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991.
A series of metal–organic frameworks built from a propionate-functionalized purine-containing ligand 3-(6-oxo-6,9-dihydro-1H-purin-1-yl)propanoic acid (H2L), {[La(HL)3(H2O)2]·2H2O}n (1), {[Ce(HL)3(H2O)2]·4H2O}n (2), [Co(HL)2(H2O)2]n (3), {[Cd(L)(H2O)]·0.5H2O}n (4) and {[Pb(HL)(C2O4)0.5(H2O)]·2H2O}n (5), was synthesized and characterized. Isostructural 1 and 2 have polymeric chain structures further linked into 3-D porous supramolecular frameworks with 1-D open channels through complicated interchain hydrogen bonding interactions. At 77 K and 1 bar, the dehydrated porous materials 1 and 2 show adsorption behaviors with maximum nitrogen uptakes of 14 and 23 mL g?1, respectively. Complexes 35 are 2-D coordination polymers but have different topological structures. Metallohelicate 3 has (4,4) nets composed of left- and right-handed metal–organic helices sharing the common metal centers, but metallohelicate 4 possesses (4·82) topology and 5 has 63-topological structure. In 3 and 5, the polymeric layers are further assembled through regular interlayer hydrogen bonding interactions to form 3-D supramolecular frameworks. Additionally, the thermostabilities of 15 as well as the magnetism of 3 were also investigated.  相似文献   
992.
A graphene monolithic column was fabricated in a capillary using π-electron-rich poly(N-vinylcarbazole-divinylbenzene) as the supporter through in situ one-step polymerization for the enrichment of trace benzodiazepines in biological samples. This new three-dimensional monolith showed uniformity and a continuous column bed; more importantly, it retained the unique properties of graphene that are typically associated with individual graphene sheets. Based on the large delocalized π-electron system, graphene forms ππ stacking interactions with benzodiazepines and benzene rings of poly(N-vinylcarbazole-divinylbenzene), which not only enhance the extraction performance for benzodiazepines compared to the neat polymer but also provide chemical stability of the graphene monolith. Moreover, several factors likely to affect the extraction, including ionic strength, sample pH, sample volume, and eluant volume were studied in detail. The optimized method gave a linear range of 0.005–1?ng?mL?1, and detection limits of 1.12–2.35?ng?L?1. Finally, the graphene monolith was successfully applied to the separation and enrichment of benzodiazepines from urine and hair samples coupled with high-performance liquid chromatography–mass spectrometry. The recoveries were in the range of 78.6–85.6% for urine and 87.2–94.3% for hair with relative standard deviations of 3.4–6.9 and 2.9–8.3%, respectively.  相似文献   
993.
Mass spectrometry (MS)-based proteome profiling is essential for molecular diagnostics in modern biomedical study. To date, sample preparation including protein extraction and proteolysis is still very challenging and lack of efficiency. Recently tips-based sample preparation protocols exhibit strong potentials to achieve the goal of “a proteome in an hour”. However, in-tip proteolysis is still rarely reported and far from ideal for dealing with complex bio-samples. In this work, nanoreactors encapsulated micropipette tips were demonstrated as high performance devices for fast (∼minutes) and multiplexing proteolysis to assist the profiling of cancer cells proteome. Nanoporous silica materials with controlled pore size and surface chemistry were prepared as nanoreactors and encapsulated in micropipette tips for efficient in situ proteolysis. The as-constructed device showed desirable sensitivity (LOD of 0.204 ± 0.008 ng/μL and LOQ of 0.937 ± 0.055 ng/μL), selectivity, stability (two months under −20 °C), reusability (at least 10 times), and little memory effect in MS based bottom-up proteomic analysis. It was used for comprehensive protein mapping from cancer cell lines. The number of identified proteins was increased by 18%, 22%, 52%, and 52% dealing with HepG2, F56, MCF7, and HCCLM3 cancer cells, compared to traditional in-solution proteolysis based bottom-up proteomic strategy. With the enhanced performance, our work built a novel, efficient and miniaturized platform for facile proteomic sample preparation, which is promising for advanced biomarkers discovery in biomedical study.  相似文献   
994.
