assembly in water. The nanogels showed a secondary structural transition to an a-helix structure induced by poly(L-lysine) in response to an increase in pH. Oligosaccharides of the nanogels reacted with the phosphorylase a enzyme. Amylose-conjugated nanogels were obtained by enzymatic polymerization. The elongation of the saccharide chain shielded the positive charge of the nanogels. The multiresponsive polysaccharide-polypeptide hybrid nanogels might prove to be useful in the areas of biotechnology and biomedicine.

Biochemistry, molecular biology, biophysics, Biochimie, biologie moléculaire, biophysique, General chemistry, physical chemistry, Chimie générale, chimie physique, Nanotechnologies, nanostructures, nanoobjects, Nanotechnologies, nanostructures, nanoobjets, Polymers, paint and wood industries, Polymères, industries des peintures et bois, Sciences exactes et technologie, Exact sciences and technology, Chimie, Chemistry, Chimie generale et chimie physique, General and physical chemistry, Physicochimie de surface, Surface physical chemistry, Etat colloïdal et états dispersés, Colloidal state and disperse state, Etudes physiques et chimiques. Granulométrie. Phénomènes électrocinétiques, Physical and chemical studies. Granulometry. Electrokinetic phenomena, Métal transition, Transition metal, Metal transición, Interface, Interfase, Nanoparticule, Nanoparticle, Nanopartícula, Nanotechnologie, Nanotechnology, Nanotecnología, Or, Gold, Oro, Agent structurant, and Template

Ordered arrays of metal nanopartides are important for nanoelectronic and nanophotonic applications. Here, we report the formation of self-assembled arrays of gold nanoparticles on molecular layers of diacetylene compounds on a MoS2(0001) substrate. The arrangement of gold nanoparticles is observed using scanning tunneling microscopy. When gold is deposited on a self-assembled monolayer of 10,12-nonacosadiynoic acid or 10,12-octadecadiynoic acid on a MoS2(0001) substrate, the ordered array of diacetylene moieties in the molecular layer serves as a template for the formation of ordered arrays of gold nanoparticles. In contrast, when gold is deposited on a pristine MoS2(0001) surface or on a molecular layer of stearic acid, the gold nanoparticles are randomly distributed on the surface. It is found that the arrangement of gold nanoparticles is largely determined by the deposition rate; faster deposition results in more ordered arrays of gold nanoparticles. Our observations confirm the role of unsaturated π systems in molecules acting as a template for the regular arrangement of gold nanoparticles; this work will open up new possibilities for interfacial nanoarchitectonics.

Biochemistry, molecular biology, biophysics, Biochimie, biologie moléculaire, biophysique, General chemistry, physical chemistry, Chimie générale, chimie physique, Nanotechnologies, nanostructures, nanoobjects, Nanotechnologies, nanostructures, nanoobjets, Polymers, paint and wood industries, Polymères, industries des peintures et bois, Sciences exactes et technologie, Exact sciences and technology, Chimie, Chemistry, Chimie generale et chimie physique, General and physical chemistry, Physicochimie de surface, Surface physical chemistry, Adhésivité, Adhesivity, Adhesividad, Adsorption sélective, Selective adsorption, Adsorción selectiva, Alkylamine, Alquilamina, Amine, Amina, Couche bimoléculaire, Bilayer, Capa bimolecular, Croissance, Growth, Crecimiento, Dynamique moléculaire, Molecular dynamics, Dinámica molecular, Dynamique, Dynamics, Dinámica, Echelle nanométrique, Nanometer scale, Efficacité, Efficiency, Eficacia, Fibre, Fiber, Fibra, Film, Película, Garnissage, Packing, Relleno, Graphène, Graphene, Hydrophobicité, Hydrophobicity, Hidrofobicidad, Hydroxyle, Hydroxyl, Hidroxilo, Immobilisation, Immobilization, Inmovilización, Interface, Interfase, Liaison, Binding, Enlace, Modèle, Models, Modelo, Modélisation, Modeling, Modelización, Orientation, Orientación, Peptide, Peptides, Péptido, Physisorption, Fisisorción, Propriété mécanique, Mechanical properties, Propiedad mecánica, Propriété physicochimique, Physicochemical properties, Propiedad fisicoquímica, Protéine, Protein, Proteína, Simulation ordinateur, Computer simulation, Simulación computadora, Structure atomique, Atomic structure, Estructura atómica, Substrat, Substrate, Substrato, Couche monomoleculaire autoassemblée, Self-assembled monolayer, and Monocouche

