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21.
The feasibility of alignment control of low-molecular-weight guest species by controlling the orientation of mesochannels in a mesoporous silica host has been shown for the first time; spectroscopically anisotropic absorption behaviour of a cyanine dye was observed upon its incorporation into the mesochannels of a mesoporous silica film with uniaxially aligned porous structure, proving that the preferred alignment of the dye molecules was achieved on a macroscopic scale. 相似文献
22.
Alexei N. Grum-Grzhimailo Tatiana Pikuz Anatoly Faenov Takeshi Matsuoka Norimasa Ozaki Bruno Albertazzi Sergei Pikuz Yuichi Inubushi Makina Yabashi Kensuke Tono Hirokatsu Yumoto Haruhiko Ohashi Tetsuya Ishikawa Ryosuke Kodama 《The European Physical Journal D - Atomic, Molecular, Optical and Plasma Physics》2017,71(3):69
23.
An equation of state based on the Weeks-Chandler-Andersen (WCA) perturbation theory utilizing the simplified random-phase approximation (RPA) term is p of state is applied successfully to calculate the P-V-T relationship for a spherical molecule, argon.For nonspherical molecules, the effects of anisotropic interactions are treated empirically. The calculated P-V-T relationships and saturated properties for nonspherical and nonpolar molecules agree well with experimental data. The potential parameters for nonpolar substances are well correlated with the acentric factors. 相似文献
24.
Jun-ichi Yoshida Katsuhiko Muraki Hirokatsu Funahashi Nariyoshi Kawabata 《Journal of organometallic chemistry》1985,284(2):C33-C35
Electrochemical reduction of allyl, vinyl, and aryl halides in the presence of a silylating agent (Me3SiCl, HMe2SiCl, or PhMe2SiCl) afforded the corresponding organosilicon compounds offering a valuable method for introduction of a silyl group into organic molecules. 相似文献
25.
Hirokatsu Yumoto Takahisa Koyama Satoshi Matsuyama Yoshiki Kohmura Kazuto Yamauchi Tetsuya Ishikawa 《Synchrotron Radiation News》2016,29(4):27-31
Ellipsoidal mirror optics can produce a smaller, two-dimensional focus with diffraction-limited properties than is possible when using mirror optics in Kirkpatrick–Baez (K–B) geometry [1]. This is because ellipsoidal focusing mirrors can be designed such that they have a larger numerical aperture in the sagittal focusing direction as compared to that in the meridional focusing direction. Although ellipsoidal focusing mirrors have this crucial advantage over K–B optics, K–B optics are widely utilized as micro-/nano-focusing devices [2–8] in synchrotron radiation facilities and X-ray free electron laser facilities [9, 10]. Figure 1 shows a schematic of focusing mirror optics; Figure 1(a) shows the ellipsoidal mirror and Figure 1(b) the K–B mirror arrangement. In K–B geometry, two mirrors with a one-dimensionally curved surface, such as an elliptical cylinder, are orthogonally arranged in tandem to reflect and focus light independently in a direction perpendicular to each other under grazing-incidence conditions. Ellipsoidal focusing mirrors, which can generate a two-dimensional focusing beam by a single reflection, have a highly sloped surface with a two-dimensional aspherical shape, when compared to elliptical-cylinder mirrors that are used for line-focusing in K–B geometry. In addition, surface shapes of nano-focusing mirrors must be fabricated with nanometer-level accuracy. Therefore, fabrication of ellipsoidal nano-focusing mirrors is extremely difficult. There are no reports on ellipsoidal nano-focusing mirrors in the hard X-ray region with superior performances to provide diffraction-limited beams. 相似文献
26.
Simultaneous determination of inorganic mercury and methylmercury compounds in natural waters 总被引:3,自引:0,他引:3
The purpose of the present work was to develop a simple, rapid, sensitive and accurate method for the simultaneous determination of inorganic mercury (Hg(2+)) and monomethylmercury compounds (MeHg) in natural water samples at the pg L(-1) level. The method is based on the simultaneous extraction of MeHg and Hg(2+)dithizonates into an organic solvent (toluene) after acidification of about 300 mL of a water sample, followed by back extraction into an aqueous solution of Na(2)S, removal of H(2)S by purging with N(2), subsequent ethylation with sodium tetraethylborate, room temperature precollection on Tenax, isothermal gas chromatographic separation (GC), pyrolysis and cold vapour atomic fluorescence spectrometric detection (CV AFS) of mercury. The limit of detection calculated on the basis of three times the standard deviation of the blank was about 0.006 ng L(-1) for MeHg and 0.06 ng L(-1) for Hg(2+)when 300 mL of water was analysed. The repeatability of the results was about 5% for MeHg and 10% for Hg(2+). Recoveries were 90-110% for both species. 相似文献
27.
Fluorine-containing esters were demonstrated to be convenient substrates for construction of the corresponding ketones by low temperature reaction with Grignard reagents followed by warming up to 0 °C, while heating the mixture up to 80 °C readily promoted the reduction of the ketones obtained by the generated magnesium alkoxides whose mechanism was speculated as Meerwein-Ponndorf-Verley type reduction by computational technique. 相似文献
28.
