多偏振飞秒激光制备彩色铁

采用四个不同偏振方向的线偏振和圆偏振态飞秒激光扫描处理金属铁表面来制备不同的彩色铁。从不同角度观察被处理区域时,线偏振扫描处理的彩色区域呈现不同的色彩,而圆偏振扫描处理的区域没有明显的颜色变化。扫描电子显微镜图片显示,线偏振激光扫描处理金属铁表面形成了nm量级的激光诱导周期表面结构,其方向始终与激光偏振方向垂直;圆偏振激光扫描处理金属铁表面形成的条纹结构不明显且有大量的纳米颗粒结构。     

Effective control of photoluminescence from ZnO nanowires by a-SiN_x:H decoration

The a-SiN_x:H with a large bandgap of 3.8 eV was utilized to decorate ZnO nanowires. The UV emission from the a-SiN_x:H-decorated ZnO nanowires are greatly enhanced compared with the undecorated ZnO nanowire. The deep-level defect emission has been completely suppressed even though the sample was annealed at temperatures up to 400 °C. The incorporation of H and N is suggested to passivate the defect states at the nanowire surface and thus result in the flat-band effect near ZnO surface as well as reduction of the nonradiative recombination probability.     

全息光栅制作中光栅掩模形状随曝光量及干涉场条纹对比度的变化规律

为了在光栅制作中对光栅掩模占宽比及槽深加以控制,结合光刻胶在显影过程中的非线性特性,建立了光栅掩模槽形演化的数学模型,由此分析和模拟曝光量、条纹对比度对光栅槽形的影响。结果表明:在显影条件确定时,光栅掩模占宽比随光刻胶曝光量的增大而减小,条纹对比度减小,则不仅使光栅占宽比减小,同时也是使光栅槽深减小的主要原因,这样做的前提是预先通过实验和计算确定出一个曝光量上限Ec。该方法能够反映光栅掩模形状的演化规律,为全息光栅参数预测和工艺控制提供依据。     

Copper‐Catalyzed Deaminative Difluoromethylation

The difluoromethyl group (CF₂H) is considered to be a lipophilic and metabolically stable bioisostere of an amino (NH₂) group. Therefore, methods that can rapidly convert an NH₂ group into a CF₂H group would be of great value to medicinal chemistry. We report herein an efficient Cu‐catalyzed approach for the conversion of alkyl pyridinium salts, which can be readily synthesized from the corresponding alkyl amines, to their alkyl difluoromethane analogues. This method tolerates a broad range of functional groups and can be applied to the late‐stage modification of complex amino‐containing pharmaceuticals.     

One-pot synthesis of 3-(furan-2-yl)-4-hydroxy-2H-chromen-2-ones using K10 montmorillonite clay as heterogeneous catalyst

A facile and efficient one-pot synthesis of 3-(furan-2-yl)-4-hydroxy-2H-chromen-2-ones was developed. The reaction of ethyl 3-(2-hydroxyphenyl)-3-oxopropanoates and 2,5-dimethoxy-2,5-dihydrofuran were performed in presence of K10 Montmorillonite Clay heterogeneous catalyst under the solvent-free condition at 80?°C for 1?h, and followed by further converted to 3-(furan-2-yl)-4-hydroxy-2H-chromen-2-ones via refluxing in the alkaline EtOH solution for 0.5?h. The demonstrate method not only avoided the usage of any expensive transition-metals, but also eliminated the tedious intermediate purification. Moreover, due to the wide functional group tolerance, it could be applied to various substrates and gave product in good to excellent yields.     

超细二氧化锆的制备和表征

通过研究不同干燥条件下制得的二氧化锆的织构和结构，发现在超临界干燥过程中附加一定的惰性气体压力能够防止或大大减小凝胶在干燥过程中的收缩，从而可提高ＢＥＴ表面积，和普通空气中干燥得到的二氧化锆相比，超临界干燥得到的二氧化锆的孔结构大为改善。同时ＢＥＴ表面积地增大。     

用气相色谱、气相色谱－质谱对萘普生重要中间体6－甲氧基－2－乙酰萘合成反应的研究

在优良抗风湿药物萘普生的重要中间体６－甲氧基－２－乙酰素的合成中存在溶剂硝基苯的毒性及所带来的污染。而改用二氯乙烷作溶剂，只加少量硝基苯即可。为配合合成工艺的优化，用气相色谱（ＧＣ）、气相色谱－质谱（ＧＣ／ＭＳ）对反应产物、副产物及多个杂质进行了定性分析研究，并在５％ＯＶ－１０１ＣｈｒｏｍｏｓｏｒｂＷＡＷＤＭＣＳ柱上完成了产物的内标定量分析。从而减少了副反应和高沸点杂质的生成，最终生产出了９５％以上含量的６－甲氧基－２－乙酰萘产品，收率达到６０％。     

Asymmetric Synthesis XI: Stereoselective Synthesis of α-Alkyl-2-Furfurylamines Via d-Camphor Ketimine Intermediate

(R)-α-alkyl-2-furfurylamines (7), ranging from 5–67%d.e., are obtained by asymmetric alkylation of d-camphor ketimine (3). Using 1,3-diiodopropane and dibromoxylene as alkylating reagents, diimine derivatives (6f) and (6g) are formed. However, 1,2-dibromoethane gives coupling product (6h).     

Saturated absorption spectroscopy of buffer-gas-cooled Barium monofluoride molecules

We report an experimental investigation on the Doppler-free saturated absorption spectroscopy of buffer-gas-cooled Barium monofluoride (BaF) molecules in a 4 K cryogenic cell. The obtained spectra with a resolution of 19 MHz, much smaller than previously observed in absorption spectroscopy, clearly resolve the hyperfine transitions. Moreover, we use these high-resolution spectra to fit the hyperfine splittings of excited A(v = 0) state and find the hyperfine splitting of the laser-cooling-relevant A²Π_1/2(v = 0, J = 1/2,+) state is about 18 MHz, much higher than the previous theoretically predicted value. This provides important missing information for laser cooling of BaF molecules.     

Innentitelbild: Catalytic Asymmetric Functionalization of Aromatic C?H Bonds by Electrophilic Trapping of Metal‐Carbene‐Induced Zwitterionic Intermediates (Angew. Chem. 48/2014)

Asymmetric functionalization of aromatic C H bonds of N,N‐disubstituted anilines with diazo compounds and imines is reported for the efficient construction of α,α‐diaryl benzylic quaternary stereocenters in good yields with high diastereoselectivities and excellent enantioselectivities. This Rh^II/chiral phosphoric acid cocatalyzed transformation is proposed to proceed through a metal‐carbene‐induced zwitterionic intermediate which undergoes electrophilic trapping. To the best of our knowledge, this is the first asymmetric example of metal carbene‐induced intermolecular functionalization of aryl C H bonds.