A Conjugated Polymer Containing Arylazopyrazole Units in the Side Chains for Field‐Effect Transistors Optically Tunable by Near Infra‐Red Light

Optically tunable field‐effect transistors (FETs) with near infra‐red (NIR) light show promising applications in various areas. Now, arylazopyrazole groups are incorporated in the side chains of a semiconducting donor–acceptor (D‐A) polymer. The cis–trans interconversion of the arylazopyrazole can be controlled by 980 nm and 808 nm NIR light irradiation, by utilizing NaYF₄:Yb,Tm upconversion nanoparticles and the photothermal effect of conjugated D‐A polymers, respectively. This reversible transformation affects the interchain packing of the polymer thin film, which in turn reversibly tunes the semiconducting properties of the FETs by the successive 980 nm and 808 nm light irradiation. The resultant FETs display fast response to NIR light, good resistance to photofatigue, and stability in storage for up to 120 days. These unique features will be useful in future memory and bioelectronic wearable devices.     

Synthesis,Characterizations, Magnetism and Thermal Degradation of a 2‐Fold Interpenetrated 3D Cobalt‐Organic Framework

A new coordination polymer, [Co₂(L)₂(4,4′‐bipy)]_n·3nH₂O ( 1 ) based on 5‐(3‐methyl‐5‐phenyl‐4H‐1,2,4‐triazol‐4‐yl)isophthalic acid (H₂ L ) and 4,4′‐bipyridine (4,4′‐bipy) has been hydrothermally synthesized and characterized by single‐crystal X‐ray diffraction, XRPD, IR, and elemental analysis. Temperature‐dependent magnetic susceptibility and thermal degradation for 1 were also studied. The asymmetric unit of compound 1 consists of two crystallographically independent Co(II) ion, two L ^2? ligand, one 4,4′‐bipy ligand, and three lattice water molecules. The 2D triangle networks were linked by the bridging 4,4′‐bipy ligand to give rise to a 2‐fold interpenetrated 3D architecture. The simplest cyclic motif of the 2D networks is a triangle ring consisting of three Co(II) cations and three L ^2? ligands. So we can define Co(II) ions as 4‐connected nodes and the L ^2? ligands as 3‐connected nodes. Thus, the 3D structure can be described as a 2‐fold parallel interpenetrated ins InS 3,4‐conn topology.     

Solventless Formation of G‐Quartet Complexes Based on Alkali and Alkaline Earth Salts on Au(111)

Template cations have been extensively employed in the formation, stabilization and regulation of structural polymorphism of G‐quadruplex structures in vitro. However, the direct addition of salts onto solid surfaces, especially under ultra‐high‐vacuum (UHV) conditions, to explore the feasibility and universality of the formation of G‐quartet complexes in a solventless environment has not been reported. By combining UHV‐STM imaging and DFT calculations, we have shown that three different G‐quartet‐M (M: Na/K/Ca) complexes can be obtained on Au(111) using alkali and alkaline earth salts as reactants. We have also identified the driving forces (intra‐quartet hydrogen bonding and electrostatic ionic bonding) for the formation of these complexes and quantified the interactions involved. Our results demonstrate a novel route to fabricate G‐quartet‐related complexes on solid surfaces, providing an alternative feasible way to bring metal elements to surfaces for constructing metal–organic systems.     

新乐工业新区土壤中多种元素的测定

采用湿法消解对不同厂区的土壤进行前处理,应用电感耦合等离子体原子发射光谱法(ICP-OES)测定土壤中的金属元素含量,使用原子荧光光谱法AFS测定砷的含量,测定的相对标准偏差为0.8%～3.0%,回收率为89.0%～105.5%。实验表明,方法简单快速、准确,较高的灵敏度和较低的检出限,均能满足土壤中多元素分析的要求。     

Distributed finite-time coordinated tracking control for multiple Euler–Lagrange systems with input nonlinearity

Nonlinear Dynamics - In this paper, distributed finite-time coordinated tracking control for multiple Euler–Lagrange systems with input nonlinearity is investigated by using backstepping...     

2013年“菲特”台风暴雨数值模拟中微物理方案的对比试验

利用TRMM（热带测雨雷达）搭载的TMI（微波成像仪）反演廓线资料,分析“菲特”台风登陆前、后云团内部水凝物的分布种类,依此选择WRF区域中尺度模式下符合条件的6个云微物理过程参数化方案（Lin,WSM6,Godgce,WDM6,Morrison以及Thompson方案）,模拟2013年10月6~8日的台风过程.从降水落区、强度,水凝物及风场垂直分布,台风路径及强度等方面对预报性能进行对比,结果表明,选用的6个云微物理方案都较好地模拟了浙江暴雨的范围和强度.结合Ts评分,降水量级越大,模拟效果对云微物理方案选择越敏感,其中,Lin方案效果最佳,尤其对极端降水的模拟,其次为WSM6、WDM6及Thompson方案,Morrison和Godgce方案相对较差.结合水凝物平均值廓线分布发现,除WDM6方案外,其他方案对暖雨过程的模拟基本一致,而对冰相过程的模拟6个方案差别较大;同时,各方案对风分量的模拟结果较水凝物廓线差别小,说明对于动力因素模拟不敏感.另外,6个方案对于台风强度的模拟整体偏弱,相较之下,Lin方案较好地模拟了强度变化趋势.     

MULTIAXIAL BEHAVIOR OF NANOPOROUS SINGLE CRYSTAL COPPER： A MOLECULAR DYNAMICS STUDY

The stress-strain behavior and copper are studied by the molecular dynamics incipient yield surface of nanoporous single crystal （MD） method. The problem is modeled by a periodic unit cell subject to multi-axial loading. The loading induced defect evolution is explored. The incipient yield surfaces are found to be tension-compression asymmetric. For a given void volume fraction, apparent size effects in the yield surface are predicted： the smaller behaves stronger. The evolution pattern of defects （i.e., dislocation and stacking faults） is insensitive to the model size and void volume fraction. However, it is loading path dependent. Squared prismatic dislocation loops dominate the incipient yielding under hydrostatic tension while stacking-faults are the primary defects for hydrostatic compression and uniaxial tension/compression.     

Thermodynamics analysis of indium iodide polycrystal synthesis

According to the thermodynamics analysis, the molar enthalpy change, the molar entropy increase, the Gibbs free energy change and the balance constant of indium iodide polycrystal synthesis reaction were calculated in order to evaluate the feasibility of reaction temperature on 653 K. After the temperature 653 K was applied in the synthesis experiment, indium iodide polycrystal was successfully obtained by the two‐zone vapor transporting method. The result of X‐ray diffraction analysis indicates the temperature 653K can be used for indium iodide polycrystal synthesis.     

New ferrocenyl derivative with controllable aggregation-induced emission (AIE) characteristics

A novel molecular switch, 7-(N,N-diethylamino)-2-oxo-2H-chromen-4-yl ferrocene carboxylate (FCC), was synthesized and fully characterized by ¹H NMR, ¹³C NMR, and HRMS. Taking advantage of the properties of ferrocene as an electron donor active unit and the coumarin as a fluorescent unit, the dyad FCC shows a fast and reversible redox-switchable fluorescence emission. In sharp contrast to most photoluminescent chromophores, FCC has a unique enhanced emission through aggregation. The change of electrochemical signals (CV and DPV) indicated that the ferrocene (F_c) unit of FCC could form inclusion complex with Me-β-cyclodextrin (CD). This inclusion complex could further weaken the aggregation-induced emission (AIE) effect remarkably. This advance paves the way to introduce AIE property into molecular devices applications.