Generation, detection and characterization of optical minimum shift keying data format

This paper presents the detailed principle on the generation and detection of optical minimum shift keying (MSK) format for high-speed and high spectral efficiency WDM systems. 10.7 Gb/s optical MSK data is successfully generated by experiment using the proposed scheme. The results show that optical MSK signal exhibits very compact optical spectrum, which is promising for high spectral efficiency WDM applications. Simulation results on dispersion and nonlinear tolerance comparison confirm that MSK signal has better dispersion tolerance and nonlinear tolerance compared with 50% duty cycle return-to-zero differential phase shift keying (RZ-DPSK) and 50% duty cycle RZ on-off-keying (RZ-OOK) formats.     

单摆周期的数值计算

本文从理论上分析了单摆周期随角振幅变化的规律，并给出了数值计算结果     

Acid‐treated g‐C3N4‐Cu2O composite catalyst with enhanced photocatalytic activity under visible‐light irradiation

Acid‐treated g‐C₃N₄‐Cu₂O was prepared by hydrothermal reduction followed by high temperature calcination and acid exfoliation. The structures and properties of as‐synthesized samples were characterized using a range of techniques, such as X‐ray photoelectron spectroscopy, scanning electron microscopy, Photoluminescence Spectroscopy and the Brunauer–Emmett–Teller (BET) theory. The photocatalytic activity was evaluated by measuring the photodegradation of methyl orange under visible‐light irradiation. Based on the results of TEM, XPS, EPR and other techniques, it was verified that a heterojunction was formed. The acid treatment process can increase the specific surface area to form abundant heterojunction interfaces as channels for photo‐generated carrier separation, thereby enhancing its light utilization and quantum efficiency. Results indicate that acid‐treated g‐C₃N₄‐Cu₂O possesses a large specific surface area, which provides plentiful activated sites for heterojunctions to form; in addition, it showed a high visible light effect and the minimum charge‐transfer resistance. Furthermore, the g‐C₃N₄‐Cu₂O material exhibits high levels of effectiveness and stability. Electron paramagnetic resonance and a series of radical trapping experiments demonstrate that the holes and ?O₂^? could be the main active species in methyl orange photodegradation. This work could provide new insights into the fabrication of composite materials as high‐performance photocatalysts, and facilitate their application in addressing environmental protection issues.     

Direct synthesis, crystal structure and thermal analyses of 2-nitroterephthalate and carbohydrazide bridged staircase-like 3D packing grids of lead(II)

X-ray single crystal diffraction demonstrates that in {[Pb₂(HNTP)₂(NTP)(CHZ)(H₂O)₂] · 2.5H₂O} _n (polymer, NTP = nitroterephthalate, CHZ = carbohydrazide), there are two kinds of Pb centers. By means of the bridging ligands–two water, two CHZ and two NTP molecules, four Pb centers (two Pb1 and two Pb2) are joined together to form the rectangular grid, and by the intense static electric interactions among the two O atoms of nitro groups in NTP, the extending two-dimensional grids are linked together to form the three-dimensional frameworks. Thermal analyses DSC and TG-DTG have been performed on the polymer to study its thermal decomposition mechanism and thermal kinetic properties. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Synthesis of hyperbranched degradable polymers by atom transfer radical (Co)polymerization of inimers with ester or disulfide groups

Degradable hyperbranched polymers with multiple alkyl halide chain ends were synthesized by the atom transfer radical polymerization of inimers containing ester (2‐(2′‐bromopropionyloxy)ethyl acrylate) or disulfide (2‐(2′‐bromoisobutyryloxy)ethyl 2′′‐methacryloyloxyethyl disulfide) groups. Both the homo‐ and copolymerizations (with styrene in the former case and methyl methacrylate in the latter) were studied. The hyperbranched polymers derived from the ester‐type inimer were hydrolytically degradable under basic conditions, whereas those derived from the disulfide‐containing inimer could be efficiently degraded in the presence of reducing agents such as tributylphosphine. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2009     

锌离子对聚乳酸结晶和热性能的影响

本文发现了Zn(II)离子掺杂可以加快聚乳酸的结晶过程. 测试了三种Zn(II)盐(ZnCl₂、ZnSt和ZnOAc),并与其它离子Mg(II)和Ca(II)进行对照. FT-IR以及变温拉曼光谱分析发现,经Zn(II)离子掺杂后,聚乳酸的结晶度和结晶速率均增加,差示扫描量热技术以及X射线衍射分析也进一步证实. 差示扫描量热技术测定PLA/ZnSt-0.4 wt%材料的结晶率达到22.46%,PLA/ZnOAc-0.4 wt%材料的结晶率达到24.83%.     

Fluorometric determination of the activity and inhibition of terminal deoxynucleotidyl transferase via in-situ formation of copper nanoclusters using enzymatically generated DNA as template

The authors report on a simple strategy for sensitive determination of the activity of terminal deoxynucleotidyl transferase (TdT) using copper nanoclusters (CuNCs) as fluorescent probes. TdT-polymerized long chain AT-rich DNA serves as a template for the synthesis of the CuNCs, and TdT activity is detected fluorometrically at excitation/emission wavelengths of 340/570 nm. The protocol relies on the target-triggered formation of dsDNA polymers and in-situ formation of CuNCs. The calibration plot is linear in the 0.7 to 14 U L^?1 activity range, with a 60 mU L^?1 detection limit (at a signal-to-noise ratio of 3). The protocol was applied to determine TdT activity in acute lymphatic leukemia cells. This approach is selective, simple, convenient and cost-efficient because a complex DNA sequence is not required. In our perception, the method provides a viable new platform for monitoring the activity and inhibition of TdT.

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Graphical abstract Based on the target-triggered formation of dsDNA polymers and in-situ formation of CuNCs with strong fluorescence, a turn-on fluorescence assay for TdT activity is presented.

     

Pharmacophore Modeling and Virtual Screening of Novel Inhibitors for c-Kit Kinase

The stem cell factor receptor (c‐Kit) has been known to play critical roles in regulating numerous aspects of cellular behavior including cell growth, differentiation, migration and metabolism. In this investigation, a three‐dimensional pharmacophore model of c‐Kit inhibitors has been established by using the HypoGen algorithms implemented in the catalyst software package. The best quantitative pharmacophore model, hypothesis 1, which has the highest correlation coefficient (0.989), consists of one hydrogen bond acceptor, two hydrogen bond donors and one hydrophobic feature. To our knowledge, this is the first report on the pharmacophore modeling study of c‐Kit inhibitors. The best hypothesis, hypothesis 1, was used to screen molecular structural databases, including Specs and China Natural Products Database for potential lead compounds. The hit compounds were subsequently subjected to filtering by Lipinski's rules and docking study to refine the retrieved hits and as a result to reduce the rate of false positive. Finally 28 compounds were purchased or synthesized for further in vitro assay against several human tumour cell lines including A549, MCF‐7, HepG2 and PC‐3, in which c‐Kit is overexpressed. Two compounds show very low micromolar inhibition potency against the PC‐3 and HepG2 cell lines respectively. And they were selected for further modification and testing.