Preparation of mesoporous alumina with large pore size and their supported rhenium oxide catalysts in metathesis of 1-butene and 2-butene to propene

Mesoporous γ-aluminas with large pore size(up to 19 nm,denoted as MA19) are prepared from dispersed pseudo-boehmite using pluronic P123 as template.It is found that these mesoporous alumina supported rhenium oxide catalysts were more active and have far longer working life-span in gas-phase metathesis of 1-butene and 2-butene to propene than rhenium oxide on conventional alumina with small pore size(5 nm).At 60°C and atmospheric pressure with WHSV = 1 h-1,the similar stable conversions of butene(ca.55%) for all the 13 wt% Re 2 O 7 /alumina catalysts were obtained near the chemical equilibrium,and the stable working life-spans of Re 2 O 7 /MA19 were far longer than that of Re 2 O 7 /Al 2 O 3,being about 70 h and 20 h,respectively.     

Localized Chemical Remodeling for Live Cell Imaging of Protein‐Specific Glycoform

Live cell imaging of protein‐specific glycoforms is important for the elucidation of glycosylation mechanisms and identification of disease states. The currently used metabolic oligosaccharide engineering (MOE) technology permits routinely global chemical remodeling (GCM) for carbohydrate site of interest, but can exert unnecessary whole‐cell scale perturbation and generate unpredictable metabolic efficiency issue. A localized chemical remodeling (LCM) strategy for efficient and reliable access to protein‐specific glycoform information is reported. The proof‐of‐concept protocol developed for MUC1‐specific terminal galactose/N ‐acetylgalactosamine (Gal/GalNAc) combines affinity binding, off‐on switchable catalytic activity, and proximity catalysis to create a reactive handle for bioorthogonal labeling and imaging. Noteworthy assay features associated with LCM as compared with MOE include minimum target cell perturbation, short reaction timeframe, effectiveness as a molecular ruler, and quantitative analysis capability.     

Study on the Constituents of Roots of Aceriphyllum rossii

A new stereoisomer of a tetrahydrofuranoid lignan, acerifuranoid A ( 1 ), and two new oleanane‐type triterpenoids, aceriphyllic acids J and K ( 2 and 3 ), were isolated from the roots of Aceriphyllum rossii. Their structures were elucidated on the basis of spectroscopic analyses and chemical evidence. These isolated compounds exhibited weak cytotoxic activity against various cancer cell lines with IC₅₀>150 μM .     

The computations of reflection coefficients of multilayer structure based on the reformulation of Thomson-Haskell method

A reformulation of the Thomson-Haskell method is presented for calculating the reflection coefficients of multilayer structure immersing in the coupling fluid. Instead of directly multiplying the layer propagator matrix, the new method splits the layer propagator matrix and excursively determines the interface stiffness matrix starting from the bottom half-space with known stiffness. A formulation for the reflection coefficients is derived based on the obtained interface stiffness matrix of the top layer. This scheme can be applied to a single solid layers or layered structures containing both fluid and solid layers. It keeps the simplicity but naturally excludes the exponential growth term and thus can be applied at any frequency range. Its validity and feasibility were experimentally proved by the measurement of the reflection coefficients of a three layered structure of aluminum–glass–aluminum and a sandwiched layer structure of two 250 μm stainless plates filled with 100 μm deionized water based on the inversion of V(z, t) technique. The result of experiments is consistent with the theoretical calculation. The reformulation of the Thomson-Haskell method offers an efficient and effective solution for calculating the acoustic reflection coefficients of multilayer structures of any configurations.     

Formation of Columnar Liquid Crystals on the Basis of Unconventional Triazine‐Based Dendrimers by the C3‐Symmetric Approach

Two series of unconventional triazine‐based dendrimers with C₂ symmetry and C₃ symmetry were prepared. The newly prepared C₃‐symmetrical dendrimers were characterized by ¹H and ¹³C NMR spectroscopy, mass spectrometry, and elemental analysis. Differential scanning calorimetry, polarizing microscopy, and powder XRD showed that the C₃‐symmetrical dendrimers display columnar liquid‐crystalline phases during thermal treatment, but the C₂‐symmetrical dendrimers were not observed to behave correspondingly. The molecular conformations of C₃‐ and C₂‐symmetrical dendrimers were obtained by computer simulation with the MM2 model of the CaChe program in the gas phase. The simulation results reasonably explain the different mesogenicities of C₃‐ and C₂‐symmetric dendrimers. This new strategy should be applicable to other types of unconventional dendrimers with rigid frameworks for displaying columnar liquid‐crystalline behavior.     

Synthesis and Spectroscopic Characteriration of Transition MetalComplexes of Maleionitriledithiolene and 1,10-Phenanthroline

Thedithiolenesanddiiminesandtheirmetalcomplexesareanimportantresearchfieldintheorganicandcoordinationchemistry'-'.Metalcomplexesofadithioleneandadiiminehaveexcellentelectronicfullctionsduetotheintramolecularchargetransferfromaligandtootherligand(LL'C...     

Diode-pumped actively Q-switched Tm:YAG ring laser operation at room temperature

2-μm lasers with high pulse energy and long pulse width of hundreds of nanoseconds are needed urgently in the accurate wind velocity lidar systems. This paper presents the acoustic-optical Q-switched Tm:YAG laser performance in a pulsed-laser-diode end-pumping figure-eight ring resonator structure. Pulse energy and pulse width are investigated with the increasing of the incident pump energy at different repetition rate operation. Maximum energy of 4.6 mJ with the pulse width of 179.2 ns and 3.57 mJ with pulse width of 184.4 ns are obtained at the repetition rate of 20 and 100 Hz, respectively. Under free-running and Q-switched operation, the peak output wavelength is 2.014 μm at all time, and the beam quality factors are lower than 2 times diffraction-limited measured by a knife-edge traveling method.     

Localized Chemical Remodeling for Live Cell Imaging of Protein-Specific Glycoform

Live cell imaging of protein-specific glycoforms is important for the elucidation of glycosylation mechanisms and identification of disease states. The currently used metabolic oligosaccharide engineering (MOE) technology permits routinely global chemical remodeling (GCM) for carbohydrate site of interest, but can exert unnecessary whole-cell scale perturbation and generate unpredictable metabolic efficiency issue. A localized chemical remodeling (LCM) strategy for efficient and reliable access to protein-specific glycoform information is reported. The proof-of-concept protocol developed for MUC1-specific terminal galactose/N-acetylgalactosamine (Gal/GalNAc) combines affinity binding, off-on switchable catalytic activity, and proximity catalysis to create a reactive handle for bioorthogonal labeling and imaging. Noteworthy assay features associated with LCM as compared with MOE include minimum target cell perturbation, short reaction timeframe, effectiveness as a molecular ruler, and quantitative analysis capability.     

Formation of Hybrid Perovskite Tin Iodide Single Crystals by Top‐Seeded Solution Growth

Hybrid perovskites have generated a great deal of interest because of their potential in photovoltaic applications. However, the toxicity of lead means that there is interest in finding a nontoxic substitute. Bulk single crystals of both cubic CH₃NH₃SnI₃ and CH(NH₂)₂SnI₃ were obtained by using the top‐seeded solution growth method under an ambient atmosphere. Structural refinement, band gap, thermal properties, and XPS measurements of CH₃NH₃SnI₃ and CH(NH₂)₂SnI₃ single crystals are also reported in detail. These results should pave the way for further applications of CH₃NH₃SnI₃ and CH(NH₂)₂SnI₃.