Atomic-scale molecular dynamics computer simulations are used to probe the structure, dynamics, and energetics of alkylamine self-assembled monolayer (SAM) films on graphene and to model the formation of molecular bilayers and protein complexes on the films. Routes toward the development and exploitation of functionalized graphene structures are detailed here, and we show that the SAM architecture can be tailored for use in emerging applications (e.g., electrically stimulated nerve fiber growth via the targeted binding of specific cell surface peptide sequences on the functionalized graphene scaffold). The simulations quantify the changes in film physisorption on graphene and the alkyl chain packing efficiency as the film surface is made more polar by changing the terminal groups from methyl (-CH3) to amine (-NH2) to hydroxyl (-OH). The mode of molecule packing dictates the orientation and spacing between terminal groups on the surface of the SAM, which determines the way in which successive layers build up on the surface, whether via the formation of bilayers of the molecule or the immobilization of other (macro)molecules (e.g., proteins) on the SAM. The simulations show the formation of ordered, stable assemblies of monolayers and bilayers of decyiamine-based molecules on graphene. These films can serve as protein adsorption platforms, with a hydrophobin protein showing strong and selective adsorption by binding via its hydrophobic patch to methyl-terminated films and binding to amine-terminated films using its more hydrophilic surface regions. Design rules obtained from modeling the atomic-scale structure of the films and interfaces may provide input into experiments for the rational design of assemblies in which the electronic, physicochemical, and mechanical properties of the substrate, film, and protein layer can be tuned to provide the desired functionality.

Biochemistry, molecular biology, biophysics, Biochimie, biologie moléculaire, biophysique, General chemistry, physical chemistry, Chimie générale, chimie physique, Nanotechnologies, nanostructures, nanoobjects, Nanotechnologies, nanostructures, nanoobjets, Polymers, paint and wood industries, Polymères, industries des peintures et bois, Sciences exactes et technologie, Exact sciences and technology, Chimie, Chemistry, Chimie generale et chimie physique, General and physical chemistry, Physicochimie de surface, Surface physical chemistry, Interface solide-liquide, Solid-liquid interface, Etat colloïdal et états dispersés, Colloidal state and disperse state, Etudes physiques et chimiques. Granulométrie. Phénomènes électrocinétiques, Physical and chemical studies. Granulometry. Electrokinetic phenomena, Forme, Shape, Forma, Interface, Interfase, Microparticule, Microparticle, Micropartícula, Modification, Modificación, Morphologie, Morphology, Morfología, Mouillage, Wetting, Remojo, Nanotechnologie, Nanotechnology, Nanotecnología, Nanoflocon, and Nanoflake

Inducing a phase transition of a self-organized object may trigger its structural transformation. Here, we demonstrate local control of the morphology and shape of self-organized microparticles with a nanoflake outer surface by nanoplasmonic heating. To increase the photothermal efficiency of the microparticles, gold nanoparticles (AuNPs) or single-walled carbon nanotubes (SWCNTs) were incorporated. AuNPs and SWCNTs, which have excellent photothermal activity, acts as photoresponsive heat converters. Because they have distinct absorption characteristics, visible or near-infrared lasers can be used to induce local heating. The photothermal effect was used to spatially confine the melting to the space within the particle and the aggregate; as a result, microparticles with various shapes and morphologies have been fabricated. Such morphological changes lead to a superhydrophobic―hydrophobic wetting transition, which was confirmed by the films constituting the micropartides. The work presented is seen useful for anisotropic particle synthesis, local wetting control, lithography, and morphological control of functional materials.

