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941.
942.
943.
Jian Chen Prof. Shanghui Chen Dongyu Lu Weihong Zhang Fangyan Xie Weiguang Xie Dr. Li Gong Chengxin Wang Prof. 《Chemphyschem》2010,11(12):2546-2549
Raman spectroscopic analysis is performed on WO3 nanowires at room temperature at pressures from ambient conditions to 45 GPa. Linear dependence of the first‐order Raman signal on various high‐pressure (HP) sections is observed. Upon increasing the applied pressure, the WO3 nanowires undergo four phase transitions at pressures around 1.7, 4.6, 21.5, and 26.2 GPa, which are all less than that reported for bulk WO3. When the pressure is up to 42.5 GPa, a new high‐pressure phase (HP5) appears. This phase has never been reported and is not reversible while unloading the pressure. 相似文献
944.
MicroRNAs are a recently identified class of small regulatory RNAs that target more than 30% protein-coding genes. Elevating evidence shows that miRNAs play a critical role in many biological processes, including developmental timing, tissue differentiation, and response to chemical exposure. In this study, we applied a computational approach to analyze expressed sequence tags, and identified 32 miRNAs belonging to 22 miRNA families, in three earthworm species Eisenia fetida, Eisenia andrei, and Lumbricus rubellus. These newly identified earthworm miRNAs possess a difference of 2-4 nucleotides from their homologous counterparts in Caenorhabditis elegans. They also share similar features with other known animal miRNAs, for instance, the nucleotide U being dominant in both mature and pre-miRNA sequences, particularly in the first position of mature miRNA sequences at the 5' end. The newly identified earthworm miRNAs putatively regulate mRNA genes that are involved in many important biological processes and pathways related to development, growth, locomotion, and reproduction as well as response to stresses, particularly oxidative stress. Future efforts will focus on experimental validation of their presence and target mRNA genes to further elucidate their biological functions in earthworms. 相似文献
945.
Copper-catalyzed cross dehydrogenative coupling reactions of tertiary amines with ketones or indoles
A novel cross dehydrogenative coupling (CDC) reaction of N,N-dimethylanilines with methyl ketones by cooperative copper and aminocatalysis has been developed, which leads to the formation of β-arylamino ketones in 42-73% yields. Moreover, the copper-catalyzed alkylation of free (NH) indoles with N,N-dimethylanilines via CDC reaction is also presented, affording alkylated indoles in 52-78% yields. 相似文献
946.
Yongjiang Wu Yunliang Zheng Xuesong Liu Zheng Han Yiping Ren Lishe Gan Changxin Zhou Lianjun Luan 《Journal of separation science》2010,33(8):1072-1078
An ultra‐performance LC in combination with MS/MS method was established to evaluate the quality of Wu‐yao (the dried root of Lindera aggregata (Sims) Kosterm. (Lauraceae)) through simultaneous quantitation of five sesquiterpene lactones, linderagalactone D ( 1 ), linderagalactone C ( 2 ), hydroylindestenolide ( 3 ), neolinderalactone ( 4 ) and linderane ( 5 ). All compounds were separated on a Waters Acquity ultra‐performance LC HSS T3 column (2.1 mm×100 mm, 1.8 μm particle size) with linear gradient elution of acetonitrile and 0.1% formic acid. An ESI interface in the positive mode was employed prior to MS detection. All the compounds showed good linearity (R2≥0.9992). The recoveries, measured at three concentration levels, varied from 97.3 to 103.4% with RSDs <4.8%. The simple, rapid and reliable method was successfully applied to quantify the five components in 13 samples of Wu‐yao from different areas. 相似文献
947.
