Translocation and distribution of mercury in biomasses from subtropical forest ecosystems:evidence from stable mercury isotopes

To understand its source,distribution,storage,and translocation in the subtropical forest ecosystems,mercury(Hg)concentrations and stable isotopes in forest biomass tissues(foliage,branch,bark,and trunk)were investigated at Ailao Mountain National Nature Reserve,Southwest China.The total Hg(THg)concentrations in the samples show the following trend:mature foliage(57±19 ng g-1)>bark(11±4.0 ng g-1)>branch(5.4±2.5 ng g-1)>trunk(1.6±0.7 ng g-1).Using the measured THg concentrations and the quantity of respective biomasses,the Hg pools in the forest are:wood(60±26μg m-2)>bark(51±18μg m-2)>foliage(41±11μg m-2)>branch(26±8.3μg m-2).The tree biomasses displayed negativeδ202Hg(-1.83‰to-3.84‰)andΔ199Hg(-0.18‰to-0.62‰).The observedΔ200Hg(-0.08‰to 0.04‰)is not significantly from zero.AΔ199Hg/Δ201Hg ratio of 1.05 was found in tree biomasses,suggesting that mercury has undergone Hg(Ⅱ)photoreduction processes.A Hg-isotope based binary mixing model suggests that Hg in the tree biomasses mainly originated from foliage uptake of atmospheric Hg0,constituting 67%,80%,and 77%of Hg in wood,branch,and bark,respectively.Our study sheds new light on the transportation and sources of Hg in the subtropical forest ecosystems.

A Red-Emissive Sextuple Hydrogen-Bonding Self-Assembly Molecular Duplex Bearing Perylene Diimide Fluorophores for Warm-White Organic Light-Emitting Diode Application

A novel sextuple hydrogen-bonding （HB） self-assembly molecular duplex bearing red-emitting perylene diimide （PDI） fluorophores, namely PDIHB, was synthesized, and its molecular structure was confirmed by IH NMR, 13C NMR, TOF-MS and 2D NMR. Compared with the small molecular reference compound PDI, PDIItB shows one time enhanced fluorescence efficiency in solid state （4.1% vs. 2.1%）. More importantly, the presence of bulky HB oli- goamide strands in PDIHB could trigger effective spatial separation between guest and host fluorophores in thin solid film state, hence inefficient energy transfer occurs between the blue-emitting host 2TPhNII/B and red guest PDIHB in the 2 wt% guest/host blending film. As a result, a solution-processed organic light-emitting diode （OLED） with quite simple device structure of ITO/PEDOT：PSS （40 nm）/PVK （40 nm）/PDIHB （2 wt%）： 2TPhNII-IB （50 nm）/LiF （0.8 nm）/A1 （100 nm） could emit bias-independent warm-white electroluminescence with stable Commission Intemationale de L＇Eclairage coordinates of （0.42, 0.33）, and the maximum brightness and current efficiency of this device are 260 cdom-2 and 0.49 cd·A-1, respectively. All these results indicated that HB self-assembly supramolecular fluorophores could act as prospective materials for white OLED application.

Super-resolution imaging and real-time tracking lysosome in living cells by a fluorescent probe

Lysosomes function as important organelles within cells and their movement associates with diverse biological events, hence the real-time tracking of lysosomal movement is of great significance. However, since most ly so some fluorescent probes suffer from relatively unsatisfactory photo stability,tracking lysosomal movement in real-time remains challenging. Here,we report that a naphthalimide-based fluorescent compound,namely NIMS,is a quite promising probe for ly so some imaging. The visualizing mechanism lies in the selective accumulation of NIMS in lysosomes via a protonation reaction, followed by the fluorescence enhancement due to the interactions of NIMS with proteins. Owing to its high selectivity and good photo stability, NIMS was successfully applied to capture super-resolution fluorescence images of lysosomes. More importantly, real-time tracking of ly so some movement in a single living cell by NIMS was realized with a confocal laser scanning microscope. Surprisingly,even in normal culture conditions, around 2/3 of the captured lysosomes were observed to move within 5 min, indicative of the highly dynamic features of lysosomes. Thus, this probe may facilitate the understanding of the ly so some dynamics in physiologicalor pathological conditions.

A Novel Ratiometric Oxygen Sensor Based On a Sextuple Hydrogen-Bonding Self-Assembly Molecular Heterodimer

A novel sextuple hydrogen-bonding （HB） self-assembly molecular heterodimer bearing an iridium complex as the indicator dye and two carbazoles as the reference dye, namely 6HB-Irbt-Cz, was synthesized, and its molecular structure was confirmed by ^1H NMR, ^13CNMR, TOF-MS and 2D NMR. Because of the inefficient energy transfer process between the carbazole and iridium complex units, 6HB-Irbt-Cz exhibits distinct fluorescence/ phosphorescence dual emission in neat film state. More importantly, the neat film sample of 6HB-Irbt-Cz could display linear ratiometric optical response toward oxygen in the full oxygen concentration range from 0 to 100 vol%, together with good stability, reversibility and rapid response-recovery times. Note that this represents the first discovery of neat-film-based oxygen sensor capable of showing strictly linear ratiometric Stem-Volmer behavior in the oxygen concentration of 0- 100 vol%.

Tetraphenylethylene-conjugated polycation covered iron oxide nanoparticles for magnetic resonance/optical dual-mode imaging

Magnetic resonance(MR)/optical dual-mode imaging with high sensitivity and high tissue resolution have attracted many attentions in biomedical applications.To avert aggregation-caused quenching of conventional fluorescence chromophores,an aggregation-induced emission molecule tetraphenylethylene(TPE)-conjugated amphiphilic polyethylenimine(PEI)covered superparamagnetic iron oxide(Alkyl-PEI-LAC-TPE/SPIO nanocomposites)was prepared as an MR/optical dual-mode probe.Alkyl-PEI-LAC-TPE/SPIO nanocomposites exhibited good fluorescence property and presented higher T2 relaxivity(352 Fe mM1s1)than a commercial contrast agent Feridex(120 Fe mM1s1)at 1.5 T.The alkylation degree of Alkyl-PEI-LAC-TPE effects the restriction of intramolecular rotation process of TPE.Reducing alkane chain grafting ratio aggravated the stack of TPE,increasing the fluorescence lifetime of Alkyl-PEI-LAC-TPE/SPIO nanocomposites.Alkyl-PEI-LAC-TPE/SPIO nanocomposites can effectively labelled HeLa cells and resulted in high fluorescence intensity and excellent MR imaging sensitivity.As an MR/optical imaging probe,Alkyl-PEI-LAC-TPE/SPIO nanocomposites may be used in biomedical imaging for certain applications.