Biochemistry, molecular biology, biophysics, Biochimie, biologie moléculaire, biophysique, General chemistry, physical chemistry, Chimie générale, chimie physique, Nanotechnologies, nanostructures, nanoobjects, Nanotechnologies, nanostructures, nanoobjets, Polymers, paint and wood industries, Polymères, industries des peintures et bois, Sciences exactes et technologie, Exact sciences and technology, Chimie, Chemistry, Chimie generale et chimie physique, General and physical chemistry, Physicochimie de surface, Surface physical chemistry, Etat colloïdal et états dispersés, Colloidal state and disperse state, Etudes physiques et chimiques. Granulométrie. Phénomènes électrocinétiques, Physical and chemical studies. Granulometry. Electrokinetic phenomena, Diffusion, Difusión, Eau, Water, Agua, Effet composition, Composition effect, Efecto composición, Huile, Oil, Aceite, Interface, Interfase, Nanoparticule, Nanoparticle, Nanopartícula, Nanotechnologie, Nanotechnology, Nanotecnología, Structure, and Estructura

Dissipative particle dynamics simulations are performed to study the structural and dynamical properties of various systems of nanoparticles accumulated at the water/oil interface. Homogeneous and Janus nanoparticles with different surface compositions are studied. For all nanoparticles, as the surface density increases, a transition from a liquidlike to a solidlike state is observed, as expected. At a high density of nanoparticles, hexagonal structures emerge and the nanoparticles' self-diffusion coefficient decreases because of caging effects. Similar results are observed for nanoparticles with different surface chemistry. Because different nanoparticles have different contact angles at the water/oil interface, the results obtained for systems containing mixed nanoparticles are more interesting. For example, our results show that the self-diffusion coefficient is not a monotonic function of the system composition, caused by the complex relation between hydrodynamic interactions and effective nanoparticle-nanoparticle interactions.

Biochemistry, molecular biology, biophysics, Biochimie, biologie moléculaire, biophysique, General chemistry, physical chemistry, Chimie générale, chimie physique, Nanotechnologies, nanostructures, nanoobjects, Nanotechnologies, nanostructures, nanoobjets, Polymers, paint and wood industries, Polymères, industries des peintures et bois, Sciences exactes et technologie, Exact sciences and technology, Chimie, Chemistry, Chimie generale et chimie physique, General and physical chemistry, Physicochimie de surface, Surface physical chemistry, Sciences appliquees, Applied sciences, Energie, Energy, Combustibles, Fuels, Combustibles de remplacement. Production et utilisation, Alternative fuels. Production and utilization, Hydrogène, Hydrogen, Fibre verre, Glass fiber, Fibra vidrio, Interface, Interfase, Nanotechnologie, Nanotechnology, Nanotecnología, Stockage hydrogène, Hydrogen storage, Support, Soporte, and Titanosilicate

This work reports on the synthesis of nanosheets of layered titanosilicate JDF-L1 supported on commercial E-type glass fibers with the aim of developing novel nanoarchitectures useful as robust and easy to handle hydrogen adsorbents. The preparation of those materials is carried out by hydrothermal reaction from the corresponding gel precursor in the presence of the glass support. Because of the basic character of the synthesis media, silica from the silicate-based glass fibers can be involved in the reaction, cementing its associated titanosilicate and giving rise to strong linkages on the support with the result of very stable heterostructures. The nanoarchitectures built up by this approach promote the growth and disposition of the titanosilicate nanosheets as a house-of-cards radially distributed around the fiber axis. Such an open arrangement represents suitable geometry for potential uses in adsorption and catalytic applications where the active surface has to be available. The content of the titanosilicate crystalline phase in the system represents about 12 wt %, and this percentage of the adsorbent fraction can achieve, at 298 K and 20 MPa, 0.14 wt % hydrogen adsorption with respect to the total mass of the system. Following postsynthesis treatments, small amounts of Pd (<0.1 wt %) have been incorporated into the resulting nanoarchitectures in order to improve their hydrogen adsorption capacity. In this way, Pd-layered titanosilicate supported on glass fibers has been tested as a hydrogen adsorbent at diverse pressures and temperatures, giving rise to values around 0.46 wt % at 298 K and 20 MPa. A mechanism of hydrogen spillover involving the titanosilicate framework and the Pd nanoparticules has been proposed to explain the high increase in the hydrogen uptake capacity after the incorporation of Pd into the nanoarchitecture.

