胆碱与谷氨酸共价单层混合修饰玻碳电极的制作与表征及其测定亚硝酸根的分析应用

A choline and L-glutamic acid mixed monolayer covalently modified glassy carbon electrode (Ch-Glu/GCE) was fabricated and characterized by X-ray photoelectron spectroscopy (XPS), electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). It provided an excellent example of mixed covalent monolayer modification of carbon electrodes with alkanol and amino acid, and also a facile means for altering the interfacial architecture. The Ch-Glu/GCE displayed good catalytic activity toward the oxidation of nitrite anions. Differential pulse voltammetry was used for determination of nitrite at the Ch-Glu/GCE. The Ch-Glu/GCE showed higher capability for restraint of pollutions than a simple Ch modified electrode or a simple Glu modified electrode.     

激光驱动晶体发射高次谐波的特性研究

通过数值模拟激光驱动下电子在周期性势阱中的动力学行为, 研究了晶体在激光场中发射高次谐波的特性. 研究发现在一定的激光波长和光强驱动下, 晶体发射的谐波谱会呈现出双平台结构, 经分析后得知第一个平台主要来自于最低导带与价带间的电流(电子-空穴对复合), 第二个平台主要来源于较高导带与价带间的电流(电子-空穴对复合), 且两个平台的截止位置处的能量都与激光场的振幅呈线性关系. 在少周期激光驱动下, 晶体谐波第二平台的截止位置与激光的载波相位呈单调变化, 由此我们提出可以利用晶体谐波第二平台的截止位置来确定少周期激光的载波相位. 进一步研究发现, 在啁啾激光驱动下, 晶体发射谐波谱的第二平台有较大变化, 第二平台的发射效率会随啁啾参数而改变, 能够通过改变啁啾激光场来提高晶体谐波第二平台的发射效率.     

Visible-light-mediated selective thiocyanation/ipso-cyclization/oxidation cascade for the synthesis of thiocyanato-containing azaspirotrienediones

A visible-light-mediated metal-free thiocyanate radical addition/ipso-cyclization/oxidation cascade reaction for the synthesis of thiocyanato-containing azaspirotrienediones from N-phenylpropynamides is described. Cheap and readily available ammonium thiocyanate was used as a precursor to the thiocyanate free radical, which undergoes a radical addition reaction with the alkyne, followed by selective ipso-cyclization and oxidation to afford the dearomatized products. No product of ortho-cyclization was detected. The reaction completes the synthesis of C–S, C–C, and CO bonds in one pot, with abundant and renewable air oxygen as the sole sacrificial reagent and oxygen source.     

Preparation and time-gated luminescence bioimaging application of ruthenium complex covalently bound silica nanoparticles

Luminescent ruthenium(II) complex covalently bound silica nanoparticles have been prepared and used as a probe for time-gated luminescence bioimaging. The new nanoparticles were prepared by copolymerization of a luminescent Ru(II) complex tris(5-amino-1,10-phenanthroline)ruthenium(II) conjugated with 3-aminopropyl(triethoxy)silane (APS-Ru conjugate), free (3-aminopropyl)triethoxysilane (APS) and tetraethyl orthosilicate (TEOS) in a water-in-oil reverse microemulsion consisting of Triton X-100, n-octanol, cyclohexane and water in the presence of aqueous ammonia. Characterization by transmission electron microscopy indicates that the nanoparticles are monodisperse, spherical and uniform in size, 64 ± 4 nm in diameter. Compared with the dye-doping nanoparticles, dye leakage of the new nanoparticles was remarkably decreased. In addition, it was found that the Ru(II) complex luminescence could be effectively enhanced with a longer luminescence lifetime (∼2.3 μs) after forming the nanoparticles, which enables the nanoparticles to be suitable as a bioprobe for time-gated luminescence bioimaging applications. The nanoparticle-labeled streptavidin was prepared and successfully used for time-gated luminescence imaging detection of an environmental pathogen, Giardia lamblia, with high specificity and sensitivity.     

Effect of turnoff time on characteristics of the output pulse in an AO Q-switched laser

A laser-end-diode-pumped actively Q-switched Nd:YVO₄ laser with acoustic-optic (AO) modulator is realized. By changing the position of AO in the cavity for changing the transit time of the acoustic-wave, the effect of the AO turnoff time on the characteristics of the output Q-switched pulse is obtained. The experimental results show that the longer transit time leads to the wider pulse duration. By considering the Gaussian spatial distribution of the intra-cavity photon density and the AO turnoff time including the electronic turnoff time and the transit time of the acoustic-wave, the numerical solutions of the coupled Q-switched rate equations are consistent with the experimental results.     

Gear-like array of （H2O）12 as building blocks one-dimensional supramolecular assembly

The preparation and crystal structure of complex Co（Hsae）2·2H2O （1, H2sae = N-salicylidene-2-iminoethanol） are reported. X- ray analysis revealed that every six Co（Hsae）2 forms a cyclic chip and every 12 water forms a novel gear-like cluster. Acting as building blocks, the gear-like water cluster and complex chip are connected in A-B fashion and extend into one-dimensional supramolecular chain. Hydrogen bond is the primary bridging force in the formation of supramolecular framework.     

Synthesis of transition-metal phosphides from oxidic precursors by reduction in hydrogen plasma

A series of transition metal phosphides, including MoP, WP, CoP, Co₂P, and Ni₂P, were synthesized from their oxidic precursors by means of hydrogen plasma reduction under mild conditions. The effects of reduction conditions, such as metal to phosphorus molar ratio, power input, and reduction time, on the synthesis of metal phosphides were investigated. The products were identified by means of XRD characterization. It is indicated that metal phosphides were readily synthesized stoichiometrically from their oxides in hydrogen plasma under mild conditions.     

HIF in Gastric Cancer: Regulation and Therapeutic Target

HIF means hypoxia-inducible factor gene family, and it could regulate various biological processes, including tumor development. In 2021, the FDA approved the new drug Welireg for targeting HIF-2a, and it is mainly used to treat von Hippel-Lindau syndrome, which demonstrated its good prospects in tumor therapy. As the fourth deadliest cancer worldwide, gastric cancer endangers the health of people all across the world. Currently, there are various treatment methods for patients with gastric cancer, but the five-year survival rate of patients with advanced gastric cancer is still not high. Therefore, here we reviewed the regulatory role and target role of HIF in gastric cancer, and provided some references for the treatment of gastric cancer.