Adaptive organic nanoparticles of a teflon-coated iron (III) porphyrin catalytically activate dioxygen for cyclohexene oxidation.

Self-organized organic nanoparticles (ONP) are adaptive to the environmental reaction conditions. ONP of fluorous alkyl iron(III) porphyrin catalytically oxidize cyclohexene to the allylic oxidation products. In contrast, the solvated metalloporphyrin yields both allylic oxidation and epoxidation products. The ONP system facilitates a greener reaction because about 89% reaction medium is water, molecular oxygen is used in place of synthetic oxidants, and the ambient reaction conditions used require less energy. The enhanced catalytic activity of these ONP is unexpected because the metalloporphyrins in the nanoaggregates are in the close proximity and the TON should diminish by self-oxidative degradation. The fluorous alkyl chain stabilizes the ONP toward self-oxidative degradation.

Pistachio shells as remediating agents for uranium in contaminated industrial seawater.

Waterways have histories of being contaminated by heavy and/or radioactive metals produced by industrial processes. Natural radioisotopes of uranium (238U, 235U and 234U), long-lived radiometals, are widespread in the environment as a result of both naturally occurring processes and anthropogenic processes. Uranium is considered a major threat to humans. Previous research has focused on using inorganic materials (e.g. ion-exchangers, extractants, nanoporous sorbents) to remove such metal. However, there has been a rise in using biodegradable, recyclable, and organic biological wastes to remove heavy toxic metals from aqueous solutions. The purpose of this study is to identify pistachio shells as good candidates for the removal of uranyl from aqueous solutions. The influences of pH, contact time, temperature, and initial uranyl concentration on uranyl uptake were investigated. The influence of pH was observed to be variable, with relatively high uptake occurring at pH 4 and at slightly alkaline pH values. Uptake increased as a function of contact time, temperature, and initial uranyl concentration. The mechanism followed pseudo-second-order and intraparticle kinetics models, and the shell was demonstrated to be a Freundlich isotherm. The shells were successfully demonstrated to be viable adsorbents for uranium in seawater samples, with obtained trends similar to those achieved in the batch studies.

Self-assembly of Au Nanoparticle-containing Peptide Nano-rings on Surfaces.

The peptide nano-rings containing Au nanoparticles inside their cavities were self-assembled on dithiol SAMs patterned as an array by AFM-based nanolithography. The peptide nano-rings were aligned as a line on these SAMs, and Au formed lines with the spacing between these nanoparticles as the peptide nano-rings functioned as spacers. This type of array fabrication will provide improved tunability in their optical properties of resulting nanoparticle-assembled arrays. In addition, optimization of the inter-particle distance of nanoparticles in the array with various spacers may allow one to design new types of photonic crystals with desired optical properties.

Fabrication of Size-Tunable Metallic Nanoparticles Using Plasmid DNA as a Biomolecular Reactor.

Plasmid DNA can be used as a template to yield gold, palladium, silver, and chromium nanoparticles of different sizes based on variations in incubation time at 70 °C with gold phosphine complexes, with the acetates of silver or palladium, or chromium acetylacetonate. The employment of mild synthetic conditions, minimal procedural steps, and aqueous solvents makes this method environmentally greener and ensures general feasibility. The use of plasmids exploits the capabilities of the biotechnology industry as a source of nanoreactor materials.

Fabrication of metal nanoparticles using toroidal plasmid DNA as a sacrificial mold.

A new method for synthesizing gold, nickel, and cobalt metal nanoparticles at room temperature from metal salts employing plasmid DNA in a toroidal topology as a sacrificial mold is presented. The diameter of the toroidal DNA drives the formation and size of the nanoparticle, and UV light initiates the oxidation of the DNA and concomitant reduction of the DNA bound metal ions. The nanoparticles were characterized by atomic force microscopy (AFM), transmission electron microscopy (TEM), and electron diffraction (ED).

Doughnut-shaped peptide nano-assemblies and their applications as nanoreactors.

Doughnut-shaped nanoreactors, peptide nano-doughnuts, were self-assembled from peptides and organic Au salts. We demonstrated that monodisperse Au nanocrystals were synthesized inside the cavities of peptide nano-doughnuts by the reduction of Au ions and the size of the Au nanocrystal was controlled by the cavity dimension. The Au nanocrystals inside the nano-doughnuts were extracted by destroying the nano-doughnuts via long UV irradiation (>10 h). These features may allow the peptide nano-doughnuts to be applied in the fields of nanomaterial syntheses, controlled release systems, and drug delivery.