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We successfully synthesized hyperbranched poly(triazole)s by in situ click polymerization of diazides 1 and triyne 2 monomers on different metal surfaces (copper, iron, and aluminum) and characterized their adhesive properties. Optimizations were performed to obtain high adhesive strength at different temperatures by analyzing the effects of curing kinetics, annealing temperature and time, catalyst, monomer ratio, surface conditions, alkyl chain length of diazides 1, etc. The adhesive bonding strength with metal substrate is 2 orders of magnitude higher than similar hyperbranched poly(triazole)s made by click polymerization and clearly higher than some commercial adhesives at elevated temperatures. With the same conditions, adhesives prepared on aluminum and iron substrates have higher adhesive strength than those prepared on copper substrate, and an excess of triyne 2 monomer in synthesis has greater adhesive strength than an excess of diazide 1 monomer. Tof-SIMS experiment was employed to understand these phenomena, and the existence of an interphase between the polymer and metal surface was found to be critical for adhesive bonding with thicker interphase (excess of triyne 2 monomer) and the higher binding energy between polymer atoms and substrate atoms (e.g., aluminum substrate) generating the higher bonding strength. In addition, the light-emitting property of synthesized polymers under UV irradiation can be used to check the failure mode of adhesive bonding.
ACS Appl Mater Interfaces 2010 Feb
PMID:Synthesis and curing of hyperbranched poly(triazole)s with click polymerization for improved adhesion strength. 2035 6

Self-assembled monolayers (SAMs) of iron oxide nanoparticles have been prepared using carboxylic-acid-terminated dendrimers. The iron-containing SAM was used as the catalyst for growth of vertical arrays of carbon nanotubes (CNTs). This approach has the potential for producing diameter controlled CNTs from premade catalyst nanoparticles as well as large scale production of CNTs by chemical vapor deposition.
ACS Appl Mater Interfaces 2010 Jan
PMID:Dendrimer-assisted self-assembled monolayer of iron nanoparticles for vertical array carbon nanotube growth. 2035 14

Ionic liquid (IL)-coated iron oxide nanoparticles (IONs) were synthesized by the thermal decomposition of Fe(CO)(5) in an IL/DMF solvent system in the absence of stabilizing surfactants at 90 degrees C for 1 h. The IL, [omim][BF(4)], could regulate the shape and allow the preparation of anisotropic IONs, such as barlike and wirelike nanoparticles. The barlike IONs prepared using this method showed good superparamagnetic behavior in a magnetic field and a MR contrast enhancement effect in a MR scanner.
ACS Appl Mater Interfaces 2010 Mar
PMID:Synthesis of iron oxide nanoparticles with control over shape using imidazolium-based ionic liquids. 2035 77

We report the preparation of alpha-Fe2O3 electrodes using a technique known as reactive ballistic deposition in which iron metal is evaporatively deposited in an oxygen ambient for photoelectrochemical (PEC) water oxidation. By manipulating synthesis parameters such as deposition angle, film thickness, and annealing temperature, we find that it is possible to optimize the structural and morphological properties of such films in order to improve their PEC efficiency. Incident photon to current conversion efficiencies (IPCE) are used to calculate an AM1.5 photocurrent of 0.55 mA/cm(2) for optimized films with an IPCE reaching 10% at 420 nm in 1 M KOH at +0.5 V versus Ag/AgCl. We also note that the commonly observed low photoactivity of extremely thin hematite films on fluorine-doped tin oxide substrates may be improved by modification of annealing conditions in some cases.
ACS Nano 2010 Apr 27
PMID:Reactive ballistic deposition of alpha-Fe2O3 thin films for photoelectrochemical water oxidation. 2036 56

