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951.
A series of bridged bis(pyridinylimino) ligands were efficiently synthesized through the condensation reaction of 4,4′-methylene-bis(2,6-disubstituted aniline) with 2-pyridinecarboxaldehyde or 2-benzoylpyridine. They reacted with (DME)NiBr2 to form dinuclear Ni(II) complexes. All resultant compounds were characterized by elemental analysis, IR spectra as well as the single-crystal X-ray diffraction to confirm the structures of ligands and complexes. Activated with methylaluminoxane (MAO), these nickel complexes showed considerably good activities for ethylene oligomerization and polymerization. Their catalytic activities and the properties of PEs obtained were depended on the arched environment of ligand and reaction conditions.  相似文献   
952.
INTRODUCTIONAdsorption has been considered to be the best available technology for removing organics from water in the USSafe Drinking Water Act[1]. Due to many drawbacks of activated carbon[2-7], the most widely used adsorbent,hypercrosslinked polymeric adsorbents developed by Tsyurupa and Davankov[8] have been increasingly viewedas an alternative to activated carbon for selective removal of specific organic substances from contaminatedwater[9-12], and series of researches have been do…  相似文献   
953.
The perfluorohexylated 3,4-ethylenedioxythiophene 5 was prepared via Mitsunobu reaction of perfluorohexylatyed diol 2 with diethyl 3,4-dihydroxythiophenedicarboxylate followed by decarboxylation. The polymerization of 5 was conducted with both oxidative chemical and electrochemical polymerizations. The polymers were characterized by cyclic voltammogram, UV, IR, TGA and DSC.  相似文献   
954.
An intramolecular 1,3-dipolar cycloaddition of azomethine ylide, generated in situ via the reaction of C12-glycinate derivative of macrolide with formaldehyde, provided a novel tricyclic macrolide. The high stereoselectivity of this [2+3] reaction was achieved by introducing a suitable directing group at C-6 position of macrolide.  相似文献   
955.
用等离子体增强化学气相沉积(PECVD)的方法,以固定的氢气(H2)流量和不同的硅烷(SiH4)和甲烷(CH4)流量比沉积了一系列的氢化非晶SiC(a-Si,C1-x-H)膜。用这种宽带隙的a-SixC1-x-H材料作为掺铒的基体材料,通过离子注入的方法得到掺铒的a-SixC1-x-H(a-SixC1-x-H:Er)膜。注入以后的样品经过不同温度的退火。用X射线光电子能谱(XPS)、红外吸收光谱(IR)、拉曼散射谱(Raman)等技术研究不同的SiH4/CH4流量比和退火温度对a-SixC1-x-H:Er发光强度的影响。结果表明,高温退火引起了膜中C的分凝,对饵的发光是不利的。通过低温和室温下铒发光强度的比较,表明这种材料具有较弱的温度猝灭效应。  相似文献   
956.
New spirocyclic heterocycles 8, 16, 19/20, 25, 27 , and 30 derived from pyrimido[4,5‐b][1,4]diazepin]‐8′(9′H)‐one were synthesised by a tandem nitroso‐ene/Diels–Alder reaction of 4‐(alkenoylamino)‐5‐nitrosopyrimides. The crystal structure of 16 was established by X‐ray analysis. It is characterised by four pairs of intermolecular H‐bonds linking every two molecules in the unit cell. Sequential imine reduction and intramolecular condensation of the C(4′)‐(acylamino)‐pyrimido[4,5‐b][1,4]diazepines 27 and 30 led to the [1,4]diazepino[1,2,3‐gh]purines 28 / 29 and 31 , respectively.  相似文献   
957.
The polypnictide complexes of rare earth cations have drawn the attention of the scientific community for their uncommon bonding modes and potential applications. Herein, we present a systematic and comprehensive summary on recent advances in the field of rare earth polypnictides, focusing on their synthesis, structures, and reactivities. The structural stabilizing effects imposed by the electropositive rare earth cations as well as the reducing capability of rare earth precursors in the synthesis of these polypnictide complexes are described in this review. We also disscuss in detail the bonding interactions and coordination modes between rare earth cations and polypnictide clusters as well as the similarities and the peculiarity of some structures.  相似文献   
958.
In the study, we developed a simple, rapid, sensitive, and inexpensive method for determination of the disease biomarkers of acetone, hexanal and heptanal in human blood. For the first time, derivatization of carbonyls with O-2,3,4,5,6-(pentafluorobenzyl)hydroxylamine (PFBHA) was combined with headspace single-drop microextractin (HS-SDME) and gas chromatography-mass spectrometry (GC–MS) and applied to the analysis of acetone, hexanal, and heptanal in human blood. At first, acetone, hexanal and heptanal in blood were derivatized with PFBHA and formed oximes in several seconds. Sequentially, the oximes were headspace extracted and concentrated by a microdrop solvent. Finally, the extracted oximes were analyzed by GC–MS. HS-SDME conditions and method validations were studied. Due to needing of only 2 μl organic solvent, short extraction time of 8 min, and simple operation, derivatization-HS-SDME was shown to be a rapid, simple, and inexpensive technique for analysis of acetone, hexanal, and heptanal in human blood. Moreover, it had low detection limit values from 0.24 to 0.62 nM, and good reproducibility (R.S.D. less than 12%).  相似文献   
959.
紫外分光光度法测定甲砜霉素片的含量   总被引:4,自引:0,他引:4  
根据甲砜霉素的紫外吸收特征,建立了以乙腈-水为溶媒、(225±1)nm为最大吸收波长的紫外分光光度法。方法的线性范围为0.5~25.0μg/mL,平均回收率为99.92%,RSD为0.30%。用对照品比较法测定5批甲砜霉素片的含量,并与中国药典方法的测定结果进行比对,结果表明,两种方法的测定结果基本一致。  相似文献   
960.
In GaAs based infrared detectors, a considerable part of the incident light will be reflected at the surface, thus it decreases the detectors sensitivity considerably. In this paper, a TiO2 nanoporous coating was prepared successfully on the GaAs substrate by sol-gel method. The optical parameters of the coating were also controlled successfully. It was proved that the coating could greatly improve the transmittance of the incident light, which agrees with the theoretical results quite well. In the 2.5–6.0 m waveband, the maximum transmittance of GaAs substrate is 56%, while the transmittance of the GaAs substrate coated with a nanostructured TiO2 coating is about 94%.  相似文献   
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