A supramolecular assembly strategy towards organic luminescent materials.

Supramolecular organic luminescent materials with different dimensionalities usually exhibit different optical properties as well as their potential applications in various fields. Recent reports showed that non-covalent interactions are useful tools to obtain diverse luminescent materials due to their dynamicity and reversibility, including π-π stacking, host-guest interactions, hydrophobic effects, hydrogen bonding, electrostatic effects and so on. In this review, we summarized recent progress in zero-, one-, two-, three-dimensional and disordered organic luminescent materials using the aforementioned strategies, in order to provide a solution for designing luminescent materials with specific structures and morphologies. The relationship between assembly behavior and luminescent properties is discussed in detail, along with the existing difficulties hindering the development of supramolecular assembly systems and future research directions.

Activating Room-Temperature Phosphorescence of Organic Luminophores via External Heavy-Atom Effect and Rigidity of Ionic Polymer Matrix*.

Pure organic room-temperature phosphorescence (RTP) materials have attracted wide attention for their easy preparation, low toxicity, and applications in various fields like bioimaging and anti-counterfeiting. Developing phosphorescent systems with more universality and less difficulty in synthesis has long been the pursuit of materials scientists. By employing a polymeric quaternary ammonium salt with an ionic bonding matrix and heavy atoms, commercial fluorescent dyes are directly endowed with phosphorescence emission. In a single amorphous polymer, the external heavy-atom effect generates excited triplet states and the rigid polymer matrix stabilizes them. This study put forward a new general strategy to design and develop pure organic RTP materials starting from existing library of organic dyes without complicated chemical synthesis.

Current situation and forecast of environmental risks of a typical lead-zinc sulfide tailings impoundment based on its geochemical characteristics.

The potential environmental implications of a Pb (Lead)-Zn (Zinc) sulfide tailing impoundment were found to be dependent on its geochemical characteristics. One typical lead-zinc sulfide tailing impoundment was studied. Ten boreholes were set with the grid method and 36 tailings were sampled and tested. According to the results of metal content analysis, the tailing samples contained considerably high contents of heavy metals, ranging from 6.99 to 89.0 mg/kg for Cd, 75.3 to 602 mg/kg for Cu, 0.53% to 2.63% for Pb and 0.30% to 2.54% for Zn. Most of the heavy metals in the sample matrix showed a uniform concentration distribution, except Cd. Cd, Pb, Zn, and Mn were associated with each other, and were considered to be the dominant contributors based on hierarchical cluster analysis. XRD, SEM and XPS were employed for evaluation of the tailing weathering characteristics, confirming that the tailings had undergone intensive weathering. The maximum potential acidity of the tailings reached 244 kg H2SO4/ton; furthermore, the bioavailability of heavy metals like Pb, Cd, Cr, Cu, and Zn was 37.8%, 12.9%, 12.2%, 5.95%, and 5.46% respectively. These metals would be potentially released into drainage by the weathering process. Analysis of a gastrointestinal model showed that Pb, Cr, Ni and Cu contained in the tailings were high-risk metals. Thus, control of the heavy metals' migration and their environmental risks should be planned from the perspective of geochemistry.

Leachability characteristic of heavy metals and associated health risk study in typical copper mining-impacted sediments.

A total of 100 samples were collected from the sediments of a typical copper mining area, south China. Leaching concentrations of selected heavy metals (Ni, Cd, Cu, Pb, Zn, Ba, As, and Hg) were measured to evaluate their distribution patterns and associated health risk. Leaching concentrations of Cu (3.58 ±â€¯1.49 mg/L), Pb (1.50 ±â€¯1.06 mg/L), and Zn (4.04 ±â€¯1.68 mg/L) were significantly higher than the other metals in the samples. By evaluating the spatial heterogeneity, it was found that leaching metal concentrations did not decrease with environmental gradients, mostly caused by diverse distribution in pollution sources. The hazard index and carcinogenic risk indices showed significant risks of human exposure. For public safety, priority governance should be given to the main pollutants (Cd, Cu, Pb, Zn, and As) in sediments. In future studies, the integrated data will be urgently required for local stakeholders to conduct environmental monitoring and remediation scenarios.