Growing evidence points toward a very dynamic role for metals in biology. This suggests that physiological circumstance may mandate metal ion redistribution among ligands. This work addresses a critical need for technology that detects, identifies, and measures the metal-containing components of complex biological matrixes. We describe a direct, user-friendly approach for identifying and quantifying metal-protein adducts in complex samples using native- or SDS-PAGE, blotting, and rapid synchrotron X-ray fluorescence mapping with micro-XANES (X-ray absorption near-edge structure) of entire blots. The identification and quantification of each metal bound to a protein spot has been demonstrated, and the technique has been applied in two exemplary cases. In the first, the speciation of the in vitro binding of exogenous chromium to blood serum proteins was influenced markedly by both the oxidation state of chromium exposed to the serum proteins and the treatment conditions, which is of relevance to the biochemistry of Cr dietary supplements. In the second case, in vivo changes in endogenous metal speciation were examined to probe the influence of oxygen depletion on iron speciation in Shewanella oneidensis.
ACS Chem Biol 2010 Jun 18
PMID:Imaging metals in proteins by combining electrophoresis with rapid x-ray fluorescence mapping. 2055 40

Precious metals supported on ferrimagnetic particles have a diverse range of uses in catalysis. However, fabrication using synthetic methods results in potentially high environmental and economic costs. Here we show a novel biotechnological route for the synthesis of a heterogeneous catalyst consisting of reactive palladium nanoparticles arrayed on a nanoscale biomagnetite support. The magnetic support was synthesized at ambient temperature by the Fe(III)-reducing bacterium, Geobacter sulfurreducens , and facilitated ease of recovery of the catalyst with superior performance due to reduced agglomeration (versus conventional colloidal Pd nanoparticles). Surface arrays of palladium nanoparticles were deposited on the nanomagnetite using a simple one-step method without the need to modify the biomineral surface, most likely due to an organic coating priming the surface for Pd adsorption, which was produced by the bacterial culture during the formation of the nanoparticles. A combination of EXAFS and XPS showed the Pd nanoparticles on the magnetite to be predominantly metallic in nature. The Pd(0)-biomagnetite was tested for catalytic activity in the Heck reaction coupling iodobenzene to ethyl acrylate or styrene. Rates of reaction were equal to or superior to those obtained with an equimolar amount of a commercial colloidal palladium catalyst, and near complete conversion to ethyl cinnamate or stilbene was achieved within 90 and 180 min, respectively.
ACS Nano 2010 May 25
PMID:Microbial engineering of nanoheterostructures: biological synthesis of a magnetically recoverable palladium nanocatalyst. 2039 56

Nanohybrids with magnetic iron-oxide nanoparticles (FeNPs) embedded in the multilayered silicate clay were synthesized by in situ Fe(2+)/Fe(3+) coprecipitation. The natural clay, sodium montmorillonite (Na(+)-MMT), was first modified with hydrophobic poly(oxypropylene)amine salts (POP at 2000 and 4000 g/mol M(w)). The two POP-intercalated organoclays, with a silicate interlayer expansion from 1.2 to 5.2 and 9.2 nm, respectively, are suitable for embedding FeNPs. The presence of POP organics in layered structure created the space for intercalating with FeNPs of 2-4 nm in diameter, observed by transmission electronic microscope. The synthesized nanohybrids of POP4000/MMT-FeNP was composed of 17% iron oxide and 51 wt % POP within the silicate basal spacing of 5.0 nm. In contrast, the lower molecular weight of POP2000 intercalated MMT failed to encapsulate FeNPs in a significant amount, but resulting a "crowding-out effect" that caused the silicate interlayer space to shrink from 5.2 to 1.8 nm because of the replacement of the POP salt by Fe(2+)/Fe(3+) ions. The synthesis required the use of high molecular weight POP4000 and low temperatures (<4 degrees C) for a better dispersion in the reaction medium. The presence of POP in the layered silicate facilitated a homogeneous POP/MMT in water, associating with Fe(2+)/Fe(3+) ions and spatially accommodating for the subsequently generated FeNPs. The synthesized nanostructure consisting of POP and FeNP could be used as a pollutant remedy because of its ability to adsorbing crude oil and it is maneuverable under an applied magnetism.
ACS Appl Mater Interfaces 2010 May
PMID:Nanohybrids of magnetic iron-oxide particles in hydrophobic organoclays for oil recovery. 2040 92

