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51.
One new lactone, cyclopentanepyrone A ( 1 ), and two new monoterpenoids, gardeterpenone A ( 2 ) and jasminoside V ( 3 ), were isolated from the fruits of Gardenia jasminoides var. radicans, along with four known monoterpenoids, 4 – 7 , which were isolated from this plant for the first time. The structures of the isolates were elucidated by extensive spectroscopic studies, including UV, IR, 1D‐ and 2D‐NMR, ESI‐MS, HR‐ESI‐MS, and CD experiments.  相似文献   
52.
Yu  Ningxiang  Peng  Hailong  Xiong  Hua  Wu  Xiaqing  Wang  Xiaoyan  Li  Yanbin  Chen  Lingxin 《Mikrochimica acta》2015,182(13):2139-2146

A fluorescent probe for the sensitive and selective determination of sulfide ions is presented. It is based on the use of graphene quantum dots (GQDs) which emit strong and stable blue fluorescence even at high ionic strength. Copper(II) ions cause aggregation of the GQDs and thereby quench fluorescence. The GQDs-Cu(II) aggregates can be dissociated by adding sulfide ions, and this results in fluorescence turn on. The change of fluorescence intensity is proportional to the concentration of sulfide ions. Under optimal conditions, the increase in fluorescence intensity on addition of sulfide ions is linearly related (r 2 = 0.9943) to the concentration of sulfide ions in the range from 0.20 to 20 μM, and the limit of detection is 0.10 μM (at 3 σ/s). The fluorescent probe is highly selective for sulfide ions over some potentially interfering ions. The method was successfully applied to the determination of sulfide ions in real water samples and gave recoveries between 103.0 and 113.0 %.

Graphene quantum dots (GQDs) emit strong blue fluorescence which, however, is quenched by copper(II) ions due to the formation of GQDs-Cu(II) aggregates. Fluorescence is recovered by sulfide ions due to the dissociation of GQDs-Cu(II) aggregates.

  相似文献   
53.
在低共熔溶剂氯化胆碱/草酸催化作用下,由醛、吲哚和6,10-二氧杂螺[4.5]十烷-7,9-二酮三组分多米诺Knoevenagel-Michael反应合成了一系列新型螺环吲哚衍生物,产率为70%~97%.该方法条件温和,操作简单,反应时间短,对环境友好等优点,且催化剂廉价易得.  相似文献   
54.
A new benzamide (1) and four known compounds (25) were isolated from endophytic Streptomyces YIM67086, and their structures were determined as 2-amino-3,4-dihydroxy-5-methoxybenzamide (1), 4-hydroxy-3-methoxybenzoic acid (2), phenylacetic acid (3), N-acetyltyramine (4) and p-hydroxytruxinic acid (5). Compound 5 was first found in the microorganism. The antimicrobial activities of compounds 15 and antioxidant activity of compound 1 were investigated.  相似文献   
55.
A simple and rapid method was established and validated for the simultaneous quantification of 10 saponins, namely ginsenosides-Rb1, Rb2, Rb3, Rc, Rd, Rg1, Rg2, Re, Rf and Notoginsenside R1, in Chinese Shizhu Panax by ultra performance liquid chromatography coupled with an electrospray mass spectrometry (UPLC-ESI-MS). In addition, the contents of the analytes in different parts of Chinese Shizhu Panax were also analysed. The results showed that the concentration of saponins had a reference to the different parts of Chinese Shizhu Panax. The established method could be used as a new analytical approach for assessment of the quantity of Chinese Shizhu Panax.  相似文献   
56.
A novel method for the screening of 151 drugs of abuse and toxic compounds in human whole blood has been developed and validated by online solid‐phase extraction with liquid chromatography coupled to time‐of‐flight mass spectrometry. Analytes were extracted and separated by using a fully automated online solid‐phase extraction liquid chromatography system with total chromatographic run time of 26 min. Time‐of‐flight mass spectrometry screening of 151 drugs of abuse and toxic compounds was performed in a full‐scan (m/z 50–800) mode using an MSE acquisition of molecular ions and fragment ions data at two collision energies (one was 6 eV and another one was in the range of 5–45 eV). The compounds were identified based on retention times and exact mass of molecular ions and fragment ions. The limit of detection ranged from 1 to 100 ng/mL and the recovery of the method ranged from 6.3 to 163.5%. This method is proved to be a valuable screening method allowing fast and specific identification of drugs in human whole blood.  相似文献   
57.
We successfully synthesized the first hemin-montmorillonite bio-conjugate with an amino acid residue to mimic natural peroxidase enzyme. Histamine was intercalated in montmorillonite by cation exchange, then a hemin molecule was loaded onto the histamine-montmorillonite with an adsorption capacity of 7.0 mg g-1. The hemin-histamine-montmorillonite conjugate shows high peroxidase activity as indicated by the oxidation of guaiacol, which is attributed to the activation of hemin by Fe–N complex formation between the imidazole group in histamine and the iron ion in the hemin molecule. Temperature- dependent peroxidase activity for this synthesized biomimetic material indicates that raising the reaction temperature could significantly enhance the activity of the conjugate. The biomimetic catalyst has good reusability; nearly 100% activity can be retained after three cycles. Because montmorillonite clay is widely distributed in the environment, this material offers great potential for in situ and ex situ remediation of many organic contaminants in surface/subsurface soils.  相似文献   
58.
59.
建立电感耦合等离子体原子发射光谱标准加入法测定铜精矿中Zn、Pb、As、Cu、Bi、MgO.分别对酸的加入种类和数量进行条件试验,采用盐酸–硝酸–盐酸–氢氟酸–高氯酸溶样,以标准加入法配制系列标准工作溶液,建立校正曲线,有效消除了样品基体对目标物检测结果的影响.目标物的分析谱线分别为Zn 206.2 nm,Pb 182.2 nm,As 197.2 nm,Cu 324.7 nm,Bi 190.2 nm,MgO 279.5 nm.各目标物校正曲线线性相关系数均不小于0.999,检出限为0.0002%~0.0006%,测定结果的相对标准偏差为0.62%~8.92%(n=6).按照该方法测定ZBK337、ZBK340铜精矿标准物质中Zn、Pb、As、Cu、Bi、MgO,测定值均在规定的标准值再现性限范围内.  相似文献   
60.
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