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181.
182.
Polycapillary X-ray optics (capillary X-ray lens) are now popular in X-ray fluorescence (XRF) analysis. Such an X-ray lens can collect X-rays emitted from an X-ray source in a large solid angle and form a very intense X-ray microbeam which is very convenient for microbeam X-ray fluorescence (MXRF) analysis giving low minimum detection limits (MDLs) in energy dispersive X-ray fluorescence (EDXRF). A new method called position sensitive X-ray spectrometry (PSXS) which combines an X-ray lens used to form an intense XRF source and a position sensitive detector (PSD) used for wavelength dispersive spectrometry (WDS) measurement was developed recently in the X-ray Optics Laboratory of Institute of Low Energy Nuclear Physics (ILENP) at Beijing Normal University. Such a method can give high energy and spacial resolution and high detection efficiency simultaneously. A short view of development of both the EDXRF using a capillary X-ray lens and the new PSXS is given in this paper. 相似文献
183.
Yu Mao Wenxuan Zhao Shuo Lu Lei Yu Yi Wang Yong Liang Shengyang Ni Yi Pan 《Chemical science》2020,11(19):4939
Redox-active esters (RAEs) as alkyl radical precursors have demonstrated great advantages for C–C bond formation. A decarboxylative cross-coupling method is described to afford substituted alkynes from various carboxylic acids using copper catalysts CuCl and Cu(acac)2. The photoexcitation of copper acetylides with electron-rich NEt3 as a ligand provides a general strategy to generate a range of alkyl radicals from RAEs of carboxylic acids, which can be readily coupled with a variety of aromatic alkynes. The scope of this cross-coupling reaction can be further expanded to aliphatic alkynes and alkynyl silanes using a catalytic amount of preformed copper-phenylacetylide. In addition, DFT calculations revealed the favorable reaction pathway and that the bidentate acetylacetonate ligand of the copper intermediate plays an important role in inhibiting the homo-coupling of the alkyne.Redox-active esters (RAEs) as alkyl radical precursors have demonstrated great advantages for Cu-catalysed C–C bond formation. 相似文献
184.
185.
Xu W. B. Zhou Z. F. He P. S. Pan W.-P. 《Journal of Thermal Analysis and Calorimetry》2004,78(1):113-124
The Flory's gelation theory, non-equilibrium thermodynamic fluctuation theory and Avrami equation have been used to predict
the gel time t
g and the cure behavior of epoxy resin/organo-montmorillonite/diethylenetriamine intercalated nanocomposites at various temperatures
and organo-montmorillonite loadings. The theoretical prediction is in good agreement with the experimental results obtained
by dynamic torsional vibration method, and the results show that the addition of organo-montmorillonite reduces the gelation
time t
gand increases the rate of curing reaction, the value of k, and half-time of cure after gelation point t1/2 decreases with the increasing of cure temperature, and the value of n is ~2 at the lower temperatures (<60°C) and decreases to ~1.5 as the temperature increases, and the addition of organo-montmorillonite
decreases the apparent activation energy of the cure reaction before gelation point, but has no apparent effect on the apparent
activation energy of the cure reaction after gelation point. There is no special curing process required for the formation
of epoxy resin/organo-montmorillonite/diethylenetriamine intercalated nanocomposite.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
186.
以D-核糖为原料,合成了1,4-脱水一双(氧特丁基二甲基甲硅烷基)-α-D-吡喃核糖(ADSR)和1,4-脱水-2,3-氧-亚异丙基-α-D-吡喃核糖(AIRP),研究了它们在SbCl5催化下的开环共聚合反应,并测定了共聚产物的比旋光度、分子量及1H、13CNMR谱。结果表明,尽管AIRP在均聚中总是得到单一的1-4β结构产物,而在共聚产物中,AIRP结构单元则为1—4β和1-5α的混合结构。同时发现,聚合温度对共聚物的产率和立体结构均有较大的影响。 相似文献
187.
Wen‐Bin Pan Li‐Mei Wei Li‐Lan Wei Chin‐Chung Wu Fang‐Rong Chang Yang‐Chang Wu 《中国化学会会志》2005,52(3):581-588
Oxidation of a series of phenols with cerium(IV) ammonium nitrate (CAN) in acetonitrile under mild conditions yields the mixture of corresponding nitrophenols. In the cases of methylphenols and hydroxy ‐carboxylic acids, the steric effect may reduce the nitration reaction. Compounds 3a and 4b showed selective activities to Hep 3B and Hep G2 cancer cell lines, respectively. Compound 2c showed selective activities to Hep G2 and MDA‐MB‐231 cancer cell lines. Furthermore, compound 10b showed selective activities to Hep G2, Hep 3B, MCF‐7 and MDA‐MB‐231 cancer cell lines. 相似文献
188.
The triblock copolymers, poly(styrene-b-isoprene-b-ε-caprolactone)s (PS-b-PI-b-PCL) have been synthesized successfully by combination of anionic polymerization and ring-opening polymerization. Diblock copolymer capped with hydroxyl group, PS-b-PI-OH was synthesized by sequential anionic polymerization of styrene and isoprene and following end-capping reaction of EO, and then it was used as macro initiator in the ring-opening polymerization of CL. The results of DSC and WAXD show big effect of amorphous PS-b-PI on the thermal behaviors of PCL block in the triblock copolymers and the lower degree of crystalline in the triblock copolymer with higher molecular weight of PS-b-PI was observed. The real-time observation on the polarized optical microscopy shows the spherulite growth rates of PCL27, PCL328 and PS-b-PI-b-PCL344 are 0.71, 0.46 and 0.07 μm s−1, respectively. The atomic force microscopy (AFM) images of the PS90-b-PI66-b-PCL28 show the columns morphology formed by it’s self-assembling. 相似文献
189.
Yi‐Zhen Tang Hao Sun Ya‐Ru Pan Xiu‐Mei Pan Rong‐Shun Wang 《International journal of quantum chemistry》2007,107(6):1495-1501
The mechanisms for the reaction of CH3S with NO2 are investigated at the QCISD(T)/6‐311++G(d,p)//B3LYP/6‐311++G(d,p) on both single and triple potential energy surfaces (PESs). The geometries, vibrational frequencies, and zero‐point energy (ZPE) correction of all stationary points involved in the title reaction are calculated at the B3LYP/6‐311++G(d,p) level. More accurate energies are obtained at the QCISD(T)/6‐311++G(d,p). The results show that 5 intermediates and 14 transition states are found. The reaction is more predominant on the single PES, while it is negligible on the triple PES. Without any barrier height for the whole process, the main channel of the reaction is to form CH3SONO and then dissociate to CH3SO+NO. © 2006 Wiley Periodicals, Inc. Int J Quantum Chem, 2007 相似文献
190.
Yan-Ping Liu Li-Li Sun Xiang-Lin Zhang Hai-Yuan Niu Zheng-Hong Pan 《Natural product research》2020,34(16):2295-2300
Abstract A phytochemical investigation on the stems of Mappianthus iodoides led to the isolation of a new naturally occurring prenylated isoflavone, mappianthone A (1), together with seven known analogues (2?8). The structure of 1 was elucidated by extensive spectroscopic methods and the known compounds were identified by comparison with data reported in the literature. All isolated compounds were evaluated for their antiproliferative activities against five human cancer cell lines: HL-60, SMMC-7721, A-549, MCF-7 and SW480 in vitro. Compounds 1?8 showed significant antiproliferative effects against several human cancer cell lines with IC50 values ranging from 0.16 to 12.68?μM. 相似文献