We evaluate the potential in vitro cytotoxicity that may arise from metallic and magnetic DNA-templated nanostructures. By using a fluorescence-based assay, the viability of cells was examined after treatment with DNA-templated nanostructures. Inductively coupled plasma mass spectrometry (ICP-MS) was used to quantify the amount of nanoparticles internalized by the cells. Cell uptake of DNA-templated nanostructures was enhanced after encapsulating the nanostructure with layers of polyelectrolytes (PSS and PAH) and targeting ligands. Transmission electron microscope (TEM) images provided evidence that the nanostructures were localized in vesicles in the cytoplasm of the cells. The results from this study suggest that gold, iron oxide, and cobalt iron oxide DNA-templated nanostructures do not induce in vitro toxicity.
ACS Appl Mater Interfaces 2010 May
PMID:In vitro cytotoxic evaluation of metallic and magnetic DNA-templated nanostructures. 2042 63

A versatile and robust adsorbent with both magnetic property and very high adsorption capacity is presented on the basis of functionalization of iron oxide-silica magnetic particles with carboxylic hyperbranched polyglycerol (Fe(3)O(4)/SiO(2)/HPG-COOH). The structure of the resulting product was confirmed by Fourier transform infrared (FTIR) spectra, thermo gravimetric analysis (TGA), zeta-potential, and transmission electron microscopy (TEM). According to the TGA results, the density of the carboxylic groups on the surface of Fe(3)O(4)/SiO(2)/HPG-COOH is calculated to be as high as 3.0 mmol/g, posing a powerful base for adsorbing dyes and drugs. Five kinds of dyes and one representative anticancer drug were chosen to investigate the adsorption capacity of the as-prepared magnetic adsorbent. The adsorbent shows highly efficient adsorption performance for all of the adsorbates especially for the cationic dyes and drug. For example, the saturated adsorption capacity of the Fe(3)O(4)/SiO(2)/HPG-COOH for methyl violet (MV) can reach 0.60 mmol/g, which is much higher than the previous magnetic adsorbents (usually lower than 0.30 mmol/g). 95% of MV and 90% of R6G could be adsorbed within 5 min, and both of the adsorptions reached equilibrium in about 15 min. The adsorption kinetics and isotherm of the adsorbents were investigated in detail and found that the kinetic and equilibrium adsorptions are well-modeled using pseudo-second-order kinetics and Langmuir isotherm model, respectively. In addition, the influences of pH and ionic strength on the adsorption capacity were also examined and found that pH has much greater effect on the adsorption capacity compared with the ionic strength. Regeneration experiments showed that the Fe(3)O(4)/SiO(2)/HPG-COOH can be well-regenerated in ethanol and partially regenerated in 1 M HCl aqueous solution. After regeneration, the magnetic adsorbents can still show high adsorption capacity even for 10 cycles of desorption-adsorption. No obvious decreases of magnetic intensity and aggregation of adsorbents can be observed even after 10 cycles of adsorption-desorption.
ACS Appl Mater Interfaces 2010 May
PMID:Magnetic dendritic materials for highly efficient adsorption of dyes and drugs. 2045 67

Unusual room-temperature weak ferromagnetism alpha-Fe(2)O(3) was prepared by heating the mixture of commercial alpha-Fe(2)O(3) (as raw material) and tartaric acid at a mild temperature of 250 degrees C. This reaction involves a fast heating and cooling process resulting from the self-catalyzed oxidation of tartaric acid. Careful chemical analyses confirmed that no any ferromagnetic impurities, such as Fe, Fe(3)O(4), amorphous iron oxide and gamma-Fe(2)O(3,) were present in the treated sample. The unusual weak ferromagnetism was then attributed to the formation of a large amount of point defects in the treated sample during the peculiar synthetic process. Such a mechanism is supported by the result of annealing, which reduces the amount of point defects and thereby reestablishes the original antiferromagnetism in alpha-Fe(2)O(3).
ACS Appl Mater Interfaces 2010 Jun
PMID:Room-temperature weak ferromagnetism induced by point defects in alpha-Fe2O3. 2048 11


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