The 1,3-Dipolar Cycloadditions of Nitrile Oxides and Nitrile Imines to Alkyl Dicyanoacetates

The readily available alkyl dicyanoacetates 1 reacted with the 1,3-dipolar reagents arenecarbonitrile oxides 2 ′ and arenecarbonitrile imines 5 ′ to afford 1,2,4-oxadiazol and 1,2,4-triazol derivatives. The arenecarbonitrile oxides 2 ′ with electron-donating groups on the arene ring gave products 3a – d resulting from addition on both CN groups of 1 , and those with electron-withdrawing groups provided mono-adducts 4a – e (Scheme 1). Arylnitrile imines 5 ′ reacted with 1 to offer both bis- and mono-addition products (Scheme 2); the bis-adducts 8a , b possess an ester structure, whereas the mono-adducts 6a – d present a ketene-hemiacetal structure.     

Rapid determination of underivatized pyroglutamic acid, glutamic acid, glutamine and other relevant amino acids in fermentation media by LC-MS-MS

Determination of amino acids in a complex matrix without derivatization is advantageous, however, difficulties are found in both the detection and the separation of those compounds. In this study, a rapid and reliable LC-MS-MS method for the quantitation of underivatized amino acids in exocellular media was established. Injections were made directly after centrifugation of the samples, without further preparation. The separation of seven underivatized amino acids was achieved on a reversed-phase C18 column with pentadecafluorooctanoic acid as a volatile ion-pair reagent, and the specific detection of most amino acids was achieved by MS-MS of the specific transitions [M + H]+-->[M + H - 46]+. The calibration curves of all analytes were linear over the range of 1.0-1000 microg ml(-1) and the detection limits ranged from 0.1 to 5 ng ml(-1), with an injection volume of 20 microl. The inter-day and intra-day precisions ranged from 2.6 to 5.7% and 4.8 to 8.2%, respectively; the mean recoveries of the seven analytes were 81-104%, 91-107% and 93-101% respectively at the spiked level of 10, 40 and 200 microg ml(-1). A large number of fermentation samples were analysed using this method. The technique is simple, rapid, selective and sensitive, and shows potential for the high-throughput quantitation of amino acids from other biological matrices.     

Sc(OTf)3-catalyzed efficient synthesis of beta,beta-bis(indolyl) ketones by the double indolylation of acetic acid 2-methylene-3-oxobutyl ester

In the presence of 5 mol% Sc(OTf)3, double indolylation of acetic acid 2-methylene-3-oxo-butyl ester with differently substituted indoles readily afforded beta,beta-bis(indolyl) ketones. The reaction may proceed via a Sc(OTf)3-catalyzed SN2'-type substitution and subsequent conjugate addition.     

Decomposition Reaction of Zn-MPA（3-Mercaptopropionic Acid） Complex Under Microwave Irradiation

The thermal decomposition of Zn-MPA complex was investigated under microwave irradiation. ZnO and ZnS nanocrystals could be obtained by decomposing Zn-MPA（3-mercaptopropionic acid） complex under different reaction conditions. It was found that both the pH value of the solution and the molar ratio of Zn2＋ and MPA can play an important role in the formation of ZnO and ZnS nanocrystals. MPA mainly acts as an S source or as a complexing agent. This study provides a new route for the controllable preparation of semiconductor nanocrystals.     

非晶态NdxT1-x(T=Fe,Co,Ni)薄膜的低温磁性

本文讨论了非晶态Nd_xT_1-x(T=Fe,Co,Ni)薄膜为滋结构,以及在低温下磁化强度随温度变化的反常特性,在20K附近观测到磁化强度有陡降现象,并且在较大的成份范围内所对应的温度基本不变,我们认为,在这类非晶态合金中,当Nd含量超过一定值后,其磁中性态(通称基态)可能同时是散反铁磁性和散铁磁性的共存态,在20K附近的磁化强度发生陡降,是散反铁磁性←→顺磁性相转变的反映,这两种磁结构共存的临界成份相应约为:Nd-Fe情况x≥0.45;Nd-Co,x≥0.20;Nd-Ni,x≥0.08。 关键词：     