Asymmetric Total Synthesis of Heronamides A–C: Stereochemical Confirmation and Impact of Long‐Range Stereochemical Communication on the Biological Activity
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Prof. Dr. Naoki Kanoh Shunya Itoh Kohei Fujita Dr. Kohei Sakanishi Ryosuke Sugiyama Yuta Terajima Prof. Dr. Yoshiharu Iwabuchi Prof. Dr. Shinichi Nishimura Prof. Dr. Hideaki Kakeya 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(25):8586-8595
Heronamides are biosynthetically related metabolites isolated from marine‐derived actinomycetes. Heronamide C shows potent antifungal activity by targeting membrane phospholipids possessing saturated hydrocarbon chains with as‐yet‐unrevealed modes of action. In spite of their curious hypothesized biosynthesis and fascinating biological activities, there have been conflicts in regard to the reported stereochemistries of heronamides. Here, we describe the asymmetric total synthesis of the originally proposed and revised structures of heronamide C, which unambiguously confirmed the chemical structure of this molecule. We also demonstrated nonenzymatic synthesis of heronamides A and B from heronamide C, which not only proved the postulated biosynthesis, but also confirmed the correct structures of heronamides A and B. Investigation of the structure–activity relationship of synthetic and natural heronamides revealed the importance of both long‐range stereochemical communication and the 20‐membered macrolactam ring for the biological activity of these compounds. 相似文献
29.
Noboru Ohtani Masakazu Katsuno Takashi Aigo Tatsuo Fujimoto Hiroshi Tsuge Hirokatsu Yashiro Masatoshi Kanaya 《Journal of Crystal Growth》2000,210(4):613-622
Surface topography of the {0 0 0 1} facet plane of as-grown 6H- and 4H-SiC crystals was studied ex situ by Nomarski optical microscopy (NOM) and atomic force microscopy (AFM). The surface polarity and the polytype of grown crystals largely affect the growth surface morphology of SiC{0 0 0 1} via differences in several thermodynamic and kinetic parameters. NOM observations revealed giant steps of a few micrometers in height on the {0 0 0 1} growth facet, and it was found that a morphological transition of the growth facet occurred when the growth conditions were changed. AFM imaging of the stepped structure of SiC{0 0 0 1} detected steps of height equal to the unit c-lattice parameter (c=1.512 nm for 6H-SiC and 1.005 nm for 4H-SiC). They are fairly straight and very regularly arranged, giving rise to equidistant step trains. Upon nitrogen doping, these regular step trains on the 6H-SiC(0 0 0
)C and 4H-SiC(0 0 0
)C surfaces became unstable: the equidistant step trains were transformed into meandering macrosteps of height greater than 10 nm. In this paper, we discuss the mechanism of macrostep formation (step bunching) on the SiC{0 0 0 1} surfaces through the consideration of the interplay between step energetics (repulsive step interaction) and kinetics (asymmetric step kinetics) on the growing crystal surface and elucidate how they affect the growth surface morphology of the SiC{0 0 0 1} facet. 相似文献
30.
Unusual Fragmentation Pathways in Collagen Glycopeptides 总被引:1,自引:0,他引:1
Irina Perdivara Lalith Perera Marnisa Sricholpech Masahiko Terajima Nancy Pleshko Mitsuo Yamauchi Kenneth B. Tomer 《Journal of the American Society for Mass Spectrometry》2013,24(7):1072-1081
Collagens are the most abundant glycoproteins in the body. One characteristic of this protein family is that the amino acid sequence consists of repeats of three amino acids –(X—Y—Gly)n. Within this motif, the Y residue is often 4-hydroxyproline (HyP) or 5-hydroxylysine (HyK). Glycosylation in collagen occurs at the 5-OH group in HyK in the form of two glycosides, galactosylhydroxylysine (Gal-HyK) and glucosyl galactosylhydroxylysine (GlcGal-HyK). In collision induced dissociation (CID), collagen tryptic glycopeptides exhibit unexpected gas-phase dissociation behavior compared to typical N- and O-linked glycopeptides (i.e., in addition to glycosidic bond cleavages, extensive cleavages of the amide bonds are observed). The Gal- or GlcGal- glycan modifications are largely retained on the fragment ions. These features enable unambiguous determination of the amino acid sequence of collagen glycopeptides and the location of the glycosylation site. This dissociation pattern was consistent for all analyzed collagen glycopeptides, regardless of their length or amino acid composition, collagen type or tissue. The two fragmentation pathways—amide bond and glycosidic bond cleavage—are highly competitive in collagen tryptic glycopeptides. The number of ionizing protons relative to the number of basic sites (i.e., Arg, Lys, HyK, and N-terminus) is a major driving force of the fragmentation. We present here our experimental results and employ quantum mechanics calculations to understand the factors enhancing the labile character of the amide bonds and the stability of hydroxylysine glycosides in gas phase dissociation of collagen glycopeptides.
Figure 相似文献