Qingxiang Zhou Jinli Mao Junping Xiao Guohong Xie 《Journal of separation science》2010,33(9):1288-1293
This paper describes a new method for the direct separation of paraquat and diquat by CZE with ionic liquid 1‐butyl‐3‐methylimidazolium hexafluorophosphate employed as reliable electrolyte. Several factors that affect the separation efficiency were investigated in detail. The experimental results indicated that the optimal running buffer consisted of 50 mM 1‐butyl‐3‐methylimidazolium hexafluorophosphate and 10% ethanol (pH 5.0), applied voltage was 15 kV, and temperature was kept at 30°C and baseline‐separation was achieved within 18 min for the analytes. The proposed method would be very useful and have wide use to monitor the residual level of such pollutants when combined with high‐sensitive detector and an excellent sample preconcentration technique with high enrichment factor in the future. 相似文献
948.
Yuqin Yao Zhihui Cheng Haoyu Ye Yongmei Xie Jing He Minghai Tang Tao Shen Jiangman Wang Yan Zhou Zejun Lu Feng Luo Lijuan Chen Luoting Yu Jin‐Liang Yang Aihua Peng Yuquan Wei 《Journal of separation science》2010,33(9):1331-1337
Ansamitocin P‐3 is a potent anti‐tumor maytansinoid found in Actinosynnema pretiosum. However, due to the complexity of the fermentation broth of Actinomycete, how to effectively separate ansamitocin P‐3 is still a challenge. In this study, both analytical and preparative high‐performance counter‐current chromatography were successfully used to separate and purify ansamitocin P‐3 from fermentation broth. A total of 28.8 mg ansamitocin P‐3 with purity of 98.4% was separated from 160 mg crude sample of fermentation broth in less than 80 min with the two‐phase solvent system of hexane–ethyl acetate–methanol–water (0.6:1:0.6:1, v/v/v/v). The purity and structural identification were determined by HPLC, 1H NMR, 13C NMR and mass spectroscopy. 相似文献
949.
Zheng Han Xuesong Liu Yiping Ren Lianjun Luan Yongjiang Wu 《Journal of separation science》2010,33(13):1923-1932
A speedy and selective ultra‐HPLC‐MS/MS method for simultaneous determination of deoxynivalenol (DON), 3‐acetyldeoxynivalenol (3‐ADON), 15‐ADON, nivalenol and fusarenon X in traditional Chinese medicines (TCMs) was developed. The method was based on one‐step sample cleanup using reliable homemade cleanup cartridges. A linear gradient mobile‐phase system, consisting of water containing 0.2% aqueous ammonia and acetonitrile/methanol (90:10, v/v) at a flow rate of 0.4 mL/min, and an Acquity UPLC HSS T3 column (100 mm×2.1 mm, 1.8 μm) were employed to obtain the best resolution of the target analytes. [13C15]–DON was used as the internal standard to accomplish as accurate as possible quantitation. The established method was further validated by determining the linearity (R2≥0.9990), sensitivity (LOQ, 0.29–0.99 μg/kg), recovery (88.5–119.5%) and precision (RSD≤15.8%). It was shown to be a suitable method for simultaneous determination of DON, 3‐ADON, 15‐ADON, nivalenol and fusarenon X in various TCM matrices. The utility and practical impact of the method was demonstrated using different TCM samples. 相似文献
950.
Yunrui Huang Qingxiang Zhou Junping Xiao Guohong Xie 《Journal of separation science》2010,33(14):2184-2190
This article described a new method for the sensitive determination of organophosphorus pesticides in water samples using SPE in combination with GC‐flame photometric detection. In the procedure of method development, TiO2 nanotubes were used as SPE adsorbents for the enrichment of organophosphorus pesticides from water samples. Several factors, such as eluent and its volume, sample pH, sample volume, sample flow rate, and concentration of humic acid, were optimized. Under the optimal conditions, the proposed method had good linear ranges as 0.1–40 μg/L for each of them, LOD of 0.11, 0.014, and 0.0025 μg/L, and LOQs of 0.37, 0.047, and 0.0083 μg/L for chlorpyrifos, phorate, and methyl parathion, respectively. The proposed method was validated with real environmental water samples and the spiked recoveries were over the range of 86.5–115.1%. All these results indicated that TiO2 nanotubes, as a new SPE adsorbent, would be used widespread for the preconcentraiton and determination of environmental pollutants in the future. 相似文献