A metal-free oxidative arene/alkene annulation-aromatization has been realized, which enables efficient synthesis of 2-arylnaphtho[2,1-b]furans from readily available terminal aryl alkenes and 2-naphthols. Mechanistic study suggests that this reaction proceeds via free-radical initiated tandem cyclization, dehydrogenative rearomatization and aromatization.  相似文献   
995.
An efficient double Michael addition of nitromethane to divinyl ketones was established in good to high yields (75–99%). A wide range of cyclohexanones were obtained with excellent diastereocontrol (up to >20:1 dr) and enantioinduction (91–99% ee) in a one-pot fashion. The involvement of basic additive significantly enhanced the reactivity of this cascade sequence.  相似文献   
996.
The formation of microemulsions in the presence of cyclohexane, Triton X-100, n-butanol, water, and task-special ionic liquid (TSIL) (1-2-aminoethyl-3-butylimidazolium tetrafluoroborate) was studied at 25°C. The phase behavior of this ternary system was investigated. Three subregions (namely, water-in-oil phase, bicontinuous phase, and oil-in-water phase) were identified in the single-phase region by dynamic light scattering (DLS) technique and electrical conductivity measurement. Microstructures of microemulsions with different water contents have been predicted by using dissipative particle dynamics (DPD) simulation. It was found that the DPD simulations successfully reproduce the experimental results in the article. The location of TSIL in the microemulsions was predicted by DPD simulation further. The result indicates that TSIL is more easy to locate in the surfactant and cosurfactant layer and has amphiphilicity, which provides us new insights into the potential applications of TSIL-based microemulsions in separation and new nano-scale material preparation because of the interaction of TSIL with some special components at the interface of oil and water.  相似文献   
997.

An integrated automation system of routine instrumental neutron activation analysis (INAA) with three HPGe detectors has been built at China Institute of Atomic Energy. This system is mainly composed of sample counting system, pneumatic transfer system, software control and analysis systems, etc. The characteristics include more than 200 samples can be controlled for a batch of INAA with three detectors simultaneously, sample counting position can be optimized automatically according to the counting dead time, the real-time tracking and the high consistency between the spectrum and counting sample are possible to be realized through radio frequency identification tag.

  相似文献   
998.
In this work,the effect of dioctadecyl dimethyl ammonium chloride(DDAC,a kind of alkyl ammonium salt) on polar β phase content and the diameter of electrospun PVDF nanofibers was investigated for the first time.Our experimental results show that the diameter of the electrospun PVDF nanofiber could be largely reduced and the content of polar β phase also become dominant immediately by just adding a little amount of DDAC.When the mass fraction of DDAC reached 4%,the content of polar β phase increased by about 39.1% compared with PVDF nanofibers without DDAC.Besides,the crystallinity of PVDF nanofibers also increased with the addition of DDAC.Based on the results,the possible mechanism of cooperative effect between electrospinning and DDAC on fiber diameter and formation of β phase in PVDF was discussed.  相似文献   
999.
Here, we compared the conversion of gasoline-ranged n-alkanes (C6–C9) using dielectric barrier discharge. For an energy density of ~68 J/L and an initial n-alkane concentration of ~230 ppm, when carbon number increased from 6 to 9, the energy efficiency of n-alkane conversion increased from 117 to 240 mmol/kWh, CO x selectivity decreased from 46 to 20%, and ozone concentration increased from 216 to 240 ppm. The effect of energy density and initial n-alkane concentration were also investigated. The understanding of initial step of conversion was greatly aided by a proposed kinetic model. The pathways of consecutive reactions from the initiation to products were also discussed.  相似文献   
1000.
三峡工程坝址花岗岩体缓倾角结构面成因综合研究   总被引:1,自引:0,他引:1  
本文对长江三峡工程坝址花岗岩体中缓倾角结构面成因进行了全面的综合研究。从野外地质调查人手,在大量野外勘测的基础上进行宏观分析,同时辅之以扫描电镜、透射电镜、包体温度测定等方法进行微观构造组构、差异应力等的研究。在地质力学宏观分析的基础上,利用地质力学物理模拟进行相似条件下的反演,并利用非线性有限元数值模拟进行验证。同类研究在国内外均未见先例,可为同类工程研究借鉴。  相似文献   
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