Biochemistry, molecular biology, biophysics, Biochimie, biologie moléculaire, biophysique, General chemistry, physical chemistry, Chimie générale, chimie physique, Nanotechnologies, nanostructures, nanoobjects, Nanotechnologies, nanostructures, nanoobjets, Polymers, paint and wood industries, Polymères, industries des peintures et bois, Sciences exactes et technologie, Exact sciences and technology, Chimie, Chemistry, Chimie generale et chimie physique, General and physical chemistry, Physicochimie de surface, Surface physical chemistry, Etat colloïdal et états dispersés, Colloidal state and disperse state, Etudes physiques et chimiques. Granulométrie. Phénomènes électrocinétiques, Physical and chemical studies. Granulometry. Electrokinetic phenomena, Acide hyaluronique, Hyaluronic acid, Hialurónico ácido, Agrégation, Aggregation, Agregación, Chitosane, Chitosan, Quitosano, Couche multimoléculaire, Multilayer, Capa multimolecular, Diffusion lumière, Light scattering, Difusión luz, Dosage, Assay, Dosificación, Dynamique, Dynamics, Dinámica, Dégradation, Degradation, Degradación, Dépôt, Deposition, Depósito, Echelle nanométrique, Nanometer scale, Explosion, Explosions, Explosión, Glycol, Glicol, Interface, Interfase, Liaison, Binding, Enlace, Lysine, Lisina, Microscopie électronique transmission, Transmission electron microscopy, Microscopía electrónica transmisión, Modification, Modificación, Nanotechnologie, Nanotechnology, Nanotecnología, Particule enrobée, Coated particle, Partícula envuelta, Polymère, Polymer, Polímero, Potentiel surface, Surface potential, Potencial superficie, Potentiel électrocinétique, Electrokinetic potential, Potencial electrocinético, pH, Agent structurant, and Template

In this study, we created a nanoscale layer of hyaluronic acid (HA) on the inactivated Hemagglutinating Virus of Japan envelope (HVJ-E) via a layer-by-layer (LbL) assembly technique for CD-44 targeted delivery. HVJ-E was selected as the template virus because it has shown a tumor-suppressing ability by eliciting inflammatory cytokine production in dendritic cells. Although it has been required to increase the tumor-targeting ability and reduce nonspecific binding because HVJ-E fuses with virtually all cells and induces hemagglutination in the bloodstream, complete modifications of single-envelope-type viruses with HA have been difficult. Therefore, we studied the surface ζ potential of HVJ-E at different pH values and carefully examined the deposition conditions for the first layer using three cationic polymers: poly-L-lysine (PLL), chitosan (CH), and glycol chitosan (GC). GC-coated HVJ-E particles showed the highest disperse ability under physiological pH and salt conditions without aggregation. An HA layer was then prepared via alternating deposition of HA and GC. The successive decoration of multilayers on HVJ-E has been confirmed by dynamic light scattering (DLS), ζ potentials, and transmission electron microscopy (TEM). An enzymatic degradation assay revealed that only the outermost HA layer was selectively degraded by hyaluronidase. However, entire layers were destabilized at lower pH. Therefore, the HA/GC-coated HVJ-E describe here can be thought of as a potential bomb for cancer immunotherapy because of the ability of targeting CD44 as well as the explosion of nanodecorated HA/GC layers at endosomal pH while preventing nonspecific binding at physiological pH and salt conditions such as in the bloodstream or normal tissues.

