Design and Synthesis of 3‐Aryl‐5‐Alicylic‐[1,2,4]‐oxadiazoles as Novel Platelet Aggregation Inhibitors

A series of 4‐[2‐(alicyclic‐[1,2,4]oxadiazol‐3‐yl)phenoxy]‐butyric acids were synthesized from N‐hydroxy‐2‐isopropoxy benzamidine in 4 steps with good yields. These [1,2,4]oxadiazoles are novel platelet aggregation inhibitors preventing human platelet aggregation induced by thromboxane derivative U44,619 and adenosine diphosphate. A structure‐activity‐relationship study revealed that the potency for these 5‐oxadiazoles increases with the increase in the ring size of the alicylic rings. Derivative 8f may be useful as a template for the design of more potent anti‐platelet agents.     

纳秒强激光场中苯电离产生高价离子的研究

用25 ns脉冲Nd-YAG 532 nm的激光，在1010～1011 W•cm－2的光场强度下，利用飞行时间质谱对He、 N2、Ar载气条件下苯的激光电离过程进行了研究.发现当利用氩作为载气时，除观察到C2＋、C2H2+、C3H3+、C6H6+离子外，还观察到很强的Cq＋(q=1～3)高价离子.这些离子都有很高的平动能， C2＋的最可几平动能为12.9 eV， C3＋为37.5 eV.通过改变载气种类和压力及在不同光场强度条件下的实验，可以认为这些高价离子来源于含苯团簇的库仑爆炸过程.     

Tuning the solid-state emission of the analogous GFP chromophore by varying alkyl chains in the imidazolinone ring

New analogues of green fluorescent protein (GFP) chromophore mGFP-Cn (n = 1, 3, 5, 11) with alkyl chains of different lengths in the imidazolinone rings were synthesized and their crystal structures were determined. These GFP-like chromophores are all emissive in the solid state. And the solid-state emission quantum yields of increase by extending the lengths of alkyl chains, owing to the fact that the intermolecular pi-pi interactions are significantly weakened based on their crystal structures.     

微通道周期流动电位势及电粘性效应

求解了双电层的Poisson-Boltzmann方程和流体运动的Navier-Stokes方程,得到在周期压差作用下,二维微通道的周期流动电位势,流动诱导电场和液体流动速度的解析解．量纲分析表明,流体电粘性力与以下3个参数有关:1) 电粘性数,它表示定常流动时,通道最大电粘性力与压力梯度的比;2) 形状函数,它表示电粘性力在通道横截面的分布形态; 3) 耦合系数,它表示电粘性力的振幅衰减特征和相位差．分析结果表明,微通道周期流动诱导电场、流动速度与频率Reynolds数有关．在频率Reynolds数小于1时,流动诱导电场随频率Reynolds数变化很慢．在频率Reynolds数大于1时,流动诱导电场随频率Reynolds数的增加快速衰减．在通道宽度与双电层厚度比值较小情况下,电粘性效应对周期流动速度和流动诱导电场有重要影响．     

基于多光谱图像融合的掌纹识别方法

生物特征识别在信息安全领域发挥着重要作用,掌纹识别作为一种新型生物特征识别方式,具有低失真、非侵入性和高唯一性等优势。传统掌纹研究大多使用自然光成像系统以灰度格式获取,识别精度很难进一步提升。为了获得更多的身份鉴别信息,提出利用多光谱掌纹图像代替自然光掌纹图像。针对现有掌纹识别算法由于没有考虑到不同光谱的特性而导致纹理细节丢失,识别精准率低的问题,提出了一种基于多光谱图像融合的掌纹识别算法。该方法通过对不同光谱下的掌纹图像进行快速自适应二维经验模式分解（FABEMD）,将多光谱掌纹图像分解成一系列频率由高到低的二维固有模态函数(BIMF)和一个残余分量,残余分量可被视为该光谱图像低频信息的初步估计。图像采集过程中光照条件很难保持稳定,而近红外光谱图像在进行FABEMD分解时对光照变换敏感,容易导致分解后的BIMF背景信息过于冗余;因此对分解后的近红外掌纹图像进行背景重建及特征细化,在对背景冗余信息进行平滑处理的同时可以有效增强高频信息的特征表达。为避免直接融合处理后引发的图像过度曝光问题,提出对近红外特征压缩后再融合。此外,提出了一种结合了注意力机制的改进残差网络（IRCANet）,用于融合后的掌纹图像分类,在网络中引入分阶段残差结构,缓解了网络的退化问题,在学习过程中有效地减少信息丢失,对于融合后的多光谱掌纹图像,分阶段残差结构能够稳定地将图像信息在网络间传输,但对图像中的高低频信息区分效果不够显著,为了使网络关注更多区分性特征,利用特征通道间的相互依赖性,在分阶段残差结构中结合了通道注意力(Channel Attention)机制。最终,在香港理工大学（PolyU）多光谱掌纹数据集上进行的综合实验表明,该方法可以取得良好的效果,算法识别准确率能达到99.67%且具有良好的实时性。     

