Recently, the emergence of conductive metal-organic frameworks (MOFs) has given great prospects for their applications as active materials in electronic devices. In this work, a high-quality, free-standing conductive MOF membrane was prepared by an air-liquid interfacial growth method. Accordingly, field-effect transistors (FETs) possessing a crystalline microporous MOF channel layer were successfully fabricated for the first time. The porous FETs exhibited p-type behavior, distinguishable on/off ratios, and excellent field-effect hole mobilities as high as 48.6 cm V s, which is even comparable to the highest value reported for solution-processed organic or inorganic FETs.

In order to reveal the biocompatibility of Fe(3)O(4) nanoparticles and bipolar surfactant tetramethylammonium 11-aminoundecanoate cytotoxicity tests were performed as a function of concentration from low (0.1 microg ml(-1)) to higher concentration (100 microg ml(-1)) using various human glia, human breast cancer and normal cell lines. Cytotoxicity tests for human glia (D54MG, G9T, SF126, U87, U251, U373), human breast cancer (MB157, SKBR3, T47D) and normal (H184B5F5/M10, WI-38, SVGp12) cell lines exhibited almost nontoxicity and reveal biocompatibility of Fe(3)O(4) nanoparticles in the concentration range of 0.1-10 microg ml(-1), while accountable cytotoxicity can be seen at 100 microg ml(-1). The results of our studies suggest that Fe(3)O(4) nanoparticles coated with bipolar surfactant tetramethylammonium 11-aminoundecanoate are biocompatible and promising for bio-applications such as drug delivery, magnetic resonance imaging and magnetic hyperthermia.

Lithium–sulfur (Li–S) batteries are appealing candidates for next‐generation high‐energy rechargeable batteries, but practical applications are still limited by poor cyclic life, which is caused by severe polysulfide shuttling in high‐sulfur‐loading batteries. Herein, a facile route is presented to fabricate high‐performance Li–S batteries using a crystalline microporous membrane, which is prepared using a conductive metal–organic framework (MOF) material. With ordered microporous structure, large specific surface area, good sulphiphilicity, and excellent conductivity, the MOF membrane is grown in situ on the commercial separator and is an ideal light‐weight barrier (0.066 mg cm−2) for suppressing the polysulfide shuttling, which can significantly promote the capacities, rate capabilities, and cycling stabilities of Li–S batteries. Taking the advantage of this functional separator, the high‐sulfur‐loading Li–S battery (8.0 mg cm−2 and 70 wt% of sulfur in cathode) delivers a high area capacity of 7.24 mAh cm−2 after 200 cycles, thus providing a promising path toward advanced Li–S batteries.

No abstract

No abstract

Despite significant progress achieved in the preparation of chiral nanoparticles, the enantioseparation of racemates still presents a big challenge in nanomaterial research. Herein, we report the synthesis and structural characterization of racemic anisotropic nanocluster Ag 30 (C 2 B 10 H 9 S 3 ) 8 Dppm 6 ( Ag 30 - rac ), which is protected by mixed carboranetrithiolate and phosphine ligands. Spontaneous self-resolution of the racemates was realized through conglomerate crystallization in dimethylacetamide (DMAc). The homochiral nanoclusters in the racemic conglomerates adopt enantiomeric helical self-assemblies ( R / L - Ag 30 ). Diverse noncovalent interactions as the driving force in directing superstructure packing were elucidated in detail. Furthermore, the nanoclusters show red luminescence in both solid and solution states, and the racemic conglomerates display a mirror-image CPL response. This work provides atom-precise helical nanoparticle superstructures that facilitate an in-depth understanding of the helical-assembly mechanism.

A successful polymeric gene delivery vector is denoted by both transfection efficiency and biocompatibility. However, the existing vectors with combined high efficacy and minimal toxicity still fall short. The most widely used polyethylene imine (PEI), polyamidoamine (PAMAM) and poly(dimethylaminoethyl methacrylate) (PDMAEMA) suffer from the correlation: either too toxic or little effective. Here, we demonstrate that with highly branched poly(β-amino esters) (HPAEs), a type of recently developed gene delivery vector, the high gene transfection efficiency and low cytotoxicity can be achieved simultaneously at high molecular weight (MW). The interactions of HPAE/DNA polyplexes with cell membrane account for the favorable correlation between molecular weight and biocompatibility. In addition to the effect of molecular weight, the molecular configuration of linear and branched segments in HPAEs is also pivotal to endow high transfection efficiency and low cytotoxicity. These findings provide renewed perspective for the further development of clinically viable gene delivery vectors.

A new azodioxy-linked porphyrin-based semiconductive covalent organic framework with I 2 doping-enhanced photoconductivity A homogeneous solution phase reaction at ambient condition is employed to prepare a porphyrin based Covalent Organic Framework (COF). The electrical conductivity of the newly reported COF increases more than three orders on iodine doping and it shows doping induced photo-current generation.