通过不对称氢转移/动态动力学拆分合成碳环N^3-嘌呤核苷

N^3-嘌呤核苷由于可能同时被嘌呤和嘧啶代谢酶识别,因而有望作为双靶点药物应用于抗病毒治疗.报道了一种以α-(N^3-嘌呤)取代的环烷酮为原料,通过不对称氢转移反应实现动态动力学拆分,高收率高立体选择性地合成系列碳环N^3-嘌呤核苷化合物.该催化体系也适用于α-嘧啶取代的环烷酮底物,且产物通过进一步衍生,合成了2’-F-,Ac S-,N^3-修饰的碳环嘧啶核苷.     

Effects of flame‐retardant ramie fiber on enhancing performance of the rigid polyurethane foams

Ramie fiber (RF) with excellent tensile strength was treated by a flame retardant and obtained the modified RF (MRF) that is incombustible. Then, MRF was used to improve the performance of rigid polyurethane foams (RPUF). The mechanical properties of the composite were investigated by compressive strength test and shear stress test. The fire characteristics were studied using a cone calorimeter. And the thermal decomposition and flammable properties were further evaluated using thermogravimetric analysis and limiting oxygen index. The results showed that MRF improve the mechanical properties of RPUF and eliminate the harm of flammability of RF on the RPUF.     

RuCl₃·3H₂O catalyzed reactions: facile synthesis of bis(indolyl)methanes under mild conditions

RuCl?·3H?O was found to be an effective catalyst for reactions of indoles, 2-methylthiophene, and 2-methylfuran with aldehydes to afford the corresponding bis(indolyl)methanes, bis(thienyl)methanes, and bis(fur-2-yl)methanes in moderate to excellent yields. Experimental results indicated that mono(indolyl)methanol is not the reaction intermediate under these reaction conditions.     

Effect of γ-radiation on ointment cold cream

In this paper, Co-60γ ray was used to irradiate the ointment cold cream at room temperature (25°C). We also used FTIR, GC and thin film chromatogram to analyse various irradiated samples. It was found that the ointment cold cream can be irradiated at dose of 5–35 kGy and at dose rate from 0.2 to 0.6 kGy/h at room temperature (25°C) without evident decomposition. At dose of 5–15 kGy, the number of bacteria can be reduced to hygienic standard value. The radiation sterilization is a safe method for killing the bacteria in the ointment cold cream.     

Photocontrolled Multidirectional Differentiation of Mesenchymal Stem Cells on an Upconversion Substrate

The effective guidance of mesenchymal stem cell (MSC) differentiation on a substrate by near‐infrared (NIR) light is particularly attractive for tissue engineering and regenerative medicine. However, most of current substrates cannot control multidirectional differentiation of MSCs like natural tissues. Herein, a photocontrolled upconversion‐based substrate was designed and constructed for guiding multidirectional differentiation of MSCs. The substrate enables MSCs to maintain their stem‐cell characteristics due to the anti‐adhesive effect of 4‐(hydroxymethyl)‐3‐nitrobenzoic acid modified poly(ethylene glycol) (P1) attached on the upconversion substrate. Upon NIR irradiation, the P1 is released from the substrate by photocleavage. The detachment of P1 can change cell–matrix interactions dynamically. Moreover, MSCs cultured on the upconversion substrate can be specifically induced to differentiate to adipocytes or osteoblasts by adjusting the NIR laser. Our work provides a new way of using NIR‐based upconversion substrate to modulate the multidirectional differentiation of MSCs.     

TiO_2/EDTA-rich carbon composites:Synthesis,characterization and visible-light-driven photocatalytic reduction of Cr(Ⅵ)

Ti02/EDTA-rich carbon composites(TiO_2/EDTA-RC) have been successfully synthesized via a low temperature carbonization process. TiO_2/EDTA-RC exhibits marked absorption of visible light and excellent photoreduction of Cr(Ⅵ) activity under visible light irradiation(λ420 nm). Due to the high carboxyl group content and strong coordination ability of EDTA, TiO_2-EDTA complex can be easily fabricated between EDTA incorporated in carbon sheet and titanol group on the surface of TiO_2. TiO_2-EDTA complexes on the surface of TiO_2/EDTA-RC, the LMCT complex, are responsible for the prominent photoreduction of Cr(Ⅵ) properties of Ti02/EDTA-RC under visible light irradiation. In addition, the unique structure ofTiO_2/EDTA-RC is also propitious to the visible-light photocatalytic reduction of Cr(Ⅵ).Carbon sheet of TiO_2/EDTA-RC acts as a supporter. TiO_2 nanoparticles and EDTA homogeneously disperse into the carbon sheet supporter and form the TiO_2-EDTA complexes, which can avoid the aggregation of TiO_2 nanoparticles in the aqueous solution and provide more photocatalytic reaction points for the reduction of Cr(Ⅵ).     

A dual chemosensor for Cu2+ and Fe3+ based on π-extend tetrathiafulvalene derivative

A new dual chemosensor (TTF-PBA) for Fe³⁺ and Cu²⁺ in different signal pathways was designed and synthesized. The absorption spectrum, fluorescence spectrum and cyclic voltammograms changed in the presence of Cu²⁺ and Fe³⁺. The optical color changed within 5 s from yellow to orange upon the addition of Cu²⁺, and it changed to dark yellow when Fe³⁺ existed. The cyclic voltammogram of Cu²⁺/TTF-PBA changed from E_ox = 0.50 V, E_red = 0.32 V to E_ox = 0.64 V, E_red = 0.80 V (vs Ag/AgCl) upon the addition of 2.0 equiv. Cu²⁺. As for Fe³⁺/TTF-PBA, its oxidation wave disappeared, and its reduction wave appeared at E_red = ?0.59 V (vs Ag/AgCl) upon the addition of 4.0 equv. Fe³⁺. The sensor displayed high selectivity for Cu²⁺ and Fe³⁺ over other ions including Pb²⁺, Zn²⁺, Ni²⁺, Ag⁺, Cr³⁺, Mn²⁺, Al³⁺, Co²⁺, Pd²⁺, Hg²⁺, Fe^2+, Cd²⁺, Ce³⁺, Bi³⁺ and Au³⁺, the detection limits for Cu²⁺ and Fe³⁺ ion reached as low as 5.33 × 10^?7 mol/L and 5.34 × 10^?7 mol/L, respectively. Furthermore, when Fe³⁺ existed, Cu²⁺ can be detected sequentially by the sensor through the absorption spectrum and the color change observed by naked-eyes.     

藻类肝毒素的富集提取与分离

采用固相萃取（SPE）和高效液相色谱法（HPLC）对蓝绿藻肝毒素进行富集与分离。以悦目颤藻为研究对象,选择最佳方式破坏其细胞,使其释放出细胞内肝毒素,对肝毒素进行SPE富集提取。用反相HPLC技术,以C18柱作分离术,32%乙腈-水（含0.01mol/L乙酸铵）为流动相,达到了对藻类肝毒素的良好分离。     

微量热法研究过氧化氢酶底物抑制动力学

过氧化氢酶是需氧生物体内抗氧化酶系的重要组分。过氧化氢酶催化过氧化氢分解是一个两底物酶促反应,依照Chance提出的机理,反应速率方程具有一级反应方程的形式。此反应在高浓度底物存在的情况下,表现出明显的不可逆底物抑制。本研究用热动力学方法研究了这一反应,提出了一种不可逆底物抑制机理,并应用该机理求出了相关动力学参数。在310.15K,pH=7.0时k0=9.6×10^5L·mol^-1^·s^-1,k1/k2=2.9×10^6。实验结果证明此机理正确有效。