Quinone imine dye formation via photocycloaddition between isocyanates and chloranil

Photochemical [2+2]cycloaddition between electron-donating aryl isocyanates and chloranil was observed in acetonitrile or benzene, and the following elimination of carbon dioxide resulted in the formation of the corresponding quinone imine dyes. This new route for synthesis of quinone imine was investigated by product analyses, laser flash photolyses, and molecular orbital calculation.     

Total synthesis of (+/-)-morphine

[Structure: see text] The morphinan skeleton was effectively synthesized by an intramolecular Mannich-type reaction. Further transformation led to total synthesis of morphine.     

Factors that regulate the conformation of m-benziporphodimethene complexes: agostic metal-arene interaction, hydrogen bonding, and η2,π coordination

Group 12 and silver(I) tetramethyl‐m‐benziporphodimethene (TMBPDM) complexes with phenyl, methylbenzoate, or nitrophenyl groups as meso substituents were synthesized and fully characterized. The dimeric silver(I) complex displays an unusual η²,π coordination from the β‐pyrrolic C?C bond to the silver ion. All of the complexes displayed a close contact between the metal ion and the inner C(22)? H(22) on the m‐phenylene ring. The downfield chemical shifts of H(22) and large coupling constants between Cd^II and H(22) strongly support the presence of an agostic interaction between the metal ion and inner C(22)–H(22). Crystal structures revealed that the syn form is the predominant conformation for TMBPDM complexes. This is distinctively different from the exclusive anti conformation observed in m‐benziporphyrin and tetraphenyl‐m‐benziporphodimethene (TPBPDM) complexes. Evidently, intramolecular hydrogen‐bonding interactions between axial chloride and methyl groups stabilize syn conformations. Unlike the merely syn conformation observed in the solid‐state structures of TMBPDM complexes that contain an axial chloride, in solution these complexes display highly solvent‐ and temperature‐dependent syn/anti ratio changes. The observation of dynamic ¹H NMR spectroscopic scrambling between syn and anti conformations from the titration of chloride ion into the solution of the TMBPDM complex suggests that axial ligand exchange is a likely pathway for the conversion between syn and anti forms. Theoretical calculations revealed that intermolecular hydrogen‐bonding interactions between the axial chloride and CHCl₃ stabilizes the anti conformation, which explains the increased ratio for the anti form when dichloromethane or chloroform was used as the solvent.     

Analysis of baicalein, baicalin and wogonin in Scutellariae radix and its preparation by microemulsion electrokinetic chromatography with 1-butyl-3-methylimizolium tetrafluoborate ionic liquid as additive

Microemulsion electrokinetic chromatography (MEEKC) using 1-butyl-3-methylimidazolium tetrafluoroborate (BMIM-BF4) ionic liquid (IL) as additive was developed for the analysis of baicalin, wogonin and baicalein in Scutellariae radix and its preparation. After conducting a series of optimizations, baseline separation was obtained for the analytes within 5min under the optimum conditions (sodium dodecyl sulfate (SDS) 0.88% (m/v) ethyl acetate 0.8% (v/v) butan-1-ol 0.2% (v/v) and the buffer composition were 25% acetonitrile (v/v), 7.5 mM BMIM-BF4 and 10 mM NaH2PO4, pH 8.2, applied voltage 17.5 kV and detection at 254 nm), the method has been successfully applied to the determination and quantification of the analytes in the extracts of S. radix (cooked), S. radix (raw) and Qingfeiyihuowan which was the preparation including S. radix.