Biochemistry, molecular biology, biophysics, Biochimie, biologie moléculaire, biophysique, General chemistry, physical chemistry, Chimie générale, chimie physique, Nanotechnologies, nanostructures, nanoobjects, Nanotechnologies, nanostructures, nanoobjets, Polymers, paint and wood industries, Polymères, industries des peintures et bois, Sciences exactes et technologie, Exact sciences and technology, Chimie, Chemistry, Chimie generale et chimie physique, General and physical chemistry, Physicochimie de surface, Surface physical chemistry, Interface solide-liquide, Solid-liquid interface, Angle contact, Contact angle, Angulo contacto, Dynamique, Dynamics, Dinámica, Eau, Water, Agua, Film, Película, Gouttelette, Droplet, Gotita, Hydrophobicité, Hydrophobicity, Hidrofobicidad, Interface, Interfase, Liquide, Liquid, Líquido, Microstructure, Microestructura, Microélectronique, Microelectronics, Microelectrónica, Morphologie, Morphology, Morfología, Mouillabilité, Wettability, Remojabilidad, Mouillage, Wetting, Remojo, Nanostructure, Nanoestructura, Nanotechnologie, Nanotechnology, Nanotecnología, Préparation, Preparation, Preparación, Rebond, Rebound, Rebote, Rugosité, Roughness, Rugosidad, Solide, Solid, Sólido, Structure géométrique, Geometrical structure, and Estructura geométrica

Designing geometrical structures is an effective route to tailoring the wettability of a surface. BN-based hierarchical nano- and microstructures, in particular, vertically aligned and randomly distributed tubes and cones, were synthesized and employed as a platform for studying the influence of surface morphology on their static and dynamic interactions with water droplets. The variation of the contact angle in different hierarchical BN films is attributed to the combined effects of surface roughness and partial liquid-solid contact at the interface. Moreover, the impact response of water droplets impinging on BN arrays with different wetting properties is distinct In the case of superhydrophobic films, the water droplet bounces off the surface several times whereas in less hydrophobic films it does not rebound and remains pinned to the surface. These results provide a facile route for the selective preparation of hierarchical BN nanostructure array films and a better understanding of their tunable water-repelling behavior, for which a number of promising applications in microelectronics and optics can be envisaged.

Biochemistry, molecular biology, biophysics, Biochimie, biologie moléculaire, biophysique, General chemistry, physical chemistry, Chimie générale, chimie physique, Nanotechnologies, nanostructures, nanoobjects, Nanotechnologies, nanostructures, nanoobjets, Polymers, paint and wood industries, Polymères, industries des peintures et bois, Sciences exactes et technologie, Exact sciences and technology, Chimie, Chemistry, Chimie generale et chimie physique, General and physical chemistry, Physicochimie de surface, Surface physical chemistry, Basse fréquence, Low frequency, Baja frecuencia, Electrode, Electrodes, Electrodo, Enzyme, Enzima, Film, Película, Glycérol, Glycerol, Glicerol, Impédance, Impedance, Impedancia, Interface, Interfase, Liquide, Liquid, Líquido, Nanotechnologie, Nanotechnology, Nanotecnología, Optimisation, Optimization, Optimización, Polyélectrolyte, Polyelectrolyte, Polielectrolito, Visualisation, Visualization, and Visualización

The control of molecular architectures has been exploited in layer-by-layer (LbL) films deposited on Au interdigitated electrodes, thus forming an electronic tongue (e-tongue) system that reached an unprecedented high sensitivity (down to 10-12 M) in detecting catechol Such high sensitivity was made possible upon using units containing the enzyme tyrosinase, which interacted specifically with catechol, and by processing impedance spectroscopy data with information visualization methods. These latter methods, including the parallel coordinates technique, were also useful for identifying the major contributors to the high distinguishing ability toward catechol. Among several film architectures tested, the most efficient had a tyrosinase layer deposited atop LbL films of alternating layers of dioctadecyldimethylammonium bromide (DODAB) and 1,2-dipalmitoyl-sn-3-glycero-fosfo-rac-(1-glycerol) (DPPG), viz., (DODAB/DPPG)5/DODAB/Tyr. The latter represents a more suitable medium for immobilizing tyrosinase when compared to conventional polyelectrolytes. Furthermore, the distinction was more effective at low frequencies where double-layer effects on the film/liquid sample dominate the electrical response. Because the optimization of film architectures based on information visualization is completely generic, the approach presented here may be extended to designing architectures for other types of applications in addition to sensing and biosensing.

