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961.
A series of 4-arylidenamino-5-phenyl-4H-1,2,4-triazole-3-thiols have been synthesised and their inclusion complexes have been prepared with β-cyclodextrin. The compounds and their inclusion complexes have been characterised by studying their physical and spectral properties. The thermodynamic stability constant and free energy of activation have been determined to know the stability of inclusion complexes. Finally, the compounds and their inclusion complexes are screened for antibacterial, antioxidant and anthelmintic activities. It is found that inclusion complexes of the newly synthesised compounds have appreciable stability and inclusion complex formation increases the antibacterial, antioxidant and anthelmintic activities significantly as compared to naked compound. 相似文献
962.
963.
V. K. Agrawal S. Karmarkar P. V. Khadikar 《SAR and QSAR in environmental research》2013,24(6):529-545
Abstract The binding of a series of PAT analogues (rodenticides) to the [3H]-mepyramine-labelled H1 receptor in rat and guinea pig brain was investigated topologically using negentropy (N), molecular redundancy (MRI), first-order molecular connectivity (1X v ), Wiener (W), and Szeged (Sz) indices. Multiple regression analyses showed that MRI provided excellent results upon introduction of indicator parameters. Predictive ability of the proposed models was discussed using cross-validation parameters. 相似文献
964.
利用过渡金属盐与3,4,5,6-四氟邻苯二甲酸(TFPT)、1,3-二(4-吡啶基)-丙烷(DPP)和1,4-二(1,2,4-三氮唑)-1-丁烷(BTB)经水热法合成了3个新的配合物:{[M(TFPT)(DPP)]·H2O}n(M=Cd(1),Ni(2)),{[Cd(TFPT)(BTB)0.5]·2H2O}n(3)。通过X射线单晶衍射分析测定了它们的结构。配合物1和2具有相似的一维链结构。中心金属离子表现为扭曲的[MO4N2]八面体构型。配合物3具有二维结构。中心金属离子表现为扭曲的[CdO5N]八面体构型。配合物1和3分别在424 nm、442 nm处出现来自于配体的荧光发射,对应于配体的π*-π的跃迁,配合物2在356 nm处有非常弱的荧光发射。不同金属阳离子对配合物1和3的荧光强度有不同程度的影响,并且通过荧光的猝灭机理,它们都能选择性检测Fe3+离子。 相似文献
965.
The reaction of furan-2,3-diones with S-methylisothiosemicarbazide hydroiodide yielded novel 1,2,4- triazine-5(4H)-ones, and reaction of furan-2,3-diones with diaminomaleonitrile led to the formation of pyrazine-2,3-dicarbonitrile derivatives, and the hydrolysis of these products led to the formation of more new pyrazine-2,3-dicarbonitrile derivatives. These compounds are potential herbicides and pesticides. 相似文献
966.
运用配位场理论方法获得了Ho3+离子低自旋4f95d组态的谱项和J-光谱多重态,根据电偶极跃迁选律合理地解析了LiYF4晶体中Ho3+离子在真空紫外区(120~160 nm)的吸收光谱,4个主要的吸收峰分别被归属为从基态(5I8)到Ho3+离子的低自旋4f95d组态的自旋允许跃迁。 相似文献
967.
以SnCl4和2,4,6-(CF3)3C6H2Li、2,6-(CF3)2C6H3Li为原料合成了两种含大吸电子取代基的化合物Sn[2,4,6-(CF3)3C6H2]2Cl2(缩写为SnAr2Cl2)和Sn[2,6-(CF3)2C6H3]2Cl2(缩写为Sn Ar′2Cl2),利用X射线衍射仪和核磁共振谱仪(19F NMR)表征了产物SnAr2Cl2和SnAr′2Cl2的晶体结构. 相似文献
968.
969.
Fast separations are very desirable in laboratories that analyze large numbers of samples per day or those needing short turn‐around times. Traditional HPLC methods using conventional stationary phases and standard column dimensions require significant amounts of organic solvents and generate large volumes of waste. With growing awareness about the environment, the development of green technologies has been receiving increasing attention. In this work, a very fast green analytical method based on LC‐UV using a short narrow bore column packed with fully porous sub‐2 μm particles has been developed for simultaneous determination of nine pharmaceuticals in wastewater and surface water. The chromatographic separation was optimized in order to achieve short analysis time and good resolution for all analytes in a single run. All analytes could be separated in 1 min with good resolution. Sample preparation was executed by solid phase extraction using Oasis HLB cartridges. The method developed was validated based on parameters such as linearity, precision, accuracy, detection, and quantification limits. The recovery ranged from 70.9 to 92.5% with SDs not higher than 5.4%, except for acetaminophen and sulphanilamide. LODs ranged from 0.6–2.5 μg/L, while the LOQs were in the range 2–8 μg/L. 相似文献
970.
Shuhui Liu Qilong Xie Jiangping Cao Pingping Song Jie Chen Weiwei Bai 《Journal of separation science》2013,36(6):1135-1141
The traditional for the determination of α‐tocopherol in cereal grains includes saponification of a sample followed by liquid–liquid extraction, and it is time‐ and solvent consuming. In this study, a dispersive liquid–liquid microextraction (DLLME) method was developed to extract α‐tocopherol in situ from the saponified grain sample solution. The DLLME experimental parameters including the type and volume of extractants, the volume of dispersers, the addition of salt and the extraction/centrifuging time were examined and optimized. The recommended analytical procedure showed excellent precision (relative SDs of the α‐tocopherol amount of 3.1% over intraday and 7.2% over interday), high sensitivity (the detection limit of 1.9 ng/mL), and strong recovery values (88.9–102.5%). In addition, statistical analyses showed no significant difference between the detected amounts of α‐tocopherol found by the standardized method and this new procedure. The method was successfully applied to determining the amounts and distribution of α‐tocopherol in 14 cereal grain samples. 相似文献