Suppressing Non-Radiative Relaxation through Single-Atom Metal Modification for Enhanced Fluorescence Efficiency in Molybdenum Disulfide Quantum Dots.

To enhance the fluorescence efficiency of semiconductor nanocrystal quantum dots (QDs), strategies via enhancing photo-absorption and eliminating non-radiative relaxation have been proposed. In this study, we demonstrate that fluorescence efficiency of molybdenum disulfide quantum dots (MoS QDs) can be enhanced by single-atom metal (Au, Ag, Pt, Cu) modification. Four-fold enhancement of the fluorescence emission of MoS QDs is observed with single-atom Au modification.

The atmospheric lead emission, deposition, and environmental inequality driven by interprovincial trade in China.

Lead (Pb) as a hazardous air pollutant has raised widespread concerns due to its adverse and toxic effects on the ecological environment and human health. Here we integrated the multi-regional input-output (MRIO) model and an atmospheric transport model to examine regional environmental inequality (REI) index induced by Pb emission transfers, and to evaluate the impacts of interprovincial trade on regional atmospheric Pb concentrations and dry deposition fluxes in China in 2012. In 2012, approximately 57.

Single-Molecule MicroRNA Electrochemiluminescence Detection Using Cyclometalated Dinuclear Ir(III) Complex with Synergistic Effect.

The realization of electrochemiluminescence (ECL) detection at the single-molecule level is a longstanding goal of ECL assay that requires a novel ECL probe with significantly enhanced luminescence. Here, the synergistic effect of electrochemiluminescence (ECL) is observed unprecedentedly in a new cyclometalated dinuclear Ir(III) complex [Ir(dfppy)(imiphenH)]PF (·PF, PF = hexafluorophosphate) in which two {Ir(dfppy)} units are bridged by an imiphenH ligand. The ECL intensity from complex ·PF is 4.

Axial ligands tailoring the ORR activity of cobalt porphyrin.

In an effort to provide visualization and understanding to the electronic "push effect" of axial ligands on the catalytic activity of cobalt macrocyclic molecules, we design a simple model system involving an [5,10,15,20-tetrakis(4-methoxyphenyl)porphyrin]cobalt(II) (TMMPCo) monolayer axially-coordinated on thiol ligand modified Au electrode and explore the activity of the axial-ligand coordinated TMPPCo toward oxygen reduction reaction (ORR) in acidic medium. Three different ligands, with a decreasing order of coordinating ability as: 4-mercaptopyridine (MPy) > 4-aminothiolphenol (APT) > 4-mercaptobenzonitrile (MBN) are used and a maximum difference in ORR onset potential of 80 mV is observed between the MPy (highest onset potential) and MBN systems (lowest onset potential). The ORR activity of TMPPCo increases with the increase in binding strength of the axial ligand.

Three novel isomeric zinc metal-organic frameworks from a tetracarboxylate linker.

Three porous supramolecular isomers (IZE-1, IZE-2, and IZE-3) with the same framework component [Zn(2)(EBTC)(H(2)O)(2)] (EBTC = 1,1'-ethynebenzene-3,3',5,5'-tetracarboxylate) were successfully constructed by finely tuning the reaction condition. Although both IZE-1 and IZE-2 are constructed from the linear EBTC subunits and one kind of regular [Zn(2)(CO(2))(4)] paddlewheels, their frameworks exhibit two different (3,4)-c net of fof (sqc1575) and sqc1572, respectively, resulting in cavities with different size and shape. However, as for isomer IZE-3, the EBTC ligands are bent and one-half of the [Zn(2)(CO(2))(4)] paddlewheels are distorted, leading to a novel (3,4,4)-c hyx net with point symbol (6.

[Structures of leucogen and its related substances in solution state].

Aim: To study the four diastereomers of leucogen and structure of the related substances.

Methods: LC-DAD, LC-MS/MS and LC- 1H NMR were used. LC was carried out with a Phenomnex Luna C18 (250 mm x 4.