Biochemistry, molecular biology, biophysics, Biochimie, biologie moléculaire, biophysique, General chemistry, physical chemistry, Chimie générale, chimie physique, Nanotechnologies, nanostructures, nanoobjects, Nanotechnologies, nanostructures, nanoobjets, Polymers, paint and wood industries, Polymères, industries des peintures et bois, Sciences exactes et technologie, Exact sciences and technology, Chimie, Chemistry, Chimie generale et chimie physique, General and physical chemistry, Théorie des réactions, cinétique générale. Catalyse. Nomenclature, documentation chimique, informatique chimique, Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry, Catalyse, Catalysis, Physicochimie de surface, Surface physical chemistry, Aimantation, Magnetization, Imanación, Bulle, Bubble, Ampolla, Champ extérieur, External field, Campo exterior, Champ magnétique, Magnetic field, Campo magnético, Interface, Interfase, Nanotechnologie, Nanotechnology, Nanotecnología, Nanotube, Nanotubo, Orientation, Orientación, Réaction catalytique, Catalytic reaction, and Reacción catalítica

Self-propelled catalytic bubble-ejecting nanotubes (nanojets) are expected to perform a variety of autonomous tasks. Herein, we will show that with the introduction of a Ni segment into the Au/Ni/Pt nanotube design followed by consequent magnetization a permanent change in the magnetic domain orientation of the Ni segment can be induced. Consequently, this results in the presence of a permanent magnet within the nanojet with its north/south domains oriented along the tube axis. Such a magnetized nanojet orients itself according to the external magnetic field and propels itself toward or away from the source of the magnetic field depending on its orientation. This behavior is similar to that of the magnetotactic bacteria. The ability to sense the magnetic field is expected to have a strong impact on future applications of autonomous self-propelled nanojets.

Biochemistry, molecular biology, biophysics, Biochimie, biologie moléculaire, biophysique, General chemistry, physical chemistry, Chimie générale, chimie physique, Nanotechnologies, nanostructures, nanoobjects, Nanotechnologies, nanostructures, nanoobjets, Polymers, paint and wood industries, Polymères, industries des peintures et bois, Sciences exactes et technologie, Exact sciences and technology, Chimie, Chemistry, Chimie generale et chimie physique, General and physical chemistry, Physicochimie de surface, Surface physical chemistry, Etat colloïdal et états dispersés, Colloidal state and disperse state, Etudes physiques et chimiques. Granulométrie. Phénomènes électrocinétiques, Physical and chemical studies. Granulometry. Electrokinetic phenomena, Absorption, Absorción, Agrégat, Aggregate, Agregado, Agrégation moléculaire, Molecular aggregation, Agregación molecular, Aire superficielle, Surface area, Area superficial, Amine secondaire, Secondary amine, Amina secundaria, Calcul, Calculation, Cálculo, Compression, Compresión, Densité, Density, Densidad, Diamètre, Diameter, Diámetro, Disque, Disk, Disco, Eau, Water, Agua, Epaisseur, Thickness, Espesor, Etalement, Spreading, Escalonamiento, Imide, Imida, Interface air eau, Air water interface, Interfase aire agua, Interface gaz liquide, Gas liquid interface, Interfase gas líquido, Isotherme, Isotherm, Isoterma, Liaison hydrogène, Hydrogen bond, Enlace hidrógeno, Mica, Microscopie force atomique, Atomic force microscopy, Microscopía fuerza atómica, Microstructure, Microestructura, Méthode Langmuir, Langmuir method, Método Langmuir, Méthodologie, Methodology, Metodología, Particule monodispersée, Monodispersed particle, Partícula monodispersada, Réflexion, Reflection, Reflexión, Solide, Solid, Sólido, Spectrométrie IR, Infrared spectrometry, Espectrometría IR, Structure, Estructura, Support, Soporte, Thermodynamique, Thermodynamics, Termodinámica, Monocouche, Nanodisque, and Nanodisk

