One-Step Synthesis of Peptide-Gold Nanoclusters with Tunable Fluorescence and Enhanced Gene Delivery Efficiency.

In this study, peptide-gold nanoclusters with tunable fluorescence were prepared by a simple "one-pot" method, which were used for gene localization and delivery in vivo to achieve efficient intracellular colocalization, uptake, and transfection. The efficiency of pDNA transfection was up to 70.6%, and there was no obvious cytotoxicity. This study proves that the simple-composition and bio-friendly peptide-gold nanoclusters are promising gene delivery carriers and can provide a powerful theoretical and experimental basis for the application of peptide-metal nanocomplexes in gene delivery and other biomedicine fields.

Pickering Emulsions Stabilized by Lignin/Chitosan Nanoparticles for Biphasic Enzyme Catalysis.

In this study, we construct a green and high-performance platform using Pickering emulsions for biphasic catalysis. The oil-in-water Pickering emulsions stabilized by the lignin/chitosan nanoparticles (Lig/Chi NPs) have great stability and alkali resistance, showing pH-responsive reversible emulsification and demulsification which can be recycled at least three times. The Pickering emulsion also has fluorescence and wide availability to different oil-to-water volume ratios, types of oil, storage times, temperatures, and ion concentrations. When this system is applied to the lipase-catalyzed reaction for the hydrolysis of p-nitrophenol palmitate, it will provide stable and large oil-water reaction interface areas, and the negatively charged lipase will enrich at the emulsion interface by electrostatic adsorption of the positively charged Lig/Chi NPs to achieve immobilization (lipase-Lig/Chi NPs). The reaction conversion rate can reach nearly 100% in 30 min, which is nearly three times higher than that of the conventional two-phase system. Moreover, the lipases in Pickering emulsion stabilized by Lig/Chi NPs exhibit great recyclability because of the protection of Lig/Chi NPs.

Circularly Polarized Luminescent Chiral Photonic Films Based on the Coassembly of Cellulose Nanocrystals and Gold Nanoclusters.

In this work, we studied the formation and properties of composite films coassembled by cellulose nanocrystals (CNCs) and bovine serum albumin-stabilized gold nanoclusters (BSA-AuNCs). The influences of the BSA-AuNC concentration on the structure and optical properties of CNC-based composite films were further studied. It was found that the composite film retained the chiral nematic structure and optical activity. The self-assembled CNC and BSA-AuNC helical superstructures can produce strong, left-handed, circularly polarized luminescence with dissymmetry factors up to 0.287. Meanwhile, the third component, polyethylene glycol, was introduced without affecting the structural color and fluorescence characteristics of the composite film to enhance the flexibility of the film. The simplicity of the film preparation, the abundance of CNCs, and the flexibility and stability of the composite films pave the way for the production of functional materials with integrated functions.

Bis(2,2'-bipyridine-κN,N')(4-methyl-benzoato-κO,O')copper(II) iodide hemihydrate.

The title compound, [Cu(C(8)H(7)O(2))(C(10)H(8)N(2))(2)]I·0.5H(2)O, was obtained by the hydro-thermal reaction of copper(I) iodide, 4-methyl-benzoic acid and 2,2'-bipyridine. The initial reactant of Cu(I) was oxidized to Cu(II). The asymmetric unit contains two independent complex mol-ecules, two I(-) ions and one water molecule. Each Cu(II) atom is coordinated by two O atoms from a 4-methyl-benzoate ligand and four N atoms from two 2,2'-bipyridine ligands, displaying a distorted octa-hedral geometry. The structure involves O-H⋯I hydrogen bonds between the water mol-ecule and iodide ions and π-π stacking inter-actions between the benzene and pyridyl rings [centroid-centroid distance = 3.79 (1) Å] and between the pyridyl rings [centroid-centroid distance = 3.87 (1) Å].