Surfactant Mediated Microphase Separation in Miscible Block Copolymer of Poly(4-vinyl pyridine-b-hydroxybutylacrylate)

Chinese Journal of Polymer Science - Miscible disordered block copolymers (BCPs) are rarely studied due to the limits in self-assembly into ordered microstructures. Herein, we proposed a facile...     

Photodegradation mechanisms of acyclovir in water and the toxicity of photoproducts

Journal of Radioanalytical and Nuclear Chemistry - In the present work the final products of coumarin radiation chemical transformation are investigated by chromatography. During radiolysis of...     

An efficient method for the synthesis of gem-difluoroolefins

A series of gem-difluoroolefin derivatives were synthesized in moderate to good yields by the reaction of α,α-difluoro-β-carbonyl benzothiazol-2-yl sulfones (DFBTs) with various carbon nucleophiles. Using dl-proline as organocatalyst, the reaction of DFBT with acetone gave a tertiary alcohol, which could be further converted to the corresponding difluoroolefin by LDA.     

Iridium-catalyzed annulation between 1,2-diarylethanone and 3-aminopropanol toward site-specific 2,3-diaryl pyridines

An iridium-catalyzed annulation between 1,2-diarylethanone and 3-aminopropanol was developed, leading to site specific 2,3-diarylpyridines in moderate yields. 3-Aminopropanol served as both a four-atom component and solvent during this procedure, releasing water as a clean by-product. The reaction may proceed with sequential imine formation, alcohol oxidation and intramolecular cyclization by Knoevenagel reaction.     

Asymmetric aza-Henry reaction of fluoromethylated imines catalyzed by cinchona-derived bifunctional thiourea

The asymmetric aza-Henry reaction of fluoromethyl imines derived from 4-methoxyaniline with nitromethane was achieved under mild conditions using cinchona-derived bifunctional thiourea as catalyst. A series of chiral fluoromethylated β-nitroamines were synthesized and their transformation to optically pure 4-fluoromethyl-2-imidazolidones was illustrated.     

HIV蛋白酶抑制剂——利迪链菌素的分子对接研究

用分子对接的方法, 对利迪链菌素的抗HIV蛋白酶活性进行了研究. 为了更准确地反映利迪链菌素分子与酶蛋白结合的情况, 充分考虑受体活性部位的柔性, 采用了FlexX(初步对接)和Flexidock(精确对接)分两步将配体与受体进行对接. 在初步对接中, 设计了不同的受体活性部位来考察是否有结合水分子参与抑制剂与酶的结合. 对一种作用方式已知的非肽类HIV蛋白酶抑制剂Aha006进行的对接研究显示, 分子模拟的结果与实际情况吻合得较好, 证明了本文所采用的方法的可靠性. 利迪链菌素与蛋白酶活性部位的对接结果显示, 配体分子与受体之间的结合没有结合水分子的参与, 两者通过5对氢键作用结合成为稳定的复合物. 利迪链菌素占据结合腔, 覆盖了蛋白酶的活性三联体Asp25-Thr26-Gly27, 从而起到抑制其生物活性的作用.     

纳米铂直接修饰玻碳电极的制备及在半胱氨酸中的电化学行为

采用一步化学原位还原法将球形纳米铂颗粒直接修饰在玻碳电极上,用SEM、EDS和电化学方法对该电极进行表征并与铂片电极、裸玻碳电极进行了对比。结果表明,纳米铂修饰电极的峰电流与扫描速度呈线性关系,纳米铂在电极表面覆盖率为1.28×10-7mol/cm2。循环伏安法研究结果表明纳米铂修饰电极对半胱氨酸的催化氧化作用和铂片电极相比提高了数倍,且峰电位负移了0.3V。在纳米铂修饰的玻碳电极上,半胱氨酸的浓度在1.0×10-7mol/L到1.0×10-5mol/L范围内和催化电流呈线性关系。     

高功率,红光至中红外可调谐腔内和频光学参量振荡器

本文利用高重复频率,高平均功率大模场面积飞秒光纤激光器作为同步抽运源,抽运以多周期极化掺氧化镁铌酸锂为非线性晶体的单共振光学参量振荡器,获得了高功率可调谐红光至中红外光,信号光调谐范围为1450—2200 nm,闲频光调谐范围为2250—4000 nm,在2 W的抽运功率下,信号光输出波长为1502 nm时获得最大输出功率374 mW,转换效率为18.7%,脉冲宽度为144 fs,此时中红外输出中心波长为3.4μm,平均功率为166 mW.再利用BBO晶体对信号光进行腔内和频,获得和频光输出波长调谐范围为610—668 nm,在4.1 W抽运的情况下,最高平均功率为615 nm处的694 mW,转换效率达16.9%.     

水下平台对卫星上行激光通信研究

在合理选择通信系统参量和通信信道参量的基础上,利用Monte Carlo方法模拟了卫星接收到的水下平台上行激光通信信号.分析了卫星接收信号的空间和时间分布特性,以及与望远镜接收视场角的关系,并计算了接收信号的信噪比,得出了3°望远镜视场角和15 μs信号积分时间的优化参量.基于计算结果,根据激光脉冲的PPM调制方式和最大似然检测方法,计算了系统的通信误码率,同时分析了海气界面、云等传输介质对通信的影响.研究结果表明:根据文中给定通信系统参量,在典型海水、海气界面、云等环境条件下,卫星与激光信号中心水平距离5 km范围内信号误码率<10－4.因此位于水下60 m的水下平台可能实现对卫星上行激光通信.