In this article, we propose a novel methodology for the formation of monodisperse regularly sized disks of several nanometer thickness and with diameters of less than 100 nm using Langmuir monolayers as fabrication media. An amphiphilic triimide, tri-n-dodecylmellitic triimide (1), was spread as a monolayer at the air―water interface with a water-soluble macrocyclic oligoamine, 1,4,7,10-tetraazacyclododecane (cyclen), in the subphase. The imide moieties of 1 act as hydrogen bond acceptors and can interact weakly with the secondary amine moieties of cyclen as hydrogen bond donors. The monolayer behavior of 1 was investigated through π-A isotherm measurements and Brewster angle microscopy (BAM). The presence of cyclen in the subphase significantly shifted isotherms and induced the formation of starfish-like microstructures. Transferred monolayers on solid supports were analyzed by reflection absorption FT-IR (FT-IR-RAS) spectroscopy and atomic force microscopy (AFM). The Langmuir monolayer transferred onto freshly cleaved mica by a surface touching (i.e., Langmuir-Schaefer) method contained disk-shaped objects with a defined height of ca. 3 nm and tunable diameter in the tens of nanometers range. Several structural parameters such as the disk height, molecular aggregation numbers in disk units, and 2D disk density per unit surface area are further discussed on the basis of AFM observations together with aggregate structure estimation and thermodynamic calculations. It should be emphasized that these well-defined structures are produced through simple routine procedures such as solution spreading, mechanical compression, and touching a substrate at the surface. The controlled formation of defined nanostructures through easy macroscopic processes should lead to unique approaches for economical, energy-efficient nanofabrication.

Biochemistry, molecular biology, biophysics, Biochimie, biologie moléculaire, biophysique, General chemistry, physical chemistry, Chimie générale, chimie physique, Nanotechnologies, nanostructures, nanoobjects, Nanotechnologies, nanostructures, nanoobjets, Polymers, paint and wood industries, Polymères, industries des peintures et bois, Sciences exactes et technologie, Exact sciences and technology, Chimie, Chemistry, Chimie generale et chimie physique, General and physical chemistry, Physicochimie de surface, Surface physical chemistry, Caractérisation, Characterization, Caracterización, Carbone, Carbon, Carbono, Deutérium, Deuterium, Deuterio, Dissociation, Disociación, Echange proton, Proton exchange, Intercambio protón, Hydrogène, Hydrogen, Hidrógeno, Imide, Imida, Interaction intermoléculaire, Intermolecular interaction, Interacción intermolecular, Interface, Interfase, Nanomatériau, Nanostructured materials, Nanostructure, Nanoestructura, Nanotechnologie, Nanotechnology, Nanotecnología, Nanotube carbone, Carbon nanotubes, Nanotube monofeuillet, Singlewalled nanotube, Nanotubo pared única, Protéine, Protein, Proteína, Remplacement, Replacement, Reemplazo, Stabilité, Stability, Estabilidad, Structure, Estructura, Substitution, Substitución, and pH

Isotopic, hydrogen-to-deuterium substitution has been an invaluable tool in the characterization of small molecules and biological nanostructures. The natural variability of most inorganic nanomaterials has hindered the use of isotopic substitution in gaining meaningful insights into their structure. The ideal helical wrapping of a flavin mononucleotide (FMN) around (8,6)-SWNTs (single-walled carbon nanotubes) is presently utilized to probe isotopically dependent intermolecular interactions. The facile proton-to-deuterium exchange of the imide group of FMN enabled us to alter the intermolecular stability of the helix depending on the surrounding solvent (i.e., H2O vs D2O). Our studies show that FMN-dispersed (8,6)-SWNTs exhibit greater stability in D2O than in H2O. The higher complex stability in D2O was verified on the basis of (i) FMN helix replacement with SDBS (sodium dodecylbenzenesulfate) and (ii) thermal- and (iii) pH-induced helix dissociation. This is in agreement with the previously observed stronger amide H-bonding of proteins in D2O, and to the best of our knowledge, it demonstrates the architectural fidelity of FMN-wrapped SWNTs, which is expected to enhance the assembly repertoire of carbon nanotubes further.

