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951.
952.
Diffusion of monatomic guest species within confined media has been understood to a good degree due to investigations carried
out during the past decade and a half. Most guest species that are of industrial relevance are actually polyatomics such as,
for example, hydrocarbons in zeolites. We attempt to investigate the influence of non-spherical nature of guest species on
diffusion. Recent molecular dynamics (MD) simulations of motion of methane in NaCaA and NaY, benzene in NaY and one-dimensional
channels AlPO4−5, VPI−5 and carbon nanotube indicate interesting insights into the influence of the host on rotational degrees of freedom
and orientational properties. It is shown that benzene in one-dimensional channels where the levitation parameter is near
unity exhibits translational motion opposite to what is expected on the basis of molecular anisotropy. Rotational motion of
benzene also possesses rotational diffusivities aroundC
6
and C2axes opposite to what is expected on the basis of molecular geometry. Methane shows orientational preference for 2+ 2 or 1
+ 3 depending on the magnitude of the levitation parameter. 相似文献
953.
We design a novel X-ray image detector by lens coupling a Gd2O2S:Tb intensifying screen with a high performance low-light-level (L3,which often means luminescence less than 10-3 Lux) image intensifier.Different coupling effects on imaging performance between zoom lens and fix-focus lens are analyzed theoretically.In experiment,for designing a detector of 15-inch visual field,the system coupled by zoom lens is of 12.25-1p/cm resolution,while the one with fix-focus lens is 10 lp/cm.The superiority of zoom lens is validated.It is concluded that zoom lens preserves the image information better than fix-focus lens and improves the imaging system's performance in this design,which is referential to the design of other optical imaging systems. 相似文献
954.
Ravi Shankar Vandana Shahi 《Journal of polymer science. Part A, Polymer chemistry》2008,46(23):7816-7826
The polysilanes [RMe2Si(CH2)x(Me)Si]n [x = 2, 3; R = 2‐Fu ( 1, 2 ), 5‐Me‐2‐Fu ( 3, 4 )] bearing furyl‐substituted carbosilyl side chains have been synthesized by dehalocondensation reaction (Wurtz coupling) of the corresponding carbosilanes using sodium dispersion in refluxing toluene. On the other hand, analogous polysilanes with appended thienyl groups [x = 2, 3; R = 2‐Th ( 5, 6 ), 4‐Me‐2‐Th ( 7, 8 )] are only accessible by the reaction of the corresponding carbosilane precursors under mild Wurtz coupling conditions (THF, RT). These polysilanes reveal monomodal molecular weight distribution with Mw/PDI = 3.3–5.4 × 104/1.22–1.47 ( 1–4 ) and 9.1–14.4 × 104/1.45–1.61 ( 5–8 ) and are characterized by FT‐IR, multinuclear (1H, 13C{1H}, 29Si{1H}) NMR, and UV/PL spectral studies as well as thermogravimetric analysis (TGA). Preliminary studies on the reactivity of polysilane 2 with palladium acetate (toluene, RT) reveal the formation of spherical palladium nanoparticles of size 8.2 ± 0.6 nm, which remain stable in solution for several weeks. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 7816–7826, 2008 相似文献
955.
956.
Hongliang Guan 《Talanta》2009,79(2):153-1486
In this contribution, we designed a fluorescent thiophene copolymer to detect insertion/deletion mutation in DNA by doping aldehyde group in the main chain. The fluorescence of the copolymer could be dramatically quenched on the addition of single-stranded DNA (ssDNA) via strong electrostatic interactions and electronic/energy transfer. Although the complementary ssDNA made the fluorescence recover, the hydrogen bonds and chemical coupling also played a significant role between the unpaired bases and aldehyde group, which could differentiate the subtle differences in such mutant DNA. The influence of buffer pH, concentration of NaCl, heating time and the temperature was systemically investigated and the proposed method was then successfully applied to detect real sample. With the respect to the linearity, limit of detection precision, specificity, this procedure could provide sensitive methodologies for the rapid detection and identification of nucleic acids. 相似文献
957.
The difference between the full revolution adiabatic-to-diabatic transformation angle, or the loop-integrated nonadiabatic coupling term, and the Berry phase is calculated perturbationally, when one or more excited states are coupled into a ground doublet. The difference is in general non-zero, but has no definite sign. A molecule distorted from a Renner–Teller situation serves as an illustration. 相似文献
958.
The Suzuki cross‐coupling reaction of various bromine‐containing substrates and phenylboronic acid in toluene at 90 °C on a Pd(AcO)2Py2 catalyst supported on an Mg? Al hydrotalcite, using K2CO3 as the base, was studied. The conversion and selectivity results obtained for many of the substrates were excellent and similar to those provided by more active or even homogeneous catalysts. The reactions of aryl polybromides and phenylboronic acid gave the corresponding polyaromatic compounds in variable yields depending on the particular substrate. Arylation occurred in a consecutive manner by substitution of the different Br atoms. ICP‐MS measurements of the palladium content of the catalyst performed prior to and after the reaction revealed that part of the metal is incorporated into the bulk solution; therefore, the catalytic process is not purely heterogeneous. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
959.
Qiang Fu Chao Liu Wencheng Lin Junlian Huang 《Journal of polymer science. Part A, Polymer chemistry》2008,46(20):6770-6779
Heterograft copolymers poly(4‐glycidyloxy‐2,2,6,6‐tetramethylpiperidine‐1‐oxyl‐co‐ ethylene oxide)‐graft‐polystyrene and poly(tert‐butyl acrylate) (poly (GTEMPO‐co‐EO)‐g‐PS/PtBA) were synthesized in one‐pot by atom transfer nitroxide radical coupling (ATNRC) reaction via “graft onto.” The main chain was prepared by the anionic ring‐opening copolymerization of ethylene oxide (EO) and 4‐glycidyloxy‐2,2,6,6‐tetramethylpiperidine‐1‐oxyl (GTEMPO) first, then the polystyrene and poly (tert‐butyl acrylate) with bromine end (PS‐Br, PtBA‐Br) were prepared by atom transfer radical polymerization (ATRP). When three of them were mixed each other in the presence of CuBr/N,N,N′,N″,N″‐pentamethyldiethylenetriamine (PMDETA) at 90 °C, the formed secondary carbon radicals at the PS and PtBA chain ends were quickly trapped by nitroxide radicals on poly(GTEMPO‐co‐EO). The heterograft copolymers were well defined by 1H NMR, size exclusion chromatography, fourier transform infrared, and differential scanning calorimetry in detail. It was found that the density of GTEMPO groups on main chain poly(GTEMPO‐co‐EO), the molecular weights of PS/PtBA side chains, and the structure of macroradicals can exert the great effects on the graft efficiency. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 6770–6779, 2008 相似文献
960.
在高斯光束传输理论的基础上,利用矩阵光学原理和高斯光束耦合理论,得出光学相干层析系统中参考反射镜的空间位置对系统耦合效率影响的表达式,并用计算机模拟系统的耦合效率与参考反射镜和棒透镜间的距离及参考反射镜偏转角度的关系曲线。实验结果和理论分析相符合。 相似文献