半无限超晶格的原子均方位移

本文在简立方晶体的简单模型下,应用格林函数方法计算了半无限超晶格中的原子均方位移,并讨论了表面和界面对晶格振动的效应。 关键词：     

STRUCTURES OF Si AND Ge CLUSTERS UNDER MODIFIED STILLINGER-WEBER POTENTIAL

Structural behaviors of silicon and germanium clusters under the recently proposed modified Stillinger-Weber (SW) potential have been studied by molecular dynamics method along with the con-jugate-gradient optimization. Since the SW potentials have been derived from the properties of bulk materials, it gives relatively large discrepancy when the cluster number is small, e.g. n=3 and 4. When n>4, the ground-state structures under the modified SW potential are close to that from the first-principle calculation. The binding energies are also improved under the modified SW potential. These results may be attributed to the relative enhancement of the two-body term over the three-body term in the modified SW potential, which leads to structures with a preferential coordination number 4. Structural behaviors of germanium clusters are similar to those of silicon.     

翘嘴鳜铜锌超氧化物歧化酶基因的分子克隆与原核表达

运用RT-PCR和RACE-PCR技术克隆了翘嘴鳜(Siniperca chuatsi)铜锌超氧化物歧化酶(命名为ScCu/Zn-SOD)基因,该基因的cDNA序列全长为804bp,开放阅读框为465bp,编码154个氨基酸。氨基酸序列中含2个Cu/Zn-SOD标签序列、7个铜锌金属结合位点、2个半胱氨酸位点和1个N-糖基化位点;其与胞内Cu/Zn-SOD(icCu/Zn-SOD)和胞外Cu/Zn-SOD(ecCu/Zn-SOD)氨基酸序列的同源性分别为60.13%~92.21%和33.77%~42.21%。在系统进化树中,ScCu/Zn-SOD与其它物种的icCu/Zn-SOD聚成一支。ScCu/Zn-SOD的蛋白晶体结构主要由2个α螺旋和8个β折叠组成,呈β折叠构象,通过结合1个Cu2+和1个Zn2+构成其酶活性中心。ScCu/Zn-SOD的mRNA在翘嘴鳜肌肉、鳃、肝脏和肾脏等组织中均有表达,且鳃中的相对表达量最高。将该基因编码蛋白序列与pET-30a表达载体重组,热激转入大肠杆菌BL21(DE3)感受态细胞中诱导表达,SDS-PAGE检测发现诱导后菌液的超声上清中有可溶性重组蛋白表达。     

不同负荷下餐厨垃圾与水稻秸秆共消化厌氧产氢研究

进料负荷对餐厨垃圾与水稻秸秆混合厌氧发酵产氢过程有重要影响. 以进料负荷为影响因子, 设置温度均为55℃的餐厨垃圾与水稻秸秆混合厌氧发酵产氢实验, 其中进料负荷(以VS计)分别设置为(A)5kg?m-3?d-1、(B)10kg?m-3?d-1、(C)15kg?m-3?d-1, 分析厌氧产氢过程中产气量、产氢速率、pH、VFAs、氨氮、SCOD等参数的变化. 实验结果表明: B组发酵底物产气量最大, 为8664mL, 产氢速率也最大, 为748.3mL?h-1, 反应过程中pH始终维持在5.5±0.1内, 是厌氧产氢的最佳范围. 实验结束时, 各组VFAs、氨氮浓度分别为7292.46、8248.35、8558.24mg?L-1和544.48、754.31、1458.33mg?L-1. 同时各组SCOD浓度变化趋势相似. 在研究范围的最佳进料负荷下, 进行回流比分别为10%、30%、50%的实验, 结果显示30%回流比的产氢量最大, 为56039mL, 同时运行过程中系统稳定性较好. 综上所述, 进料负荷为10kg?m-3?d-1, 30%回流比的餐厨垃圾与水稻秸秆混合厌氧发酵产氢时, 微生物活性较好, 能够产生更多的氢气. 这一结果可为餐厨垃圾资源化提供参考依据.     

光场显微镜实现裸眼三维实时显示

提出了一种将光场显微镜与裸眼三维显示技术相结合的方法,实现了利用光场显微镜对微观样品进行三维裸眼实时观察的技术。该技术将光场显微镜得到的子图像阵列直接投影在微透镜阵列的焦平面上,在空间一定区域内双眼可分别观看到两幅不同视角图像,使观察者产生立体视觉。该系统具有结构简单,无需相干光源,无需佩戴特殊眼镜,可多人同时观看等优点,应用前景广泛。