Biochemistry, molecular biology, biophysics, Biochimie, biologie moléculaire, biophysique, General chemistry, physical chemistry, Chimie générale, chimie physique, Nanotechnologies, nanostructures, nanoobjects, Nanotechnologies, nanostructures, nanoobjets, Polymers, paint and wood industries, Polymères, industries des peintures et bois, Sciences exactes et technologie, Exact sciences and technology, Chimie, Chemistry, Chimie generale et chimie physique, General and physical chemistry, Physicochimie de surface, Surface physical chemistry, Argile, Clay, Arcilla, Corrosion, Corrosión, Inhibiteur, Inhibitor, Inhibidor, Interface, Interfase, Libération, Release, Liberación, Modification, Modificación, Nanotechnologie, Nanotechnology, Nanotecnología, Nanotube, and Nanotubo

Long-lasting anticorrosive coatings for steel have been developed on the basis of halloysite nanotubes loaded with three corrosion inhibitors: benzotriazole, mercaptobenzothiazole, and mercaptobenzimidazole. The inhibitors' loaded tubes were admixed at 5-10 wt % to oil-based alkyd paint providing sustained agent release and corrosion healing in the coating defects. The slow 20-30 h release of the inhibitors at defect points caused a remarkable improvement in the anticorrosion efficiency of the coatings. Further time expansion of anticorrosion agent release has been achieved by the formation of release stoppers at nanotube ends with ureaformaldehyde copolymer and copper-inhibitor complexation. The corrosion protection efficiency was tested on ASTM A366 steel plates in a 0.5 M NaCl solution with the microscanning of corrosion current development by microscopy inspection and studying paint adhesion. The best protection was found using halloysite/mercaptobenzimidazole and benzotriazole inhibitors. Stopper formation with urea―formaldehyde copolymer provided an additional increase in corrosion efficiency as a result of the longer release of inhibitors.

Biochemistry, molecular biology, biophysics, Biochimie, biologie moléculaire, biophysique, General chemistry, physical chemistry, Chimie générale, chimie physique, Nanotechnologies, nanostructures, nanoobjects, Nanotechnologies, nanostructures, nanoobjets, Polymers, paint and wood industries, Polymères, industries des peintures et bois, Sciences exactes et technologie, Exact sciences and technology, Chimie, Chemistry, Chimie generale et chimie physique, General and physical chemistry, Physicochimie de surface, Surface physical chemistry, Etat solide, Solid state, Estado sólido, Interface, Interfase, Lithium, Litio, Nanotechnologie, Nanotechnology, and Nanotecnología

Strong demand for solid-state lithium batteries has prompted intensive research for achieving fast ionic conduction in solids. Although the highest conductivity found among sulfides is higher than that of liquid electrolytes, it improves the battery performance only in combination with electrodes via a low-resistance interface. This Article reviews some interfacial structures that lower the interfacial resistance to enable high-power interfaces by controlling the carrier density.

Biochemistry, molecular biology, biophysics, Biochimie, biologie moléculaire, biophysique, General chemistry, physical chemistry, Chimie générale, chimie physique, Nanotechnologies, nanostructures, nanoobjects, Nanotechnologies, nanostructures, nanoobjets, Polymers, paint and wood industries, Polymères, industries des peintures et bois, Sciences exactes et technologie, Exact sciences and technology, Chimie, Chemistry, Chimie generale et chimie physique, General and physical chemistry, Physicochimie de surface, Surface physical chemistry, Conversion, Conversión, Energie, Energy, Energía, Interface, Interfase, Nanotechnologie, Nanotechnology, Nanotecnología, Nanomédecine, and Nanomedicine

Materials nanoarchitectonics has led to important innovations in the design and construction of systems in nanoelectronics, nanomachinery, and energy conversion. Recent publications point to the fact that the same approach may be applied successfully to other fields. In this Perspective, we define the key features of materials nanoarchitectonics and examine how they can be used to address current challenges in nanomedicine, placing emphasis on colloidal agents for therapeutic and diagnostic applications.