Effect of the ligand shell composition on the dispersibility and transport of gold nanocrystals in near-critical solvents.

The development of more efficient and environmentally benign methods for the synthesis and manipulation of nanomaterials has been a major focus of research among the scientific community. Supercritical (ScFs) and near-critical fluids (NcFs) offer numerous advantages over conventional solvents for these purposes. Among them, ScFs and NcFs offer dramatic reductions in the volume of organic waste typically generated during advanced material processes with the feasibility of changing a number of physicochemical properties by discrete variations in solvent pressure or temperature.

Advancements toward the greener processing of engineered nanomaterials--effect of core size on the dispersibility and transport of gold nanocrystals in near-critical solvents.

The ability to process and purify engineered nanomaterials using near critical or supercritical fluids (NcFs or ScFs) has enormous potential for the application at various stages of the development of green nanomaterials. The dispersibility of octanethiol-stabilized gold nanocrystals of different core sizes is explored, which were chosen to serve as model nanomaterials of general interest in compressed ethane and propane over a wide range of fluid conditions. Both solvents have enormous potential for the environmentally benign processing and transport of engineered nanomaterials due to their nominal toxicity and high degree of tunability and processability that can essentially eliminate solvent waste.

A solution NMR investigation into the early events of amelogenin nanosphere self-assembly initiated with sodium chloride or calcium chloride.

Using solution-state NMR spectroscopy, new insights into the early events governing amelogenin supramolecular self-assembly have been identified using sodium chloride and calcium chloride to trigger the association. Two-dimensional 1H-15N HSQC spectra were recorded for 15N- and 13C-labeled murine amelogenin as a function of increasing NaCl and CaCl2 concentration beginning with solution conditions of 2% acetic acid at pH 3.0, where amelogenin was monomeric.

1H, 13C, and 15N resonance assignments of murine amelogenin, an enamel biomineralization protein.

Amelogenin is the predominant matrix protein in developing dental enamel. Making extensive use of residue specific 15N-labeled amino acids samples, the majority of the main and side chain resonances for murine amelogenin were assigned in 2% aqueous acetic acid at pH 3.0.